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 46–51 of 51 matching tests.

FISH diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-1203 Prader-Willi Syndrome (FISH) Genetic Testing Test This test detects the presence or absence of a microdeletion in the 15q11-q13 region of chromosome 15, the most common cause of Prader-Willi syndrome.	Peripheral Blood (EDTA), Amniotic Fluid, Chorionic Villi, Cord Blood	3-4 business days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosome 15q11-q13 deletion"] Parameters [] Preparation [] Indications ["Suspected Prader-Willi syndrome", "Neonatal hypotonia", "Feeding difficulties", "Characteristic facial features", "Hyperphagia"] Measurement technique Confirm with laboratory Codes LOINC: 26462-5 ICD-10: Q87.1 Clinical summary This test detects the presence or absence of a microdeletion in the 15q11-q13 region of chromosome 15, the most common cause of Prader-Willi syndrome.
TEST-1208 Prader‑Willi Syndrome FISH Test (SNRPN Locus) This diagnostic test evaluates for the presence of a microdeletion in the SNRPN locus on chromosome 15q11-q13, a key genetic marker for Prader-Willi syndrome.	Whole blood	4 working days	1,500.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SNRPN locus deletion", "Chromosome 15q11-q13 region"] Parameters [] Preparation ["No specific fasting required", "Avoid recent blood transfusion (< 2 weeks)"] Indications ["Clinical suspicion of Prader-Willi syndrome", "Evaluation of developmental delay", "Assessment of hypotonia in infancy"] Measurement technique Confirm with laboratory Codes LOINC: 34441-1 ICD-10: Q87.1 Clinical summary This diagnostic test evaluates for the presence of a microdeletion in the SNRPN locus on chromosome 15q11-q13, a key genetic marker for Prader-Willi syndrome.
TEST-478 Semen FISH Analysis Test This diagnostic test evaluates the chromosomal integrity of spermatozoa, detecting numerical and structural abnormalities.	Semen (fresh ejaculate)	10–12 working days	1,000.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosomal aneuploidies", "Y-chromosome microdeletions (AZF regions)", "Structural rearrangements (translocations)"] Parameters [] Preparation ["Sexual abstinence of 2–5 days", "Avoid alcohol for 48 hours", "Collect entire ejaculate into sterile container"] Indications ["Idiopathic male infertility", "Investigation of recurrent pregnancy loss", "Pre-implantation genetic testing (PGT) planning"] Measurement technique Confirm with laboratory Codes LOINC: 33763-8 ICD-10: N46.9 Clinical summary This diagnostic test evaluates the chromosomal integrity of spermatozoa, detecting numerical and structural abnormalities.
TEST-1096 Synovial Sarcoma SS18 FISH (Fluorescence In-Situ Hybridization) Test This diagnostic test evaluates for the presence of the SS18 gene rearrangement, a specific chromosomal translocation associated with synovial sarcoma.	Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Block or Fresh Tumor Tissue	7–8 working days	1,200.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SS18 gene rearrangement", "t(X;18)(p11.2;q11.2) translocation"] Parameters [] Preparation [] Indications ["Confirmation of synovial sarcoma diagnosis", "Evaluation of equivocal immunohistochemistry results", "Guiding treatment decisions"] Measurement technique Confirm with laboratory Codes LOINC: 77637-2 ICD-10: C49.9, Z15.09, Z80.8 Clinical summary This diagnostic test evaluates for the presence of the SS18 gene rearrangement, a specific chromosomal translocation associated with synovial sarcoma.
TEST-1073 Trisomy 12 (CLL) FISH Test This diagnostic test evaluates for the presence of an extra copy of chromosome 12 in blood or bone marrow cells, a significant prognostic marker in Chronic Lymphocytic Leukemia (CL...	Bone marrow aspirate or peripheral blood	3–4 working days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Chromosome 12 copy number", "Presence of +12 abnormality"] Parameters [] Preparation [] Indications ["Diagnosis and prognosis of Chronic Lymphocytic Leukemia (CLL)", "Risk stratification in CLL patients"] Measurement technique Confirm with laboratory Codes LOINC: 60508-8 ICD-10: C91.1 Clinical summary This diagnostic test evaluates for the presence of an extra copy of chromosome 12 in blood or bone marrow cells, a significant prognostic marker in Chronic Lymphocytic Leukemia (CLL).
TEST-1056 Williams Syndrome (FISH) Test This test detects the 7q11.23 microdeletion associated with Williams syndrome using Fluorescence In Situ Hybridization (FISH).	Peripheral whole blood (EDTA tube)	3–4 days	700.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["7q11.23 microdeletion", "Elastin gene locus deletion"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any bleeding disorders or recent transfusions"] Indications ["Suspected Williams syndrome based on clinical presentation", "Confirmation of diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 69466-9 ICD-10: Q93.89 Clinical summary This test detects the 7q11.23 microdeletion associated with Williams syndrome using Fluorescence In Situ Hybridization (FISH).

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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Use the test details as a conversation starter

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.