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 1–15 of 80 matching tests.

Cytogenetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-1656 17p (TP53) Deletion FISH Test for Multiple Myeloma & CLL This test detects the loss of the TP53 gene on chromosome 17p, a key prognostic marker in multiple myeloma and CLL.	Bone Marrow Aspirate or Peripheral Blood (EDTA)	3–4 working days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Loss of TP53 gene locus on chromosome 17p", "Percentage of cells with 17p deletion"] Parameters [{"name": "Percentage of nuclei with 17p deletion", "reference_range": " Preparation ["No fasting required", "Inform phlebotomist of any anticoagulant therapy"] Indications ["Risk stratification in Multiple Myeloma (MM)", "Risk stratification in Chronic Lymphocytic Leukaemia (CLL)", "Guiding therapy selection in MM and CLL"] Measurement technique Confirm with laboratory Codes LOINC: 33729-6 ICD-10: C90.0, C91.1 Clinical summary This test detects the loss of the TP53 gene on chromosome 17p, a key prognostic marker in multiple myeloma and CLL.
TEST-1867 ALL FISH Panel (Acute Lymphoblastic Leukemia) Test This test detects specific chromosomal rearrangements (BCR::ABL1, ETV6::RUNX1, KMT2A, TCF3) associated with Acute Lymphoblastic Leukemia (ALL).	Bone marrow aspirate (preferred) or peripheral blood	10 calendar days	2,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["BCR::ABL1 rearrangement", "ETV6::RUNX1 rearrangement", "KMT2A rearrangement", "TCF3 rearrangement"] Parameters [] Preparation ["No fasting required", "No medication avoidance required solely for the FISH procedure", "Follow doctor’s specific preparation instructions"] Indications ["Diagnosis of suspected or confirmed acute lymphoblastic leukemia", "Risk stratification in ALL", "Guiding therapy selection in ALL", "Monitoring minimal residual disease (MRD)"] Measurement technique Confirm with laboratory Codes LOINC: 100358-2 ICD-10: C91.0 Clinical summary This test detects specific chromosomal rearrangements (BCR::ABL1, ETV6::RUNX1, KMT2A, TCF3) associated with Acute Lymphoblastic Leukemia (ALL).
TEST-508 Amniotic Fluid Molecular Karyotyping Test This diagnostic test evaluates fetal chromosomes from amniotic fluid for structural and numerical abnormalities, including microdeletions and duplications.	Amniotic Fluid	7–9 Business Days	2,100.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal Copy Number Variants (CNVs)", "Aneuploidies", "Microdeletions", "Microduplications"] Parameters [] Preparation ["Medication review prior to procedure", "Avoid aspirin, anticoagulants, antiplatelet drugs, or immunosuppressants if possible"] Indications ["Advanced maternal age", "Abnormal ultrasound findings", "Positive prenatal screening results", "Family history of genetic disorders", "Previous child with chromosomal abnormalities"] Measurement technique Confirm with laboratory Codes LOINC: 81272-4 ICD-10: Z36.8 Clinical summary This diagnostic test evaluates fetal chromosomes from amniotic fluid for structural and numerical abnormalities, including microdeletions and duplications.
TEST-1163 BCL6 (3q27) Gene Rearrangement Test This test detects chromosomal translocations involving the BCL6 gene on chromosome 3q27, which are characteristic of certain aggressive B-cell lymphomas.	Bone marrow aspirate or tissue biopsy	4 working days	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal translocation involving 3q27 locus", "BCL6 gene rearrangement"] Parameters [] Preparation ["Do not discontinue prescribed medication without consulting your doctor.", "A completed Chromosome & FISH Requisition Form (Form 17) is mandatory."] Indications ["Diagnostic workup of aggressive B-cell lymphomas", "Confirmation of diffuse large B-cell lymphoma (DLBCL)", "Evaluation of follicular lymphoma", "Assessment of high-grade B-cell lymphoma"] Measurement technique Confirm with laboratory Codes LOINC: 68299-1 ICD-10: C83.3 Clinical summary This test detects chromosomal translocations involving the BCL6 gene on chromosome 3q27, which are characteristic of certain aggressive B-cell lymphomas.
TEST-1831 BCR-ABL (CML/AML/ALL) FISH Test This test detects the BCR-ABL1 gene fusion, a key marker for Chronic Myeloid Leukemia (CML), Philadelphia-positive Acute Lymphoblastic Leukemia (ALL), and certain AML subtypes.	Peripheral Blood or Bone Marrow Aspirate	3–4 working days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["BCR-ABL1 gene fusion", "t(9;22) translocation"] Parameters [] Preparation ["Fasting is not required", "Inform phlebotomist about anti-coagulant or anti-platelet medications"] Indications ["Diagnosis of CML", "Diagnosis of Philadelphia-positive ALL", "Diagnosis of certain AML subtypes", "Monitoring response to TKI therapy", "Minimal residual disease (MRD) assessment"] Measurement technique Confirm with laboratory Codes LOINC: 34984-3 ICD-10: C92.1, C91.0, C92.0 Clinical summary This test detects the BCR-ABL1 gene fusion, a key marker for Chronic Myeloid Leukemia (CML), Philadelphia-positive Acute Lymphoblastic Leukemia (ALL), and certain AML subtypes.
TEST-2159 Breast Comprehensive Panel Genetic Test This test evaluates 30 genes for germline variants associated with increased risk of hereditary breast, ovarian, and related cancers.	Whole Blood (EDTA), Extracted DNA, or One-Drop Blood on FTA Card	3 to 4 Weeks (Includes Confirmatory Orthogonal Validation)	3,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic germline variants", "Hereditary cancer susceptibility"] Parameters [{"name": "Genes Analyzed", "reference_range": "30 Genes (ABRAXAS1, ATM, BARD1, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, DICER1, EPCAM, FANCC, MEN1, MLH1, MRE11, MSH2, MSH6, MUTYH, NBN, PALB2, PMS1, PMS2, PTEN, RAD50, RAD51C, RAD51D, RECQL, SMARCA4, STK11, TP53, XRCC2)"}] Preparation ["No fasting required", "No medication adjustments required", "Inform laboratory if patient has undergone allogeneic bone marrow transplantation", "Complete and submit clinical history form"] Indications ["Personal history of early-onset breast cancer (diagnosed before age 50)", "Personal history of triple-negative breast cancer", "Personal history of bilateral breast cancer", "Personal history of ovarian cancer at any age", "Personal history of male breast cancer", "Strong family history of breast, ovarian, pancreatic, or aggressive prostate cancer", "Ashkenazi Jewish ancestry", "Known familial pathogenic variant"] Measurement technique Confirm with laboratory Codes LOINC: 96783-1 ICD-10: Z15.01, Z13.820 Clinical summary This test evaluates 30 genes for germline variants associated with increased risk of hereditary breast, ovarian, and related cancers.
TEST-1700 C-Myc (MYC) Gene Rearrangement by FISH Test This test detects rearrangements of the MYC gene, which are associated with certain types of leukemia and lymphoma.	Bone marrow aspirate (primary) / peripheral blood (alternative)	3–4 working days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MYC gene translocations (8q24)", "Chromosomal rearrangements"] Parameters [] Preparation ["Inform doctor about anticoagulant or antiplatelet medications"] Indications ["Diagnosis of acute lymphoblastic leukemia (ALL)", "Diagnosis of non-Hodgkin lymphoma (NHL)", "Diagnosis of Burkitt lymphoma", "Classification of diffuse large B-cell lymphoma"] Measurement technique Confirm with laboratory Codes LOINC: 48767-5 ICD-10: C91.00, C83.70, C83.39 Clinical summary This test detects rearrangements of the MYC gene, which are associated with certain types of leukemia and lymphoma.
TEST-1164 C‑MYC Amplification (FISH Test) This test detects the amplification (extra copies) of the MYC oncogene in blood or bone marrow cells using FISH.	Peripheral whole blood (sodium heparin) or bone marrow aspirate	4 days	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["MYC gene copy number", "MYC amplification"] Parameters [] Preparation ["No fasting required", "Inform clinical team about all current medications, allergies, and any bleeding disorders"] Indications ["Diagnosis of aggressive B-cell lymphomas", "Risk stratification in lymphoma", "WHO classification"] Measurement technique Confirm with laboratory Codes LOINC: 49568-2 ICD-10: C85.90 Clinical summary This test detects the amplification (extra copies) of the MYC oncogene in blood or bone marrow cells using FISH.
TEST-524 Cancer Breast Comprehensive Panel Test This diagnostic test evaluates key biomarkers in breast tissue to determine hormone receptor status, HER2 amplification, Ki-67 proliferation index, and microsatellite instability.	Archival Tissue – Formalin-fixed paraffin-embedded (FFPE) tissue block or slides	10 working days	2,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Estrogen Receptor (ER)", "Progesterone Receptor (PR)", "HER2 Protein Expression", "HER2 Gene Amplification", "Ki-67 Proliferation Index", "Microsatellite Instability (MSI)"] Parameters [{"name": "Estrogen Receptor (ER)", "reference_range": null}, {"name": "Progesterone Receptor (PR)", "reference_range": null}, {"name": "HER2 (IHC)", "reference_range": null}, {"name": "HER2 (FISH)", "reference_range": null}, {"name": "Ki-67", "reference_range": null}, {"name": "Microsatellite Instability (MSI)", "reference_range": null}] Preparation [] Indications ["Diagnosis of breast cancer", "Prognosis assessment", "Guidance for targeted therapy selection"] Measurement technique Confirm with laboratory Codes LOINC: 74774-5 ICD-10: C50.9 Clinical summary This diagnostic test evaluates key biomarkers in breast tissue to determine hormone receptor status, HER2 amplification, Ki-67 proliferation index, and microsatellite instability.
TEST-1736 CCND1 FISH Gene Amplification Test This diagnostic test evaluates the presence and degree of amplification of the CCND1 gene (cyclin D1) within tumour tissue using Fluorescence In-Situ Hybridization (FISH).	Tumour tissue (biopsy / archival FFPE block)	7–8 days	1,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CCND1 gene amplification", "Cyclin D1 oncogene copy number"] Parameters [] Preparation ["A valid physician’s prescription is required, except for surgical cases, pregnancy, or international travel.", "No special preparation (fasting/diet) is needed."] Indications ["Diagnosis of mantle cell lymphoma", "Classification of certain breast cancers", "Risk stratification of plasma cell myeloma", "Guiding targeted therapy decisions"] Measurement technique Confirm with laboratory Codes LOINC: 86163-6 ICD-10: C83.1, C50.919, Z15.01 Clinical summary This diagnostic test evaluates the presence and degree of amplification of the CCND1 gene (cyclin D1) within tumour tissue using Fluorescence In-Situ Hybridization (FISH).
TEST-1738 CCND1 Gene FISH Test This test detects the t(11;14) translocation, a genetic marker for mantle cell lymphoma.	Bone Marrow Aspirate or Peripheral Blood	3–4 business days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["t(11;14) translocation", "Cyclin D1 gene rearrangement"] Parameters [] Preparation ["No fasting required", "Valid physician’s prescription needed"] Indications ["Suspected mantle cell lymphoma", "Differentiation of B-cell lymphomas"] Measurement technique Confirm with laboratory Codes LOINC: 52004-6 ICD-10: C83.1 Clinical summary This test detects the t(11;14) translocation, a genetic marker for mantle cell lymphoma.
TEST-634 Chromosome Analysis (Amniotic Fluid) Test This diagnostic test evaluates fetal cells obtained from amniotic fluid for numerical and structural chromosomal abnormalities using karyotyping.	Amniotic Fluid	21 Working Days	1,900.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Fetal Chromosomes", "Numerical Chromosomal Abnormalities (Aneuploidies)", "Structural Chromosomal Abnormalities (Translocations, Deletions)"] Parameters [] Preparation ["Inform physician of all medications, supplements, and herbal products.", "Anticoagulants, antiplatelet drugs, and certain antibiotics may need adjustment.", "Do not stop any treatment without explicit medical guidance."] Indications ["Advanced maternal age", "Abnormal prenatal screening results (e.g., NIPT, Quad Screen)", "Abnormal ultrasound findings", "Family history of chromosomal abnormalities", "Previous child with chromosomal abnormalities"] Measurement technique Confirm with laboratory Codes LOINC: 17852-2 ICD-10: Z36.2 Clinical summary This diagnostic test evaluates fetal cells obtained from amniotic fluid for numerical and structural chromosomal abnormalities using karyotyping.
TEST-625 Chromosome Analysis (Philadelphia) Test This diagnostic test evaluates the chromosomes in bone marrow cells to detect the presence of the Philadelphia chromosome (BCR-ABL1 fusion gene).	Bone Marrow Aspirate	7 Working Days	650.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["BCR-ABL1 fusion gene", "Chromosomal abnormalities", "Karyotype"] Parameters [] Preparation ["No specific patient preparation required", "Inform physician about current medications"] Indications ["Diagnosis of Chronic Myeloid Leukemia (CML)", "Diagnosis of Philadelphia-positive Acute Lymphoblastic Leukemia (ALL)", "Risk stratification in leukemia", "Monitoring treatment response"] Measurement technique Confirm with laboratory Codes LOINC: 33774-5 ICD-10: C92.10, C91.00 Clinical summary This diagnostic test evaluates the chromosomes in bone marrow cells to detect the presence of the Philadelphia chromosome (BCR-ABL1 fusion gene).
TEST-620 Chromosome Analysis (Solid Tumor) Test This diagnostic test evaluates the chromosomal makeup of solid tumor cells using conventional karyotyping.	Solid Tumor Tissue (Viable, Fresh)	21 working days	1,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal abnormalities (translocations, aneuploidy, deletions, marker chromosomes)", "Clonal chromosomal aberrations"] Parameters [] Preparation [] Indications ["Oncological diagnosis", "Prognosis determination", "Targeted therapy selection", "Characterization of solid malignancies"] Measurement technique Confirm with laboratory Codes LOINC: 62364-5 ICD-10: Z15.09, C80.1, Z85.9 Clinical summary This diagnostic test evaluates the chromosomal makeup of solid tumor cells using conventional karyotyping.
TEST-622 Chromosome Analysis of Products of Conception with Reflex FISH for Aneuploidy Detection Test This test evaluates the chromosomal constitution of products of conception to detect aneuploidies, a common cause of early pregnancy loss.	Products of Conception (POC) – Fresh Curretted Villous Tissue in Sterile Normal Saline	4–5 weeks	1,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal number (aneuploidy)", "Structural chromosomal abnormalities"] Parameters [] Preparation [] Indications ["Investigation of spontaneous abortion", "Evaluation of missed abortion", "Recurrent pregnancy loss workup"] Measurement technique Confirm with laboratory Codes LOINC: 69181-3 ICD-10: O03.9, O02.1 Clinical summary This test evaluates the chromosomal constitution of products of conception to detect aneuploidies, a common cause of early pregnancy loss.

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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