Cytogenetics tests in Dubai & UAE

Compare available Cytogenetics tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

Tests in this category

Listed price range

480.00–5,200.00 AED

Clinical preparation

Confirm test-specific instructions with your clinician or laboratory.

Compare available tests

Cytogenetics test prices

Showing 31–45 of 80 matching tests.

Cytogenetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-1148 FISH 1p/19q Codeletion Test This test detects the combined deletion of chromosome arms 1p and 19q in glioma tissue, a key diagnostic marker for oligodendroglioma.	Formalin-fixed paraffin-embedded (FFPE) tissue block	7 working days	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Deletion of chromosome arm 1p", "Deletion of chromosome arm 19q"] Parameters [] Preparation ["No patient preparation needed"] Indications ["Diagnosis of oligodendroglioma", "Prognosis determination in glioma", "Guiding chemotherapy response"] Measurement technique Confirm with laboratory Codes LOINC: 82463-9 ICD-10: C71.9, Z15.09, C71.1 Clinical summary This test detects the combined deletion of chromosome arms 1p and 19q in glioma tissue, a key diagnostic marker for oligodendroglioma.
TEST-1155 FISH Amniocentesis One Probe: Trisomy 21 (Down Syndrome) Test This diagnostic test evaluates amniotic fluid cells for the presence of an extra chromosome 21 (Trisomy 21) using FISH.	Amniotic fluid	4 days	650.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosome 21 copy number"] Parameters [] Preparation [] Indications ["Prenatal screening for Down syndrome after 15 weeks gestation", "High-risk pregnancy based on maternal age or ultrasound markers"] Measurement technique Confirm with laboratory Codes LOINC: 82120-6 ICD-10: Q90.9 Clinical summary This diagnostic test evaluates amniotic fluid cells for the presence of an extra chromosome 21 (Trisomy 21) using FISH.
TEST-1832 FISH BCL6 (3q27) Gene Rearrangement Test This test detects structural rearrangements of the BCL6 gene located on chromosome 3q27 using Fluorescence In Situ Hybridization (FISH). It is primarily used in the diagnosis and c...	Tissue (Fresh or FFPE tumour biopsy)	7–8 Business Days	1,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["BCL6 gene rearrangement", "Structural variants at 3q27 locus"] Parameters [] Preparation [] Indications ["Diffuse large B‑cell lymphoma", "Follicular lymphoma", "Other mature B‑cell neoplasms"] Measurement technique Confirm with laboratory Codes LOINC: 33556-8 ICD-10: C83.3 Clinical summary This test detects structural rearrangements of the BCL6 gene located on chromosome 3q27 using Fluorescence In Situ Hybridization (FISH). It is primarily used in the diagnosis and classification of B-cell lymphomas.
TEST-1136 FISH for 17p (TP53) Deletion Test This test detects the deletion of the TP53 gene on chromosome 17p using FISH on bone marrow aspirate.	Bone marrow aspirate	4 working days	950.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Deletion of TP53 gene", "Chromosome 17p abnormality"] Parameters [] Preparation ["Ensure the mandatory Chromosome & FISH analysis Requisition Form (Form 17) is fully completed and signed by your referring physician.", "No fasting or medication changes are required unless specifically instructed by your doctor."] Indications ["Diagnosis and prognosis of multiple myeloma", "Risk stratification in multiple myeloma"] Measurement technique Confirm with laboratory Codes LOINC: 76590-2 ICD-10: C90.00 Clinical summary This test detects the deletion of the TP53 gene on chromosome 17p using FISH on bone marrow aspirate.
TEST-1141 FISH for 22q11.2 Deletion (DiGeorge/VCFS) Test This diagnostic test evaluates for the presence of a microdeletion on chromosome 22q11.2, which is associated with DiGeorge syndrome (VCFS).	Peripheral whole blood (green-top sodium heparin tube)	4 working days	1,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Microdeletion on chromosome 22q11.2", "Presence of DiGeorge syndrome (VCFS) genetic marker"] Parameters [] Preparation ["No fasting required.", "Ensure child is hydrated and calm."] Indications ["Suspected DiGeorge syndrome (velocardiofacial syndrome)", "Infants/children with congenital heart defects", "Infants/children with hypocalcemia", "Infants/children with recurrent infections"] Measurement technique Confirm with laboratory Codes LOINC: 69342-5 ICD-10: Q93.81 Clinical summary This diagnostic test evaluates for the presence of a microdeletion on chromosome 22q11.2, which is associated with DiGeorge syndrome (VCFS).
TEST-1160 FISH for BCR-ABL1 Translocation (Philadelphia Chromosome) Test This diagnostic test evaluates for the presence of the BCR-ABL1 gene fusion, a specific chromosomal translocation associated with certain leukemias.	Peripheral blood or bone marrow aspirate	4 working days	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["BCR-ABL1 gene fusion", "t(9;22)(q34;q11.2) translocation"] Parameters [{"name": "BCR-ABL1 Fusion", "reference_range": "Negative"}] Preparation ["No specific fasting required.", "Inform the physician about all current medications, especially chemotherapy or TKIs."] Indications ["Suspected diagnosis of Chronic Myeloid Leukemia (CML)", "Suspected diagnosis of Philadelphia chromosome-positive Acute Lymphoblastic Leukemia (Ph+ ALL)", "Monitoring minimal residual disease (MRD) in CML or Ph+ ALL", "Assessing eligibility for tyrosine kinase inhibitor (TKI) therapy", "Evaluating treatment response"] Measurement technique Confirm with laboratory Codes LOINC: 33781-7 ICD-10: C92.10, C91.00 Clinical summary This diagnostic test evaluates for the presence of the BCR-ABL1 gene fusion, a specific chromosomal translocation associated with certain leukemias.
TEST-1173 FISH for Ewing Sarcoma (EWSR1 Rearrangement, 22q12) Test This diagnostic test evaluates formalin-fixed paraffin-embedded (FFPE) tissue for the presence of the EWSR1 gene rearrangement at 22q12 using fluorescence in-situ hybridization (FI...	Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Block	7–8 Working Days	1,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["EWSR1 gene rearrangement", "22q12 chromosomal locus"] Parameters [] Preparation [] Indications ["Suspicion of Ewing sarcoma", "Diagnosis of primitive neuroectodermal tumors", "Risk stratification", "Targeted therapy selection"] Measurement technique Confirm with laboratory Codes LOINC: 49490-4 ICD-10: C41.9 Clinical summary This diagnostic test evaluates formalin-fixed paraffin-embedded (FFPE) tissue for the presence of the EWSR1 gene rearrangement at 22q12 using fluorescence in-situ hybridization (FISH).
TEST-1181 FISH for HER2/neu Gene Amplification Test This diagnostic test evaluates the number of copies of the HER2 gene within tumor cells using fluorescence in-situ hybridization (FISH). It determines if the gene is amplified, ind...	Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Block / Archival Biopsy Specimen	10–12 business days	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["HER2 gene copy number", "HER2/CEP17 ratio"] Parameters [{"name": "HER2/CEP17 Ratio", "reference_range": "≥2.0 (Amplified), Preparation ["No patient preparation required; test performed on existing tissue samples."] Indications ["Diagnosis of breast cancer", "Diagnosis of gastric cancer", "Assessment for eligibility for anti-HER2 therapies (e.g., trastuzumab, pertuzumab)"] Measurement technique Confirm with laboratory Codes LOINC: 21630-8 ICD-10: C50.9, C16.9, Z51.0 Clinical summary This diagnostic test evaluates the number of copies of the HER2 gene within tumor cells using fluorescence in-situ hybridization (FISH). It determines if the gene is amplified, indicating potential responsiveness to anti-HER2 therapies.
TEST-1183 FISH for inv(16) / CBFB Gene Rearrangement Test This diagnostic test evaluates for the presence of inversions or translocations involving chromosome 16 and the CBFB gene, which are characteristic genetic markers for AML-M4Eo.	Whole blood (3 mL) or Bone marrow (2 mL)	4 working days	850.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["inv(16) chromosomal inversion", "CBFB gene rearrangement (break-apart or fusion)"] Parameters [] Preparation ["No fasting required", "Complete the mandatory Chromosome & FISH Analysis Requisition Form (Form 17)", "Sample must be collected in a sodium heparin green-top tube", "Sample must be kept at room temperature without freezing"] Indications ["Diagnosis of acute myeloid leukemia (AML)", "Subtyping of AML, specifically suspected AML-M4Eo", "Risk stratification in AML", "Guiding targeted therapy"] Measurement technique Confirm with laboratory Codes LOINC: 18022-7 ICD-10: C92.5 Clinical summary This diagnostic test evaluates for the presence of inversions or translocations involving chromosome 16 and the CBFB gene, which are characteristic genetic markers for AML-M4Eo.
TEST-1235 FISH for Monosomy 7 / del(7q31) Test This test detects the loss of chromosome 7 or deletion at the 7q31 region in blood or bone marrow cells.	Bone marrow aspirate or peripheral whole blood (sodium heparin)	4 working days from sample receipt	750.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Loss of chromosome 7 material", "Deletion at 7q31 locus"] Parameters [{"name": "Diagnostic Sensitivity for del(7q)/monosomy 7", "reference_range": "99.9 % analytical sensitivity"}] Preparation ["No specific dietary preparation required", "Inform clinical team if receiving anticoagulant therapy or have bleeding disorders"] Indications ["Diagnosis of Acute Myeloid Leukaemia (AML)", "Diagnosis of Myelodysplastic Syndromes (MDS)", "Risk stratification in AML/MDS"] Measurement technique Confirm with laboratory Codes LOINC: 82195-0 ICD-10: C92.00, D46.9 Clinical summary This test detects the loss of chromosome 7 or deletion at the 7q31 region in blood or bone marrow cells.
TEST-1193 FISH for Multiple Myeloma with CD138 Positive Selection (Bone Marrow) Test This diagnostic test evaluates bone marrow plasma cells for specific chromosomal abnormalities associated with multiple myeloma using Fluorescence In Situ Hybridization (FISH) afte...	Bone Marrow Aspirate	4 Working Days	2,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal abnormalities (e.g., del(17p), t(4;14), t(14;16), gain of 1q)", "Plasma cell purity"] Parameters [{"name": "Plasma Cell Purity", "reference_range": ">95% via immunomagnetic CD138 enrichment"}, {"name": "Detection Sensitivity", "reference_range": "Identifies abnormalities in as few as 1% of cells"}] Preparation ["Sign consent form", "Avoid anticoagulant medications as advised by doctor", "Complete Chromosome & FISH analysis Requisition Form (Form 17)"] Indications ["Diagnosis of multiple myeloma", "Risk stratification in multiple myeloma", "Prognosis determination", "Treatment planning"] Measurement technique Confirm with laboratory Codes LOINC: 97918-9 ICD-10: C90.0 Clinical summary This diagnostic test evaluates bone marrow plasma cells for specific chromosomal abnormalities associated with multiple myeloma using Fluorescence In Situ Hybridization (FISH) after CD138 positive selection.
TEST-498 FISH for Prenatal and Postnatal Diagnosis of Chromosomes 18, X, and Y Test This diagnostic test evaluates for the presence of specific numerical chromosomal abnormalities (aneuploidies) involving chromosomes 18, X, and Y using Fluorescence In-Situ Hybridi...	Prenatal (Amniotic Fluid, Chorionic Villus) / Postnatal (Peripheral Blood)	10–12 Days	900.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Numerical abnormalities of chromosome 18", "Numerical abnormalities of chromosome X", "Numerical abnormalities of chromosome Y"] Parameters [] Preparation [] Indications ["Prenatal screening for suspected aneuploidies (Trisomy 18, Turner syndrome, Klinefelter syndrome)", "Postnatal diagnosis of suspected aneuploidies", "Rapid assessment of chromosomal status when conventional karyotyping is too slow"] Measurement technique Confirm with laboratory Codes LOINC: 32702-7 ICD-10: Z36.0 Clinical summary This diagnostic test evaluates for the presence of specific numerical chromosomal abnormalities (aneuploidies) involving chromosomes 18, X, and Y using Fluorescence In-Situ Hybridization.
TEST-474 FISH for Prenatal/Postnatal Diagnosis Chromosomes 13 and 23 Test This diagnostic test evaluates for the presence of trisomy 13 (Patau syndrome) and common sex chromosome aneuploidies (e.g., Turner syndrome, Klinefelter syndrome) using Fluorescen...	Amniotic Fluid, Chorionic Villus Sample, Peripheral Blood	10–12 days	900.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosome 13 copy number", "Sex chromosome (X and Y) copy number", "Presence of aneuploidies (trisomy 13, sex chromosome anomalies)"] Parameters [{"name": "Trisomy 13", "reference_range": "Negative"}, {"name": "Sex Chromosome Aneuploidy (X, Y)", "reference_range": "Normal"}] Preparation ["Sign prenatal genetic testing consent form (Form 18)", "Sign chromosome and FISH analysis requisition form (Form 17)"] Indications ["Prenatal screening for trisomy 13 and sex chromosome aneuploidies", "Postnatal diagnosis of suspected chromosomal abnormalities", "Rapid assessment in high-risk pregnancies"] Measurement technique Confirm with laboratory Codes LOINC: 21857-0 ICD-10: Z13.79, Q91.4, Q96.9, Q97.9, Q98.9 Clinical summary This diagnostic test evaluates for the presence of trisomy 13 (Patau syndrome) and common sex chromosome aneuploidies (e.g., Turner syndrome, Klinefelter syndrome) using Fluorescence In-Situ Hybridization (FISH).
TEST-493 FISH for Trisomy 13 (Patau Syndrome) Test This diagnostic test evaluates the number of copies of chromosome 13 in fetal or neonatal cells using FISH.	Amniotic fluid, cord blood, neonatal peripheral blood	5–7 working days	750.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosome 13 copy number", "Aneuploidy detection for chromosome 13"] Parameters [] Preparation [] Indications ["Prenatal screening results suggesting high risk for Trisomy 13", "Abnormal ultrasound findings suggestive of Trisomy 13", "Neonatal presentation consistent with Patau syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 49582-8 ICD-10: Q91.4, Q91.5, Q91.6, Q91.7 Clinical summary This diagnostic test evaluates the number of copies of chromosome 13 in fetal or neonatal cells using FISH.
TEST-1247 FISH for Trisomy 21 (Down Syndrome) Test This diagnostic test evaluates fetal cells for the presence of an extra chromosome 21, confirming or ruling out Trisomy 21 (Down syndrome).	Amniotic fluid, Chorionic villus (CVS), Cord blood	4 days	750.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosome 21 copy number"] Parameters [] Preparation [] Indications ["Positive prenatal screening test", "Advanced maternal age", "Family history of chromosomal abnormalities", "Ultrasound findings suggestive of aneuploidy"] Measurement technique Confirm with laboratory Codes LOINC: 53177-3 ICD-10: Q90.0, Q90.9, Z36.0 Clinical summary This diagnostic test evaluates fetal cells for the presence of an extra chromosome 21, confirming or ruling out Trisomy 21 (Down syndrome).

Category overview

Cytogenetics: overview

Understanding your genetic blueprint can provide invaluable clarity for both proactive health planning and specialized medical care. The Cytogenetics division at DNA Labs UAE employs cutting-edge chromosomal microarray and FISH technologies to analyze cellular genetics. Whether assessing hereditary conditions or guiding specialized treatments, our advanced cytogenetic testing in the UAE acts as a critical navigational tool for your physician. Ranked among the top diagnostic labs in Dubai/UAE, we handle your sensitive genetic data with absolute confidentiality, ensuring you receive fast, precise, and secure results. Empower your medical decisions. Browse our cytogenetics services below, arrange a private home collection, or speak with our genetics specialists today.

Before booking

Use the test details as a conversation starter

The right diagnostic option depends on your reason for testing and individual circumstances. Check the listed specimen and timing, then confirm any preparation requirements with the ordering clinician or laboratory before collection.

Explore this area

Cytogenetics tests in Dubai & UAE

Cytogenetics test prices

Cytogenetics: overview

Use the test details as a conversation starter

Related Cytogenetics categories