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

Confirm test-specific instructions with your clinician or laboratory.

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Genetic Sequencing test prices

Showing 166–180 of 256 matching tests.

Genetic Sequencing diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4634 NDUFAF6 Gene Leigh Syndrome Genetic Test This genetic test evaluates the NDUFAF6 gene for variants associated with Leigh syndrome.	Peripheral whole blood (EDTA)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["NDUFAF6 gene sequence", "Pathogenic variants (SNVs, indels, large deletions/duplications)", "Mitochondrial complex I assembly factor function"] Parameters [] Preparation ["No specific fasting required", "No medication or diet restrictions"] Indications ["Clinical suspicion of Leigh syndrome", "Progressive neurological disorder of unknown etiology", "Family history of Leigh syndrome or related mitochondrial disorders"] Measurement technique Confirm with laboratory Codes LOINC: 21636-5 ICD-10: G31.81, E88.89, R94.0 Clinical summary This genetic test evaluates the NDUFAF6 gene for variants associated with Leigh syndrome.
TEST-5203 NOP10 Gene Dyskeratosis Congenita (Autosomal Recessive Type 1) NGS Test This test evaluates the NOP10 gene for pathogenic variants associated with autosomal recessive dyskeratosis congenita type 1.	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 NOP10 gene"] Parameters [] Preparation ["Submit clinical history", "Attend genetic counselling session", "Gather family medical records", "List current medications"] Indications ["Suspected dyskeratosis congenita", "Family history of dyskeratosis congenita", "Screening for cancer predisposition"] Measurement technique Confirm with laboratory Codes LOINC: 81321-0 ICD-10: D82.8 Clinical summary This test evaluates the NOP10 gene for pathogenic variants associated with autosomal recessive dyskeratosis congenita type 1.
TEST-4085 NOTCH1 Gene Aortic Valve Disease Type 1 Genetic Test This test identifies pathogenic variants in the NOTCH1 gene associated with Aortic Valve Disease type 1.	Peripheral Whole Blood (3–5 mL 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 NOTCH1 gene", "Full coding and splice-site coverage"] Parameters [] Preparation ["No specific fasting required", "Continue all prescribed medications unless instructed otherwise by physician"] Indications ["Personal or family history of bicuspid aortic valve", "Early-onset aortic stenosis or regurgitation", "Planning cardiac surgery", "First-degree relatives of confirmed NOTCH1 mutation carriers"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: I35.0, Q23.0 Clinical summary This test identifies pathogenic variants in the NOTCH1 gene associated with Aortic Valve Disease type 1.
TEST-5486 NPC1 Gene (Niemann‑Pick Type C1) Genetic Test This genetic test evaluates the NPC1 gene for pathogenic variants associated with Niemann-Pick disease type C1.	Peripheral Whole Blood (DNA extract)	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 NPC1 gene", "SNVs, indels, CNVs"] Parameters [] Preparation ["No fasting required", "No medication adjustments required", "Pre-test genetic counselling session required"] Indications ["Confirmation of suspected Niemann-Pick disease type C1", "Carrier screening in families with known mutations", "Prenatal or preimplantation genetic diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 81315-0 ICD-10: E75.24 Clinical summary This genetic test evaluates the NPC1 gene for pathogenic variants associated with Niemann-Pick disease type C1.
TEST-3909 NR1H4 Gene Sequencing for Infantile Cholestasis (NR1H4‑Related) Test This test evaluates the NR1H4 gene for pathogenic variants associated with infantile cholestasis and PFIC5.	Whole Blood (EDTA), Extracted DNA, 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 NR1H4 gene", "Coding exons and splice sites"] Parameters [] Preparation [] Indications ["Infantile cholestasis", "Progressive Familial Intrahepatic Cholestasis type 5 (PFIC5)"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: K76.8 Clinical summary This test evaluates the NR1H4 gene for pathogenic variants associated with infantile cholestasis and PFIC5.
TEST-3408 NSMF Gene Hypogonadotropic Hypogonadism Genetic Test This genetic test identifies pathogenic variants in the NSMF gene associated with congenital hypogonadotropic hypogonadism (CHH).	Whole Blood (Peripheral)	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 NSMF gene", "Single nucleotide variants (SNVs)", "Insertions/deletions (indels)", "Copy number variations (CNVs)"] Parameters [] Preparation [] Indications ["Patients with absent/delayed puberty", "Amenorrhea in females", "Small testes in males", "Infertility of unknown origin", "Family history of Kallmann syndrome or unexplained CHH"] Measurement technique Confirm with laboratory Codes LOINC: 81265-2 ICD-10: E23.0, Q87.8 Clinical summary This genetic test identifies pathogenic variants in the NSMF gene associated with congenital hypogonadotropic hypogonadism (CHH).
TEST-4989 NSUN2 Gene Mental Retardation, Autosomal Recessive Type 5 Genetic Test This test analyzes the NSUN2 gene to detect pathogenic variants associated with autosomal recessive intellectual disability type 5.	Peripheral Whole Blood, Extracted DNA, or FTA Card Blood Spot	15–20 Business Days	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the NSUN2 gene", "Single nucleotide variants", "Insertions", "Deletions", "Splice-site alterations"] Parameters [] Preparation [] Indications ["Clinical suspicion of autosomal recessive intellectual disability type 5", "Family history of intellectual disability", "Need for definitive molecular diagnosis for genetic counseling"] Measurement technique Confirm with laboratory Codes LOINC: 81413-9 ICD-10: F78.9 Clinical summary This test analyzes the NSUN2 gene to detect pathogenic variants associated with autosomal recessive intellectual disability type 5.
TEST-2707 Nx Gen Sequencing: Alkaptonuria Test This test identifies disease-causing variants in the HGD gene to confirm a molecular diagnosis of alkaptonuria.	Peripheral Whole Blood	40 working days	2,600.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic and likely pathogenic variants in the HGD gene", "Single-nucleotide variants", "Small insertions and deletions", "Splice-site alterations"] Parameters [] Preparation ["Mandatory pre-test genetic counselling session", "Written informed consent using the Whole Exome Sequencing Consent Form (Form 37) is mandatory"] Indications ["Suspected alkaptonuria", "Ochronotic arthropathy", "Unexplained homogentisic aciduria", "Differentiation from other tyrosine metabolism disorders", "Carrier status assessment"] Measurement technique Confirm with laboratory Codes LOINC: 88040-2 ICD-10: E70.29 Clinical summary This test identifies disease-causing variants in the HGD gene to confirm a molecular diagnosis of alkaptonuria.
TEST-2745 NxGen Sequencing for Dravet Syndrome & Early Infantile Epileptic Encephalopathy (EIEE) Test This diagnostic test evaluates for pathogenic variants in genes associated with Dravet syndrome and Early Infantile Epileptic Encephalopathies (EIEE).	Peripheral Whole Blood (10 mL in Lavender-Top EDTA Tubes)	40 Working Days	2,600.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in SCN1A, PCDH19, STXBP1, CDKL5, KCNQ2, ARX, and other associated genes", "Copy Number Variants (CNVs) in target genes"] Parameters [{"name": "Method", "reference_range": "NGS + Sanger Confirmation"}, {"name": "Genes Analyzed", "reference_range": "SCN1A, PCDH19, STXBP1, CDKL5, KCNQ2, ARX, and more"}, {"name": "Detection of Copy Number Variants", "reference_range": "Yes, via NGS depth-based analysis"}] Preparation ["No specific fasting required", "Continue all prescribed medications unless otherwise directed by your physician"] Indications ["Suspected Dravet syndrome", "Suspected Early Infantile Epileptic Encephalopathy (EIEE)", "Unexplained early-onset seizures", "Family history of Dravet syndrome or EIEE"] Measurement technique Confirm with laboratory Codes LOINC: 95406-2 ICD-10: G40.83, G40.4 Clinical summary This diagnostic test evaluates for pathogenic variants in genes associated with Dravet syndrome and Early Infantile Epileptic Encephalopathies (EIEE).
TEST-2599 ORC1 Gene Meier-Gorlin Syndrome Type 1 Genetic Test This genetic test detects pathogenic variants in the ORC1 gene, which are linked to Meier-Gorlin syndrome type 1.	Whole Blood (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 ["Pathogenic variants in the ORC1 gene", "Coverage of ORC1 gene including regulatory regions"] Parameters [] Preparation [] Indications ["Suspected Meier-Gorlin syndrome type 1", "Clinical diagnosis in children with dysmorphology", "Differentiation from other growth-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q87.1 Clinical summary This genetic test detects pathogenic variants in the ORC1 gene, which are linked to Meier-Gorlin syndrome type 1.
TEST-4813 PACS1 Gene Sequencing (Intellectual Disability, Autosomal Dominant Type 17) Genetic Test This test evaluates the PACS1 gene for pathogenic variants associated with autosomal dominant intellectual disability type 17.	Peripheral whole blood (EDTA) or dried blood spot (FTA card)	21–28 business days (3–4 weeks)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic single-nucleotide variants in PACS1", "Small insertions/deletions in PACS1", "Copy Number Variations (CNV) in PACS1"] Parameters [] Preparation ["Genetic counselling & pedigree drawing included"] Indications ["Children with unexplained global developmental delay", "Children with dysmorphic features", "Children with seizures", "Inconclusive metabolic and chromosomal evaluations"] Measurement technique Confirm with laboratory Codes LOINC: 59042-0 ICD-10: Q87.89 Clinical summary This test evaluates the PACS1 gene for pathogenic variants associated with autosomal dominant intellectual disability type 17.
TEST-6287 PALB2 Gene Fanconi Anemia Type N Genetic Test (NGS) This test identifies pathogenic variants in the PALB2 gene associated with Fanconi anemia type N and increased risk for hereditary breast and pancreatic cancers.	Peripheral Whole Blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic germline variants in the PALB2 gene", "Full coding region ± 20 bp intronic boundaries"] Parameters [] Preparation ["No specific preparation required"] Indications ["Diagnosis of Fanconi anemia type N", "Assessment of hereditary breast and pancreatic cancer risk"] Measurement technique Confirm with laboratory Codes LOINC: 21666-7 ICD-10: D61.09 Clinical summary This test identifies pathogenic variants in the PALB2 gene associated with Fanconi anemia type N and increased risk for hereditary breast and pancreatic cancers.
TEST-3744 PAX8 Gene Hypothyroidism, Congenital Nongoitrous Type 2, Familial Test This genetic test evaluates the PAX8 gene for pathogenic variants associated with congenital non-goitrous hypothyroidism type 2.	Whole blood (EDTA) or Buccal swab (DNA FTA card)	3 – 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PAX8 gene variants", "Pathogenic mutations"] Parameters [] Preparation ["Avoid biotin supplements and high-dose vitamin B7 for 24 hours before blood draw.", "Mandatory genetic counselling session prior to sample collection."] Indications ["Suspected congenital non-goitrous hypothyroidism type 2", "Family history of the disorder", "Need for genetic confirmation"] Measurement technique Confirm with laboratory Codes LOINC: 21601-8 ICD-10: E03.1 Clinical summary This genetic test evaluates the PAX8 gene for pathogenic variants associated with congenital non-goitrous hypothyroidism type 2.
TEST-3803 PFN1 Gene Sequencing for Amyotrophic Lateral Sclerosis Type 18 (ALS18) Test This test analyzes the entire PFN1 gene for mutations linked to Amyotrophic Lateral Sclerosis type 18 (ALS18).	Whole Blood (EDTA)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["PFN1 gene mutations", "Pathogenic variants"] Parameters [] Preparation ["No fasting required"] Indications ["Individuals with a family history of motor neuron disease", "Unexplained progressive muscle weakness", "Known PFN1 mutation in relatives"] Measurement technique Confirm with laboratory Codes LOINC: 21612-4 ICD-10: G12.21 Clinical summary This test analyzes the entire PFN1 gene for mutations linked to Amyotrophic Lateral Sclerosis type 18 (ALS18).
TEST-2564 PHC1 Gene Microcephaly Autosomal Recessive Type 11 Genetic Test This test identifies pathogenic mutations in the PHC1 gene associated with autosomal recessive microcephaly type 11.	Peripheral whole blood (venous or capillary)	3–4 weeks (priority processing)	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic mutations in the PHC1 gene"] Parameters [] Preparation [] Indications ["Children presenting with microcephaly", "Newborns with suspected genetic microcephaly", "Families with a history of the condition"] Measurement technique Confirm with laboratory Codes LOINC: 21726-5 ICD-10: Q02 Clinical summary This test identifies pathogenic mutations in the PHC1 gene associated with autosomal recessive microcephaly type 11.

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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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.