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.

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480.00–5,200.00 AED

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Cytogenetics test prices

Showing 46–60 of 80 matching tests.

Cytogenetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-1192 FISH Microdeletion Detection for Williams Syndrome Test This test detects the specific microdeletion on chromosome 7q11.23 associated with Williams syndrome.	Peripheral whole blood	4 working days	1,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Deletion of the ELN gene", "Chromosome 7q11.23 region"] Parameters [] Preparation [] Indications ["Suspected Williams syndrome based on clinical presentation", "Neonatal or paediatric patients with relevant symptoms"] Measurement technique Confirm with laboratory Codes LOINC: 33914-3 ICD-10: Q93.81 Clinical summary This test detects the specific microdeletion on chromosome 7q11.23 associated with Williams syndrome.
TEST-1202 FISH Opposite Sex Bone Marrow Transplant (XX/XY) Test This diagnostic test evaluates the percentage of donor cells with opposite-sex chromosomes (XX or XY) in a post-bone marrow transplant patient.	Bone Marrow Aspirate or Peripheral Whole Blood (Green-top Sodium Heparin Tube)	4 Working Days	750.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Donor cell engraftment", "Chimerism"] Parameters [] Preparation ["No fasting required", "Inform phlebotomist of recent blood transfusions", "Complete Chromosome & FISH Analysis Requisition Form (Form 17)"] Indications ["Post-opposite-sex bone marrow transplant monitoring", "Assessment of engraftment success"] Measurement technique Confirm with laboratory Codes LOINC: 44508-3 ICD-10: Z94.8 Clinical summary This diagnostic test evaluates the percentage of donor cells with opposite-sex chromosomes (XX or XY) in a post-bone marrow transplant patient.
TEST-1215 FISH Postnatal Gender Confirmation Test This test rapidly determines the number of X and Y chromosomes in a blood sample to confirm genetic sex.	Peripheral Whole Blood	4 Business Days	750.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["X chromosome copy number", "Y chromosome copy number"] Parameters [{"name": "X Chromosome Copy Number", "reference_range": "1 or 2"}, {"name": "Y Chromosome Copy Number", "reference_range": "0 or 1"}] Preparation ["No specific fasting or dietary restrictions required", "Inform clinical team if child has a known bleeding disorder or is receiving anticoagulant therapy"] Indications ["Evaluation of newborns with ambiguous genitalia", "Suspected Turner syndrome (45,X)", "Suspected Klinefelter syndrome (47,XXY)", "Rapid genetic assessment in neonatal period"] Measurement technique Confirm with laboratory Codes LOINC: 49005-3 ICD-10: Z13.79, Q56.4, Q98.8 Clinical summary This test rapidly determines the number of X and Y chromosomes in a blood sample to confirm genetic sex.
TEST-1212 FISH Prenatal Screening Panel (Chromosomes 13, 18, 21, X & Y) Test This diagnostic test evaluates amniotic fluid cells for the presence of common chromosomal aneuploidies (trisomy 13, 18, 21, and sex chromosome abnormalities) using FISH.	Amniotic Fluid	4 Days (Report by 4 pm)	1,400.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosome 13 copy number", "Chromosome 18 copy number", "Chromosome 21 copy number", "X chromosome copy number", "Y chromosome copy number"] Parameters [] Preparation [] Indications ["High-risk non-invasive prenatal testing (NIPT) results", "Advanced maternal age (≥35 years)", "Ultrasound markers suggestive of aneuploidy"] Measurement technique Confirm with laboratory Codes LOINC: 82121-9 ICD-10: Z36.0 Clinical summary This diagnostic test evaluates amniotic fluid cells for the presence of common chromosomal aneuploidies (trisomy 13, 18, 21, and sex chromosome abnormalities) using FISH.
TEST-1229 FISH ROS1 (6q22) Rearrangement Test This test detects rearrangements in the ROS1 gene within tumour tissue using FISH.	Archival Tissue Specimen (FFPE Block or Unstained Slides)	4 Working Days	1,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ROS1 gene rearrangement", "Break-apart signals"] Parameters [] Preparation [] Indications ["Diagnosis of ROS1-positive non-small cell lung cancer", "Identification of patients eligible for ROS1 targeted therapy"] Measurement technique Confirm with laboratory Codes LOINC: 94272-8 ICD-10: C34.9 Clinical summary This test detects rearrangements in the ROS1 gene within tumour tissue using FISH.
TEST-1242 FISH t(11;14) (LSI IGH/CCND1) Test This test identifies the presence of the t(11;14) chromosomal translocation, a genetic marker associated with specific types of lymphoma.	Peripheral Blood (5 mL) or Bone Marrow (4 mL)	4 Working Days	750.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal translocation t(11;14)", "IGH/CCND1 gene fusion"] Parameters [] Preparation ["No fasting required", "Inform doctor of all medications", "Complete Chromosome & FISH Requisition Form (Form 17)"] Indications ["Suspected mantle cell lymphoma", "Diagnosis of B-cell lymphomas", "Prognostic assessment"] Measurement technique Confirm with laboratory Codes LOINC: 33632-7 ICD-10: C83.1 Clinical summary This test identifies the presence of the t(11;14) chromosomal translocation, a genetic marker associated with specific types of lymphoma.
TEST-1238 FISH t(12;21) (TEL/AML1) Test This diagnostic test evaluates for the presence of the t(12;21) chromosomal translocation, specifically the ETV6-RUNX1 gene fusion, in blood or bone marrow cells.	Whole blood (sodium heparin – green top) or bone marrow aspirate	4 working days	750.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["ETV6-RUNX1 gene fusion", "t(12;21)(p13;q22) translocation"] Parameters [] Preparation ["No specific patient preparation required", "Ensure sample collection follows protocol (sodium heparin or bone marrow)"] Indications ["Diagnosis of B-cell acute lymphoblastic leukemia (B-ALL)", "Prognostic stratification in B-ALL", "Monitoring minimal residual disease (MRD)"] Measurement technique Confirm with laboratory Codes LOINC: 34973-7 ICD-10: C91.00 Clinical summary This diagnostic test evaluates for the presence of the t(12;21) chromosomal translocation, specifically the ETV6-RUNX1 gene fusion, in blood or bone marrow cells.
TEST-1138 FISH t(8;21) (LSI ETO/AML1) Translocation Test This test detects the presence of the t(8;21) chromosomal translocation, a specific genetic marker associated with a subtype of Acute Myeloid Leukemia (AML).	Bone Marrow Aspirate (2 mL) or Peripheral Whole Blood (5 mL)	4 Working Days (report by 6 PM)	750.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["RUNX1-RUNX1T1 (AML1-ETO) fusion gene", "t(8;21) translocation"] Parameters [] Preparation ["Disclose all anticoagulant use (aspirin, warfarin, clopidogrel) to your doctor 3-5 days before bone marrow collection.", "No fasting required for peripheral blood collection.", "Avoid strenuous exercise 6 hours prior to peripheral blood collection.", "A duly filled Chromosome & FISH Analysis Requisition Form (Form 17) is mandatory."] Indications ["Diagnosis of Acute Myeloid Leukemia (AML)", "Prognostic evaluation in AML", "Risk stratification for AML treatment"] Measurement technique Confirm with laboratory Codes LOINC: 40433-4 ICD-10: C92.0 Clinical summary This test detects the presence of the t(8;21) chromosomal translocation, a specific genetic marker associated with a subtype of Acute Myeloid Leukemia (AML).
TEST-1133 FISH Test This diagnostic test evaluates for the presence of the t(8;14) translocation between the MYC and IGH genes in blood or bone marrow cells.	5 mL whole blood (Sodium Heparin, Green Top) or 4 mL bone marrow	4 working days from sample receipt	750.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MYC/IGH gene translocation", "Presence of specific chromosomal rearrangement"] Parameters [{"name": "MYC/IGH fusion", "reference_range": ">99% sensitivity"}] Preparation ["No fasting required for peripheral blood sampling", "Disclose all anticoagulant or antiplatelet medications to your haematologist at least 48 hours prior to bone marrow aspiration"] Indications ["Diagnosis of Burkitt lymphoma", "Diagnosis of aggressive B‑cell non‑Hodgkin lymphomas", "Confirmation of suspected MYC/IGH translocation"] Measurement technique Confirm with laboratory Codes LOINC: 48756-3 ICD-10: C83.7, C83.3 Clinical summary This diagnostic test evaluates for the presence of the t(8;14) translocation between the MYC and IGH genes in blood or bone marrow cells.
TEST-1222 FISH Test for Synovial Sarcoma (SS18/SYT) 18q11.2 Gene Rearrangement This diagnostic test evaluates for the presence of the SS18 (SYT) gene rearrangement at chromosomal locus 18q11.2, which is characteristic of synovial sarcoma.	Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Block	4 Working Days	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SS18 (SYT) gene rearrangement", "Chromosomal locus 18q11.2"] Parameters [] Preparation ["No special preparation is needed by the patient."] Indications ["Suspicion of synovial sarcoma", "Differentiation from other soft-tissue neoplasms", "Guiding targeted therapy"] Measurement technique Confirm with laboratory Codes LOINC: 90553-7 ICD-10: C49.9 Clinical summary This diagnostic test evaluates for the presence of the SS18 (SYT) gene rearrangement at chromosomal locus 18q11.2, which is characteristic of synovial sarcoma.
TEST-505 FISH Trisomy 18 (Edwards Syndrome) Test This diagnostic test evaluates for the presence of an extra copy of chromosome 18 (Trisomy 18) in fetal cells.	Amniotic fluid, peripheral blood, or bone marrow aspirate	5–7 working days	750.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosome 18 copy number", "Presence of trisomy 18"] Parameters [] Preparation ["Submit completed Chromosome & FISH Analysis Requisition Form (Form 17)", "Submit signed Prenatal Genetic Testing Consent Form (Form 18)"] Indications ["Prenatal screening indicating high risk for Trisomy 18", "Confirmation of suspected Edwards syndrome", "Rapid diagnosis needed for pregnancy management"] Measurement technique Confirm with laboratory Codes LOINC: 82121-4 ICD-10: Q91.0, Q91.1, Q91.2 Clinical summary This diagnostic test evaluates for the presence of an extra copy of chromosome 18 (Trisomy 18) in fetal cells.
TEST-1251 FISH‑NTRK1/2/3 Gene Fusion Panel Test This test detects the presence of NTRK1, NTRK2, or NTRK3 gene fusions in solid tumor tissue using Fluorescence In-Situ Hybridisation (FISH). It helps determine eligibility for targ...	FFPE Tissue Blocks or Slides (Archival Solid Tissue Specimen)	4 Working Days	2,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["NTRK1 gene rearrangements", "NTRK2 gene rearrangements", "NTRK3 gene rearrangements"] Parameters [] Preparation [] Indications ["Solid tumors where fusion status determines eligibility for histology-agnostic treatment"] Measurement technique Confirm with laboratory Codes LOINC: 101418-6 ICD-10: Z85.9 Clinical summary This test detects the presence of NTRK1, NTRK2, or NTRK3 gene fusions in solid tumor tissue using Fluorescence In-Situ Hybridisation (FISH). It helps determine eligibility for targeted therapies like TRK inhibitors.
TEST-1170 FISH, 13q14.3 (D13S319) Deletion Test This diagnostic test evaluates the presence or absence of a specific deletion (del(13q14.3)) in the chromosomes of a patient's cells, primarily bone marrow or peripheral blood.	Bone marrow aspirate or peripheral blood (Green Top-Heparin)	4 Business Days	850.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Deletion of the 13q14.3 chromosomal region", "Presence of the D13S319 locus"] Parameters [] Preparation ["Avoid aspirin, clopidogrel, warfarin, or other anticoagulants/antiplatelet agents for the period specified by your physician prior to bone marrow collection.", "Stop herbal supplements such as Ginkgo biloba and high-dose Vitamin E 7 days before the procedure."] Indications ["Diagnosis and risk stratification of Multiple Myeloma", "Prognostic assessment in Multiple Myeloma"] Measurement technique Confirm with laboratory Codes LOINC: 49595-5 ICD-10: C90.0 Clinical summary This diagnostic test evaluates the presence or absence of a specific deletion (del(13q14.3)) in the chromosomes of a patient's cells, primarily bone marrow or peripheral blood.
TEST-1241 High-Resolution Couple Karyotyping Test This test evaluates the number and structure of chromosomes in both partners to identify abnormalities linked to reproductive health issues.	Peripheral whole blood (two samples, one per partner)	10–12 working days	1,900.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal structure", "Chromosomal number", "Presence of translocations", "Presence of inversions", "Presence of aneuploidy"] Parameters [{"name": "Resolution", "reference_range": "550–850 bands per haploid set"}] Preparation ["No specific fasting required", "Continue all prescribed medications unless advised otherwise by your physician"] Indications ["Investigation of infertility", "Evaluation of recurrent pregnancy loss", "Preconception screening for chromosomal abnormalities", "Assessment of hereditary cancer predisposition"] Measurement technique Confirm with laboratory Codes LOINC: 18479-5 ICD-10: Z31.5 Clinical summary This test evaluates the number and structure of chromosomes in both partners to identify abnormalities linked to reproductive health issues.
TEST-629 High‑Resolution Neonatal Chromosome Analysis (Karyotyping) Test This test evaluates the number and structure of chromosomes in a newborn's cells.	Peripheral whole blood	21 working days	480.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Numerical chromosome abnormalities (e.g., trisomies, monosomies)", "Structural chromosome abnormalities (e.g., deletions, duplications, translocations)"] Parameters [] Preparation [] Indications ["Suspected chromosomal syndrome", "Congenital disorders", "Birth defects"] Measurement technique Confirm with laboratory Codes LOINC: 34523-4 ICD-10: Z13.71, Z13.79 Clinical summary This test evaluates the number and structure of chromosomes in a newborn's cells.

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.

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Cytogenetics tests in Dubai & UAE

Cytogenetics test prices

Cytogenetics: overview

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