Gene Sequencing tests in Dubai & UAE

Compare available Gene Sequencing 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

143

Listed price range

2,600.00–3,200.00 AED

Clinical preparation

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Gene Sequencing test prices

Showing 136–143 of 143 matching tests.

Gene Sequencing diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3658 TRMU Gene Transient Infantile Liver Failure Genetic Test This test detects pathogenic variants in the TRMU gene associated with transient infantile liver failure using next-generation sequencing.	Whole blood (EDTA) or FTA card blood spot	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the TRMU gene", "Full coding region, splice sites, and flanking intronic regions"] Parameters [] Preparation ["No fasting required", "No specific medication or diet instructions"] Indications ["Infants presenting with acute, reversible liver failure", "Family history suggestive of TRMU-related liver disease"] Measurement technique Confirm with laboratory Codes LOINC: 94219-0 ICD-10: K72.90 Clinical summary This test detects pathogenic variants in the TRMU gene associated with transient infantile liver failure using next-generation sequencing.
TEST-4648 USB1 Gene Poikiloderma with Neutropenia (Clericuzio Type) Genetic Test This genetic test analyzes the USB1 gene to identify pathogenic variants associated with Clericuzio-type poikiloderma with neutropenia.	3 mL peripheral whole blood in EDTA (purple-top) tube	3–4 weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["USB1 gene coding regions", "USB1 gene splice junctions"] Parameters [] Preparation [] Indications ["Suspected Clericuzio-type poikiloderma with neutropenia", "Family history of the disorder"] Measurement technique Confirm with laboratory Codes LOINC: 81272-4 ICD-10: Q82.8 Clinical summary This genetic test analyzes the USB1 gene to identify pathogenic variants associated with Clericuzio-type poikiloderma with neutropenia.
TEST-6247 VARS2 Gene Combined Oxidative Phosphorylation Deficiency Type 20 Genetic Test This test identifies pathogenic variants in the VARS2 gene, which are associated with combined oxidative phosphorylation deficiency type 20.	Whole Blood (EDTA)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the VARS2 gene", "Copy Number Variants (CNVs) in VARS2"] Parameters [] Preparation [] Indications ["Suspected combined oxidative phosphorylation deficiency type 20 (COXPD20)", "Infantile onset encephalopathy with seizures and lactic acidosis"] Measurement technique Confirm with laboratory Codes LOINC: 95209-3 ICD-10: E88.49 Clinical summary This test identifies pathogenic variants in the VARS2 gene, which are associated with combined oxidative phosphorylation deficiency type 20.
TEST-4372 VDAC1 Gene Mitochondrial Encephalopathy Genetic Test This test identifies pathogenic variants in the VDAC1 gene, which are associated with mitochondrial encephalopathy.	Whole Blood (EDTA tube, 3–5 mL) or Dried Blood Spot (FTA card)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the VDAC1 gene", "Single nucleotide variants", "Small insertions or deletions"] Parameters [] Preparation ["A genetic counselling session is required.", "Provide a detailed clinical history including neurological symptom onset, seizure semiology, and prior biochemical or imaging results.", "Document a three-generation pedigree.", "Obtain informed consent."] Indications ["Patients with unexplained neurological regression", "Patients with treatment-resistant seizures", "Patients with multisystem mitochondrial symptoms", "At-risk family members undergoing cascade screening"] Measurement technique Confirm with laboratory Codes LOINC: 93306-2 ICD-10: G31.81 Clinical summary This test identifies pathogenic variants in the VDAC1 gene, which are associated with mitochondrial encephalopathy.
TEST-4049 VPS13A Gene Choreoacanthocytosis Genetic Test This genetic test evaluates the VPS13A gene for mutations associated with choreoacanthocytosis.	Whole blood (3–5 mL in EDTA) or extracted DNA	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["VPS13A gene variants", "Single Nucleotide Variants (SNVs)", "Insertions/Deletions (indels)"] Parameters [] Preparation ["No specific preparation required"] Indications ["Suspected choreoacanthocytosis", "Family history of choreoacanthocytosis", "Diagnostic confirmation"] Measurement technique Confirm with laboratory Codes LOINC: 48834-2 ICD-10: G24.5 Clinical summary This genetic test evaluates the VPS13A gene for mutations associated with choreoacanthocytosis.
TEST-3402 WDR11 Gene Hypogonadotropic Hypogonadism Type 14 Genetic Test This genetic test identifies mutations in the WDR11 gene associated with hypogonadotropic hypogonadism type 14.	Peripheral whole blood or buccal swab	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic and likely pathogenic variants in the WDR11 gene"] Parameters [] Preparation ["No specific fasting required", "Inform phlebotomist of any medications"] Indications ["Diagnosis of hypogonadotropic hypogonadism type 14", "Genetic counselling for affected individuals and families", "Guiding fertility treatments and hormone replacement therapy"] Measurement technique Confirm with laboratory Codes LOINC: 81222-9 ICD-10: E23.0 Clinical summary This genetic test identifies mutations in the WDR11 gene associated with hypogonadotropic hypogonadism type 14.
TEST-2297 WDR60 Gene Short‑Rib Thoracic Dysplasia Type 8 with or without Polydactyly Genetic Test This genetic test identifies pathogenic variants in the WDR60 gene associated with Short‑Rib Thoracic Dysplasia type 8 (SRTD8).	Whole Blood, Extracted DNA, Dried Blood Spot (FTA Card)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the WDR60 gene", "Large deletions and duplications in the WDR60 gene"] Parameters [] Preparation ["Genetic counselling session mandatory before sample collection", "No specific fasting or medication restrictions mentioned"] Indications ["Newborns, infants, and children with clinical features suggestive of SRTD8", "Families with a history of SRTD8", "Unexplained neonatal deaths due to skeletal dysplasia", "Prenatal testing after prior genetic confirmation in the family"] Measurement technique Confirm with laboratory Codes LOINC: 59409-2 ICD-10: Q77.2 Clinical summary This genetic test identifies pathogenic variants in the WDR60 gene associated with Short‑Rib Thoracic Dysplasia type 8 (SRTD8).
TEST-3534 WFS1 Gene (Cataract Type 41) Genetic Test This test evaluates the WFS1 gene for pathogenic variants associated with autosomal recessive cataracts type 41 and Wolfram syndrome.	Whole blood (EDTA tube) or FTA card (dried blood spot)	3–4 Weeks (expedited 2-week option available)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Single nucleotide variants (SNVs)", "Small insertions/deletions (indels)", "Copy number variations (CNVs)", "WFS1 gene sequence"] Parameters [] Preparation ["No fasting required", "No medication changes required", "Mandatory pre-test genetic counselling session"] Indications ["Diagnosis of congenital/early-onset cataracts", "Diagnosis of Wolfram syndrome (DIDMOAD)", "Genetic counselling for families with a history of these conditions", "Carrier screening in at-risk individuals"] Measurement technique Confirm with laboratory Codes LOINC: 21662-0 ICD-10: Q12.0 Clinical summary This test evaluates the WFS1 gene for pathogenic variants associated with autosomal recessive cataracts type 41 and Wolfram syndrome.

Category overview

Gene Sequencing: overview

Achieving a definitive diagnosis for a complex or rare genetic disorder often requires reading the entire genetic code of specific genes to find elusive, hidden errors. As a cornerstone of our advanced Genetics services, Gene Sequencing expansively scans the targeted regions of your genome to uncover rare or novel mutations that standard tests miss. Utilizing state-of-the-art sequencing technology, this comprehensive molecular profiling delivers the critical data necessary to safely guide your healthcare provider in tailoring highly personalized medical management and targeted therapeutic interventions. Trusted for molecular excellence among premier diagnostic labs in the UAE, DNA Labs ensures absolute patient confidentiality, exceptional analytical precision, and remarkably fast reporting. Find the clear, definitive answers you need—schedule your gene sequencing testing in UAE, coordinate a seamless clinical sample transfer, or consult our expert medical genetics professionals 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.