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 16–30 of 80 matching tests.

Cytogenetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-1729 Chromosome Breakage Syndrome Test This diagnostic test evaluates the stability of chromosomes under stress, identifying increased fragility indicative of specific genetic syndromes.	Peripheral blood	8–10 business days	1,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal fragility", "Response to DNA damaging agents (Mitomycin C, Diepoxybutane)"] Parameters [] Preparation ["Avoid test ≥ 4 weeks after chemotherapy, radiotherapy, or bone marrow transplant.", "Inform lab if patient has severe leucopenia (WBC < 2.0 ×10⁹/L)."] Indications ["Suspected Fanconi anemia", "Diagnosis of other chromosome instability syndromes", "Evaluation of inherited bone marrow failure"] Measurement technique Confirm with laboratory Codes LOINC: 59083-1 ICD-10: D61.0 Clinical summary This diagnostic test evaluates the stability of chromosomes under stress, identifying increased fragility indicative of specific genetic syndromes.
TEST-623 Chromosome XON Microarray High Resolution Test This test evaluates the entire X chromosome for copy number variations (deletions and duplications) at a high resolution.	Peripheral Whole Blood	25 working days	3,600.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Copy Number Variations (CNVs)", "Single Nucleotide Polymorphisms (SNPs) on X chromosome"] Parameters [] Preparation ["No special preparation is required"] Indications ["Suspected X-linked intellectual disability", "Diagnosis of developmental delay", "Investigation of congenital anomalies", "Prenatal screening (if indicated)"] Measurement technique Confirm with laboratory Codes LOINC: 82121-3 ICD-10: Q99.8, Q97.8, Q98.8 Clinical summary This test evaluates the entire X chromosome for copy number variations (deletions and duplications) at a high resolution.
TEST-1722 Chromosomes 18, X & Y (FISH) Test This diagnostic test evaluates fetal chromosomes 18, X, and Y using FISH to detect common aneuploidies like trisomy 18, Turner syndrome, and Klinefelter syndrome.	Amniotic Fluid or Chorionic Villus	3–4 Days	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosome 18 copy number", "Sex chromosome (X and Y) copy number"] Parameters [] Preparation [] Indications ["Prenatal screening for trisomy 18", "Prenatal screening for Turner syndrome (45,X)", "Prenatal screening for Klinefelter syndrome (47,XXY)", "Rapid assessment of fetal aneuploidy risk"] Measurement technique Confirm with laboratory Codes LOINC: 82159-9 ICD-10: Z36.2 Clinical summary This diagnostic test evaluates fetal chromosomes 18, X, and Y using FISH to detect common aneuploidies like trisomy 18, Turner syndrome, and Klinefelter syndrome.
TEST-646 ChromUltra Chromosome SNP HD Microarray Test This test evaluates the entire genome for copy number variations (CNVs), loss of heterozygosity (LOH), and single nucleotide polymorphisms (SNPs) to detect chromosomal abnormalitie...	Whole Blood (Peripheral)	15 Working Days	3,300.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Copy Number Variations (CNVs)", "Loss of Heterozygosity (LOH)", "Single Nucleotide Polymorphisms (SNPs)", "Chromosomal microdeletions", "Chromosomal duplications", "Regions of homozygosity"] Parameters [] Preparation ["Fasting is not required", "Ensure mandatory Genomic Microarray Requisition Form 19 is completed", "Inform phlebotomy team of all current medications, especially anticoagulants or antiplatelet agents"] Indications ["Evaluation of developmental delay or intellectual disability", "Investigation of multiple congenital anomalies", "Diagnosis of autism spectrum disorders", "Assessment of unexplained recurrent miscarriages", "Prenatal screening for chromosomal abnormalities"] Measurement technique Confirm with laboratory Codes LOINC: 92818-1 ICD-10: Z13.79 Clinical summary This test evaluates the entire genome for copy number variations (CNVs), loss of heterozygosity (LOH), and single nucleotide polymorphisms (SNPs) to detect chromosomal abnormalities.
TEST-1694 Cord Blood Karyotyping Test This test analyzes fetal chromosomes from umbilical cord blood to identify numerical and structural abnormalities.	Cord Blood (whole blood)	7–9 working days	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal number", "Chromosomal structure"] Parameters [] Preparation [] Indications ["Prenatal screening for chromosomal abnormalities", "Detection of Down syndrome", "Detection of Turner syndrome", "Detection of structural rearrangements"] Measurement technique Confirm with laboratory Codes LOINC: 20775-0 ICD-10: Z36.8 Clinical summary This test analyzes fetal chromosomes from umbilical cord blood to identify numerical and structural abnormalities.
TEST-628 Couple Chromosome Karyotype Analysis (Blood) Test This diagnostic test evaluates the number and structure of chromosomes in both partners' blood cells.	Peripheral whole blood (EDTA or heparin)	10–12 working days	2,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal structure", "Number of chromosomes"] Parameters [] Preparation ["Inform phlebotomist of all current prescriptions", "Do not discontinue prescribed medication without consulting physician"] Indications ["Infertility investigation", "Recurrent pregnancy loss", "Investigation of hereditary disorders"] Measurement technique Confirm with laboratory Codes LOINC: 34556-5 ICD-10: Z31.81, Z31.5, Z31.41 Clinical summary This diagnostic test evaluates the number and structure of chromosomes in both partners' blood cells.
TEST-1690 CRLF2 Gene Rearrangement (CML, AML, ALL) FISH Test This test detects structural rearrangements of the CRLF2 gene, which are associated with certain types of leukemia.	Peripheral Blood or Bone Marrow	3–4 Business Days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CRLF2 gene rearrangements", "Structural abnormalities in chromosomes X and Y"] Parameters [] Preparation ["No specific patient preparation required", "Requires a valid doctor’s prescription"] Indications ["Diagnosis and classification of ALL, CML, AML", "Risk stratification in leukemia", "Guidance for targeted therapy selection"] Measurement technique Confirm with laboratory Codes LOINC: 69247-7 ICD-10: C91.00, C92.00, C92.10 Clinical summary This test detects structural rearrangements of the CRLF2 gene, which are associated with certain types of leukemia.
TEST-1661 Del(20q) (MDS) FISH Test This diagnostic test evaluates for the presence of a deletion on the long arm of chromosome 20 (Del(20q)) using Fluorescence In-Situ Hybridization (FISH) technology.	Bone Marrow / Peripheral Blood	3–4 Days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Deletion of chromosome 20q", "Cytogenetic abnormality"] Parameters [] Preparation ["Doctor’s prescription is mandatory", "No fasting required unless instructed otherwise"] Indications ["Diagnosis and prognosis of Myelodysplastic Syndromes (MDS)", "Risk stratification in MDS"] Measurement technique Confirm with laboratory Codes LOINC: 38070-1 ICD-10: D46.7 Clinical summary This diagnostic test evaluates for the presence of a deletion on the long arm of chromosome 20 (Del(20q)) using Fluorescence In-Situ Hybridization (FISH) technology.
TEST-1663 Del(5q) (MDS) FISH Test This diagnostic test evaluates for the presence of a deletion on the long arm of chromosome 5 (del(5q)) in bone marrow or peripheral blood cells.	Bone Marrow / Peripheral Blood	3–4 Days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Deletion of the long arm of chromosome 5 (5q deletion)"] Parameters [] Preparation ["No dietary or medication preparation is typically required", "Must present a valid physician’s prescription"] Indications ["Diagnosis of Myelodysplastic Syndrome (MDS)", "Prognostic risk stratification in MDS", "Guiding lenalidomide therapy"] Measurement technique Confirm with laboratory Codes LOINC: 69002-3 ICD-10: D46.0, D46.9, Z15.81 Clinical summary This diagnostic test evaluates for the presence of a deletion on the long arm of chromosome 5 (del(5q)) in bone marrow or peripheral blood cells.
TEST-1657 Deletion 7q (MDS) Test This diagnostic test evaluates for the presence of interstitial deletions on the long arm of chromosome 7 (del(7q)) using Fluorescence In-Situ Hybridization (FISH).	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 ["Interstitial deletion of chromosome 7q", "Cytogenetic abnormality in bone marrow cells"] Parameters [] Preparation ["No fasting required for peripheral blood draw", "Follow physician's instructions for bone marrow aspiration, potentially withholding anticoagulants", "Continue all other medications unless advised otherwise by your doctor"] Indications ["Diagnosis and risk stratification of Myelodysplastic Syndromes (MDS)", "Guiding treatment decisions in MDS"] Measurement technique Confirm with laboratory Codes LOINC: 49596-9 ICD-10: D46.9 Clinical summary This diagnostic test evaluates for the presence of interstitial deletions on the long arm of chromosome 7 (del(7q)) using Fluorescence In-Situ Hybridization (FISH).
TEST-1169 EGFR Gene Amplification (FISH) Test This diagnostic test evaluates the number of copies of the EGFR gene within tumor cells using Fluorescence In-Situ Hybridization (FISH). It identifies gene amplification, a key bio...	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 ["EGFR gene copy number", "Gene amplification"] Parameters [] Preparation ["No patient preparation required", "FFPE tissue block submission with completed Form 17"] Indications ["Non-small cell lung cancer", "Colorectal carcinoma", "Glioblastoma", "Targeted therapy selection"] Measurement technique Confirm with laboratory Codes LOINC: 21674-1 ICD-10: Z13.89 Clinical summary This diagnostic test evaluates the number of copies of the EGFR gene within tumor cells using Fluorescence In-Situ Hybridization (FISH). It identifies gene amplification, a key biomarker for targeted cancer therapy.
TEST-2422 Expert Breast Cancer Panel Test This diagnostic test evaluates key biomarkers on breast tumour tissue to determine its subtype and guide personalised treatment.	Formalin-fixed paraffin-embedded (FFPE) tissue block, unstained slides, or cytology smears	10 working days from sample receipt	1,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Oestrogen Receptor (ER)", "Progesterone Receptor (PR)", "HER2/neu protein", "Ki-67 proliferation index", "Reflex markers"] Parameters [{"name": "ER (Oestrogen Receptor)", "reference_range": null}, {"name": "PR (Progesterone Receptor)", "reference_range": null}, {"name": "HER2/neu protein", "reference_range": null}, {"name": "Ki-67 proliferation index", "reference_range": null}] Preparation [] Indications ["Diagnosis of breast malignancy", "Guidance for personalised breast cancer therapy", "Assessment of treatment response"] Measurement technique Confirm with laboratory Codes LOINC: 95941-3 ICD-10: C50.919, Z85.3, Z15.01 Clinical summary This diagnostic test evaluates key biomarkers on breast tumour tissue to determine its subtype and guide personalised treatment.
TEST-1599 Fetal Blood for Karyotyping Test This test evaluates the number and structure of chromosomes in fetal blood cells to detect abnormalities.	Fetal whole blood (cordocentesis)	7–9 Working Days	600.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal number (aneuploidy)", "Chromosomal structure (translocations, deletions, duplications)"] Parameters [] Preparation ["No specific fasting required.", "Inform your doctor about all medications and supplements."] Indications ["Abnormal prenatal screening results", "Advanced maternal age", "Family history of chromosomal abnormalities", "Abnormal ultrasound findings"] Measurement technique Confirm with laboratory Codes LOINC: 34575-2 ICD-10: Z36.0 Clinical summary This test evaluates the number and structure of chromosomes in fetal blood cells to detect abnormalities.
TEST-1178 FGFR1 (8p12) Gene Rearrangement (FISH) Test This test detects rearrangements in the FGFR1 gene located on chromosome 8p12 using fluorescence in-situ hybridization (FISH). It is used to aid in the diagnosis and treatment plan...	Peripheral Blood (whole blood, EDTA) or Bone Marrow Aspirate	4 working days	850.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["FGFR1 gene rearrangement", "Split signal pattern in interphase nuclei"] Parameters [] Preparation ["No fasting required for peripheral blood collection", "Follow haematologist’s instructions for bone marrow aspiration"] Indications ["Suspected myeloid/lymphoid neoplasms with eosinophilia (M/LN-eo)", "Guidance for targeted therapy selection"] Measurement technique Confirm with laboratory Codes LOINC: 92888-9 ICD-10: D47.5 Clinical summary This test detects rearrangements in the FGFR1 gene located on chromosome 8p12 using fluorescence in-situ hybridization (FISH). It is used to aid in the diagnosis and treatment planning for specific hematological malignancies.
TEST-1604 FGFR1 Gene Rearrangement FISH Test This diagnostic test evaluates for chromosomal rearrangements involving the FGFR1 gene, often associated with specific types of leukemia and myeloproliferative neoplasms.	Bone Marrow Aspirate	3–4 business days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["FGFR1 gene rearrangements", "Chromosomal translocations (8p11 syndrome)"] Parameters [] Preparation ["No fasting required", "Do not discontinue prescribed medication without doctor approval"] Indications ["Diagnosis of myeloid/lymphoid neoplasms", "Selection of tyrosine kinase inhibitor therapy", "Monitoring disease progression"] Measurement technique Confirm with laboratory Codes LOINC: 98172-3 ICD-10: C94.8 Clinical summary This diagnostic test evaluates for chromosomal rearrangements involving the FGFR1 gene, often associated with specific types of leukemia and myeloproliferative neoplasms.

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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