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 31–45 of 51 matching tests.

FISH diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
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-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-1144 IGH Gene Break Apart (14q32.3) FISH Test This test detects rearrangements within the IGH gene located on chromosome 14q32.3 using Fluorescence In-Situ Hybridization (FISH). It is used for the diagnosis and prognosis of B-...	Peripheral Blood (Green-top Sodium Heparin Tube) or Bone Marrow Aspirate	4 working days	850.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["IGH gene rearrangements", "Translocations involving 14q32.3"] Parameters [] Preparation ["No fasting required for blood collection", "Completed Chromosome & FISH Requisition Form 17 is mandatory"] Indications ["Diagnosis of B-cell leukemias and lymphomas", "Prognosis and risk stratification in hematologic malignancies", "Guiding targeted therapy"] Measurement technique Confirm with laboratory Codes LOINC: 60528-5 ICD-10: C91.9, C92.9, C90.0 Clinical summary This test detects rearrangements within the IGH gene located on chromosome 14q32.3 using Fluorescence In-Situ Hybridization (FISH). It is used for the diagnosis and prognosis of B-cell leukemias and lymphomas.
TEST-1465 IRF4/MUM1 (IRFA‑MUM1) FISH Test This diagnostic test evaluates for rearrangements in the IRF4 gene using Fluorescence In-Situ Hybridization (FISH). It is crucial for diagnosing and monitoring specific haematologi...	Archival Solid Tissue (FFPE Block or Slides)	7–8 business days	1,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["IRF4 gene rearrangement", "Fluorescence In-Situ Hybridization (FISH) signal patterns"] Parameters [] Preparation ["No fasting required", "No medication changes required", "Bring valid DHA-doctor’s prescription", "Bring formalin-fixed paraffin-embedded tissue block or slides"] Indications ["Diagnosis of plasma cell myeloma", "Diagnosis of specific large B-cell lymphomas", "Prognosis assessment", "Minimal residual disease monitoring"] Measurement technique Confirm with laboratory Codes LOINC: 88213-0 ICD-10: C90.00 Clinical summary This diagnostic test evaluates for rearrangements in the IRF4 gene using Fluorescence In-Situ Hybridization (FISH). It is crucial for diagnosing and monitoring specific haematological malignancies.
TEST-1408 MAF/IGH FISH Test (Multiple Myeloma Translocation) This diagnostic test evaluates for the presence of the t(14;16) translocation, a specific genetic rearrangement linked to high-risk multiple myeloma.	Bone Marrow Aspirate (Primary) / Peripheral Blood (Alternative)	3–4 business days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["t(14;16) translocation", "IGH/MAF gene fusion"] Parameters [] Preparation [] Indications ["Diagnosis of multiple myeloma", "Risk stratification in plasma cell disorders", "Treatment planning"] Measurement technique Confirm with laboratory Codes LOINC: 49498-9 ICD-10: C90.0 Clinical summary This diagnostic test evaluates for the presence of the t(14;16) translocation, a specific genetic rearrangement linked to high-risk multiple myeloma.
TEST-1195 MYCN Amplification (FISH) Test This diagnostic test evaluates the presence and degree of MYCN gene amplification in tumor tissue using Fluorescence In-Situ Hybridization (FISH).	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 ["MYCN gene copy number", "Gene amplification status"] Parameters [] Preparation ["No patient preparation is needed"] Indications ["Risk stratification in neuroblastoma", "Guiding therapy decisions in neuroblastoma"] Measurement technique Confirm with laboratory Codes LOINC: 41644-0 ICD-10: C74.9 Clinical summary This diagnostic test evaluates the presence and degree of MYCN gene amplification in tumor tissue using Fluorescence In-Situ Hybridization (FISH).
TEST-1200 NTRK1 Gene Rearrangement Assay (FISH) Test This diagnostic test evaluates for specific genomic rearrangements of the NTRK1 gene in solid tumor tissue.	Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Block or Slides (Archival Tissue Specimen)	4 working days	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["NTRK1 gene rearrangements", "Presence of specific fusions"] Parameters [] Preparation ["No special preparation required", "Ensure Genomics Clinical Information Requisition Form (Form 20) is completed"] Indications ["Solid tumors", "Eligibility assessment for TRK inhibitor therapy"] Measurement technique Confirm with laboratory Codes LOINC: 92896-2 ICD-10: Z15.09 Clinical summary This diagnostic test evaluates for specific genomic rearrangements of the NTRK1 gene in solid tumor tissue.
TEST-1207 NTRK3 Gene Rearrangement FISH Assay Test This diagnostic test evaluates for the presence of NTRK3 gene rearrangements (fusions) within solid tumor tissue samples.	Archival Tissue Specimen (FFPE block or slides)	4 Working Days	800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["NTRK3 gene fusions", "Presence of specific genetic alterations"] Parameters [] Preparation ["Submit FFPE tissue block or slides", "Ensure Genomics Clinical Information Requisition Form (Form 20) is completed"] Indications ["Identification of NTRK3 gene fusions in solid tumors", "Guiding targeted therapy with TRK inhibitors", "Diagnosis of NTRK fusion-positive cancers"] Measurement technique Confirm with laboratory Codes LOINC: 92831-1 ICD-10: C49.9 Clinical summary This diagnostic test evaluates for the presence of NTRK3 gene rearrangements (fusions) within solid tumor tissue samples.
TEST-1226 PML/RARA Fusion Gene FISH Test (t(15;17)) This diagnostic test evaluates for the presence of the PML/RARA fusion gene, the defining molecular hallmark of Acute Promyelocytic Leukemia (APL).	Peripheral Whole Blood or Bone Marrow Aspirate	4 working days	750.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PML/RARA fusion gene", "t(15;17) translocation"] Parameters [] Preparation [] Indications ["Suspected Acute Promyelocytic Leukemia (APL)", "Rapid genetic confirmation of t(15;17) translocation"] Measurement technique Confirm with laboratory Codes LOINC: 60511-1 ICD-10: C92.4 Clinical summary This diagnostic test evaluates for the presence of the PML/RARA fusion gene, the defining molecular hallmark of Acute Promyelocytic Leukemia (APL).

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.