Diagnostic options · UAE

FISH tests in Dubai & UAE

Compare available FISH 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

700.00–2,500.00 AED

Clinical preparation

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FISH test prices

Showing 1–15 of 51 matching tests.

FISH 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-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-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-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-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-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-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

FISH: overview

Navigating complex oncological or genetic challenges demands rapid, highly targeted insights to illuminate the best path forward for your health. Representing an advanced subspecialty within our Genetics services, FISH (Fluorescence In Situ Hybridization) testing maps specific genetic material within your cells using glowing probes. Utilizing this state-of-the-art diagnostic technology, our precise molecular screening helps detect subtle chromosomal abnormalities and tumor markers, offering the exact clarity needed to safely guide personalized therapeutic strategies. Consistently ranked among the best diagnostic labs in the UAE, DNA Labs ensures strict patient confidentiality, unparalleled analytical precision, and remarkably fast turnaround times for time-sensitive cases. Empower your customized medical care—schedule your FISH testing in UAE, book a seamless home sample collection, or consult our highly specialized genetics experts today.

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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.