Genetic Sequencing tests in Dubai & UAE

Compare available Genetic 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

256

Listed price range

2,600.00–5,000.00 AED

Clinical preparation

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Genetic Sequencing test prices

Showing 61–75 of 256 matching tests.

Genetic Sequencing diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-3731 CR2 Gene Common Variable Immunodeficiency Type 7 (CVID7) Genetic Test This test evaluates the CR2 gene for pathogenic variants associated with Common Variable Immunodeficiency Type 7 (CVID7).	Peripheral whole blood (EDTA) 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 variants in the CR2 gene", "Single nucleotide variants (SNVs)", "Insertions and deletions (Indels)", "Copy number variations (CNVs)", "Large rearrangements"] Parameters [] Preparation [] Indications ["Suspected Common Variable Immunodeficiency Type 7 (CVID7)", "Recurrent respiratory or gastrointestinal infections", "Poor vaccine responses", "Unexplained low immunoglobulins", "Family history of primary immunodeficiency"] Measurement technique Confirm with laboratory Codes LOINC: 94288-6 ICD-10: D80.1 Clinical summary This test evaluates the CR2 gene for pathogenic variants associated with Common Variable Immunodeficiency Type 7 (CVID7).
TEST-4737 CREB3L1 Genetic Test for Osteogenesis Disorders This test evaluates the entire coding region of the CREB3L1 gene for pathogenic variants associated with osteogenesis imperfecta and related connective tissue disorders.	Whole Blood or FTA Card	21–28 days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CREB3L1 gene sequence", "Copy number variations (CNV) in CREB3L1"] Parameters [] Preparation ["No fasting required", "Pre-test genetic counselling session is mandatory"] Indications ["Clinical signs of brittle bone disease", "Family history of Osteogenesis Imperfecta (OI)", "Prenatal diagnosis when a familial mutation is known"] Measurement technique Confirm with laboratory Codes LOINC: 92813-1 ICD-10: Q78.0 Clinical summary This test evaluates the entire coding region of the CREB3L1 gene for pathogenic variants associated with osteogenesis imperfecta and related connective tissue disorders.
TEST-3545 CTC1 Gene Sequencing (Coat Plus Syndrome) Genetic Test This test evaluates the CTC1 gene for pathogenic variants associated with Coat Plus syndrome (CRMCC) and related telomere biology disorders.	Whole Blood (EDTA), FTA card, or Extracted DNA	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 CTC1 gene", "Telomere biology disorder risk"] Parameters [] Preparation ["No fasting required", "Provide detailed clinical history", "Attend a 30-minute genetic counselling session"] Indications ["Diagnosis of Coat Plus syndrome (CRMCC)", "Diagnosis of related telomere biology disorders", "Genetic counseling for families with suspected CRMCC"] Measurement technique Confirm with laboratory Codes LOINC: 81407-5 ICD-10: Q87.8 Clinical summary This test evaluates the CTC1 gene for pathogenic variants associated with Coat Plus syndrome (CRMCC) and related telomere biology disorders.
TEST-6139 CYP11B2 Genetic Test for Congenital Hypoaldosteronism (CMO I Deficiency) This test evaluates the CYP11B2 gene for pathogenic variants associated with Congenital Hypoaldosteronism Type I (CMO I deficiency). It identifies mutations causing a rare, life-th...	Peripheral Venous Whole Blood (EDTA) or 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 CYP11B2 gene", "Presence of mutations causing CMO I deficiency"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any medications"] Indications ["Infants presenting with symptoms suggestive of salt-wasting crisis", "Family history of CMO I deficiency", "Confirmation of diagnosis after biochemical screening", "Carrier testing for family members", "Prenatal counselling"] Measurement technique Confirm with laboratory Codes LOINC: 21621-4 ICD-10: E27.4 Clinical summary This test evaluates the CYP11B2 gene for pathogenic variants associated with Congenital Hypoaldosteronism Type I (CMO I deficiency). It identifies mutations causing a rare, life-threatening salt-wasting disorder.
TEST-3985 CYP27A1 Genetic Sequencing Test for Cerebrotendinous Xanthomatosis This test identifies pathogenic variants in the CYP27A1 gene associated with Cerebrotendinous Xanthomatosis (CTX).	Whole blood (EDTA tube), extracted DNA, or 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 CYP27A1 gene", "Copy number variations in CYP27A1 gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab of current medications"] Indications ["Suspected Cerebrotendinous Xanthomatosis (CTX)", "Family history of CTX", "Progressive neurological symptoms suggestive of CTX"] Measurement technique Confirm with laboratory Codes LOINC: 48808-7 ICD-10: E75.5 Clinical summary This test identifies pathogenic variants in the CYP27A1 gene associated with Cerebrotendinous Xanthomatosis (CTX).
TEST-4971 CYP4F22 Gene Ichthyosis, Lamellar Type 3 Genetic Test This genetic test identifies pathogenic variants in the CYP4F22 gene associated with autosomal recessive lamellar ichthyosis type 3.	Peripheral Blood (EDTA) 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 variants in CYP4F22 gene coding regions", "Pathogenic variants in CYP4F22 gene splice sites"] Parameters [] Preparation ["Pre-genetic counselling session required", "Inform phlebotomist of anticoagulant use", "No fasting required"] Indications ["Suspected lamellar ichthyosis type 3", "Family history of lamellar ichthyosis type 3", "Genetic counselling for affected families"] Measurement technique Confirm with laboratory Codes LOINC: 92185-1 ICD-10: Q80.2 Clinical summary This genetic test identifies pathogenic variants in the CYP4F22 gene associated with autosomal recessive lamellar ichthyosis type 3.
TEST-4562 DCLRE1C Gene Test This genetic test evaluates the DCLRE1C gene for mutations associated with Severe Combined Immunodeficiency (Athabascan type). It detects various genetic alterations including sing...	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 ["DCLRE1C gene sequence", "Copy Number Variants (CNV) in DCLRE1C", "Single Nucleotide Variants (SNV)", "Insertions/Deletions (Indels)"] Parameters [] Preparation ["No special preparation required."] Indications ["Clinical suspicion of Severe Combined Immunodeficiency (Athabascan type)", "Family history of SCID", "Carrier screening for family planning"] Measurement technique Confirm with laboratory Codes LOINC: 21665-0 ICD-10: D81.2 Clinical summary This genetic test evaluates the DCLRE1C gene for mutations associated with Severe Combined Immunodeficiency (Athabascan type). It detects various genetic alterations including single nucleotide variants, insertions/deletions, and copy number variants.
TEST-5086 DGUOK Gene Mitochondrial DNA Depletion Syndrome Genetic Test This genetic test detects mutations in the DGUOK gene associated with mitochondrial DNA depletion syndrome.	Whole blood (K2-EDTA tube, 2 mL) or FTA card (dried blood spots)	3–4 weeks from receipt of sample	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DGUOK gene mutations", "Single nucleotide variants", "Small insertions and deletions", "Copy number variations"] Parameters [] Preparation [] Indications ["Infants, children, and adults presenting with elevated liver transaminases, neurological regression, hypotonia, or lactic acidosis where mitochondrial hepatopathy or encephalomyopathy is suspected.", "Asymptomatic siblings and relatives for carrier screening following identification of a confirmed familial mutation."] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: E88.49 Clinical summary This genetic test detects mutations in the DGUOK gene associated with mitochondrial DNA depletion syndrome.
TEST-3092 DLL4 Gene Adams-Oliver Syndrome Type 6 Genetic Test This genetic test evaluates the DLL4 gene for pathogenic variants associated with Adams-Oliver syndrome type 6.	Peripheral whole blood (3–5 mL in EDTA) or extracted gDNA	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 DLL4 gene"] Parameters [] Preparation [] Indications ["Suspected Adams-Oliver syndrome type 6", "Familial risk assessment for DLL4-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q87.2 Clinical summary This genetic test evaluates the DLL4 gene for pathogenic variants associated with Adams-Oliver syndrome type 6.
TEST-4466 DPAGT1 Gene Congenital Disorder of Glycosylation Type 1J (CDG‑Ij) Genetic Test This test identifies mutations in the DPAGT1 gene, confirming a diagnosis of Congenital Disorder of Glycosylation Type 1J (CDG‑Ij).	Peripheral whole blood (EDTA or FTA card)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DPAGT1 gene sequence", "Coding region and splice junctions"] Parameters [] Preparation ["No specific fasting required", "Do not stop, alter, or initiate any prescribed therapy without physician consultation"] Indications ["Unexplained neurological regression in a child", "Suspected Congenital Disorder of Glycosylation Type 1J"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: E77.8 Clinical summary This test identifies mutations in the DPAGT1 gene, confirming a diagnosis of Congenital Disorder of Glycosylation Type 1J (CDG‑Ij).
TEST-4995 DSC3 Gene Hypotrichosis and Recurrent Skin Vesicles Genetic Test This genetic test sequences the entire DSC3 gene to detect mutations associated with hypotrichosis and recurrent skin vesicles.	Peripheral Whole Blood, Buccal Swab, or FTA Card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DSC3 gene sequence", "Pathogenic mutations (SNVs, indels, CNVs)"] Parameters [] Preparation ["No special fasting required", "No medication changes required unless advised by physician"] Indications ["Suspected DSC3-related hypotrichosis", "Recurrent skin blistering", "Family history of related conditions"] Measurement technique Confirm with laboratory Codes LOINC: 80823-7 ICD-10: Q84.0 Clinical summary This genetic test sequences the entire DSC3 gene to detect mutations associated with hypotrichosis and recurrent skin vesicles.
TEST-4280 DSP Gene Cardiomyopathy, Dilated with Woolly Hair and Keratoderma Genetic Test This genetic test analyzes the DSP gene to detect pathogenic variants associated with DSP-related cardiomyopathy, woolly hair, and keratoderma.	Peripheral Whole Blood	3–4 Weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the DSP gene", "Single nucleotide variants", "Small insertions/deletions", "Large rearrangements"] Parameters [] Preparation ["Pre-test genetic counseling session is mandatory", "Do not discontinue prescribed medication without consulting physician"] Indications ["Clinical suspicion of DSP-related disorders", "Family history of DSP-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: I42.0, L85.2, Q84.1 Clinical summary This genetic test analyzes the DSP gene to detect pathogenic variants associated with DSP-related cardiomyopathy, woolly hair, and keratoderma.
TEST-3501 DUOX1 Gene Thyroid Dyshormonogenesis Type 6 Genetic Test This genetic test identifies pathogenic variants in the DUOX1 gene associated with thyroid dyshormonogenesis type 6.	Peripheral Blood (3 mL EDTA), Extracted DNA, or FTA Card	3 to 4 Weeks (express 14‑day option available)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["DUOX1 gene coding region variants", "Pathogenic mutations"] Parameters [] Preparation ["No fasting required", "No medication changes required"] Indications ["Diagnosis of thyroid dyshormonogenesis type 6", "Evaluation of congenital hypothyroidism", "Genetic counseling for families with affected individuals"] Measurement technique Confirm with laboratory Codes LOINC: 86234-4 ICD-10: E07.1, E03.1, Z13.29 Clinical summary This genetic test identifies pathogenic variants in the DUOX1 gene associated with thyroid dyshormonogenesis type 6.
TEST-2766 EDN3 Gene Hirschsprung Disease Genetic Test This test evaluates the endothelin-3 (EDN3) gene for pathogenic variants associated with Hirschsprung disease.	Peripheral whole blood (EDTA) or FTA card dried blood spot	3–4 Weeks (with interim verbal update)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the EDN3 gene", "Full gene coverage including exon-intron boundaries"] Parameters [] Preparation ["No special fasting required", "No medication adjustment required unless specified by referring physician"] Indications ["Newborns with intestinal obstruction", "Older children with chronic constipation", "Individuals with a family history of Hirschsprung disease"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q43.1 Clinical summary This test evaluates the endothelin-3 (EDN3) gene for pathogenic variants associated with Hirschsprung disease.
TEST-5949 EDNRB Gene Waardenburg Syndrome / Hirschsprung Disease Genetic Test This test analyzes the EDNRB gene to detect pathogenic variants associated with Waardenburg syndrome (sensorineural hearing loss, pigmentary anomalies) and Hirschsprung disease (co...	Peripheral Blood, Extracted DNA, or 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 EDNRB gene", "Missense, nonsense, splice-site, and small indel variants"] Parameters [] Preparation [] Indications ["Diagnosis of Waardenburg syndrome", "Diagnosis of Hirschsprung disease", "Genetic counselling for families with affected individuals", "Prenatal diagnosis in high-risk pregnancies"] Measurement technique Confirm with laboratory Codes LOINC: 82863-9 ICD-10: Q43.1, E70.3 Clinical summary This test analyzes the EDNRB gene to detect pathogenic variants associated with Waardenburg syndrome (sensorineural hearing loss, pigmentary anomalies) and Hirschsprung disease (congenital megacolon).

Category overview

Genetic Sequencing: overview

Achieving a definitive diagnosis for multi-system or exceptionally rare disorders requires reading the deepest layers of your foundational biological code. As the pinnacle of our advanced Genetics department, Genetic Sequencing (including Whole Exome or Whole Genome testing) provides an incredibly detailed, high-resolution scan of your DNA. By leveraging state-of-the-art Next-Generation Sequencing technology, this expansive molecular screening helps uncover elusive genetic variants that standard tests miss, safely guiding your healthcare provider in tailoring highly personalized medical treatments and opening doors to advanced precision medicine. Consistently trusted for advanced genomic analysis across premier diagnostic labs in Dubai and the UAE, DNA Labs ensures strict patient confidentiality, exceptional analytical precision, and highly efficient reporting. Secure the definitive insights your health requires—book your genetic sequencing testing in UAE, arrange a secure clinical sample collection, or consult our dedicated medical genetics experts.

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