Diagnostic options · UAE

Genetics tests in Dubai & UAE

Compare available Genetics tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

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2,789

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-1.00–50,000.00 AED

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Genetics test prices

Showing 421–435 of 2,789 matching tests.

Genetics diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-5010 CDSN Gene Hypotrichosis Type 2 Genetic Test This test detects pathogenic variants in the CDSN gene associated with autosomal recessive hypotrichosis type 2.	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 ["Pathogenic variants in the CDSN gene"] Parameters [] Preparation ["No special preparation required", "Provide detailed clinical history", "Pre-test genetic counseling recommended"] Indications ["Diagnosis of autosomal recessive hypotrichosis type 2", "Carrier screening", "Family planning guidance", "Differential diagnosis"] Measurement technique Confirm with laboratory Codes LOINC: 92039-4 ICD-10: Q84.0 Clinical summary This test detects pathogenic variants in the CDSN gene associated with autosomal recessive hypotrichosis type 2.
TEST-4666 CDSN Gene Peeling Skin Syndrome Type 1 Genetic Test This genetic test analyzes the CDSN gene to detect mutations associated with Peeling Skin Syndrome Type 1.	Whole Blood, Extracted DNA, FTA Card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CDSN gene sequence", "Pathogenic variants (point mutations, indels, splice variants, CNVs)"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any current anticoagulant therapy"] Indications ["Suspected Peeling Skin Syndrome Type 1", "Family history of Peeling Skin Syndrome Type 1"] Measurement technique Confirm with laboratory Codes LOINC: 94229-4 ICD-10: Q82.8 Clinical summary This genetic test analyzes the CDSN gene to detect mutations associated with Peeling Skin Syndrome Type 1.
TEST-2594 CDT1 Gene Meier‑Gorlin Syndrome Type 4 Genetic Test This genetic test identifies pathogenic variants in the CDT1 gene, confirming Meier‑Gorlin syndrome type 4.	Whole blood (EDTA, 1–2 mL) or FTA card	3 – 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CDT1 gene pathogenic variants", "Copy Number Variants (CNVs) in CDT1"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medication without consulting your physician"] Indications ["Suspected diagnosis of Meier‑Gorlin syndrome type 4", "Genetic confirmation for family planning"] Measurement technique Confirm with laboratory Codes LOINC: 81225-0 ICD-10: Q87.1 Clinical summary This genetic test identifies pathogenic variants in the CDT1 gene, confirming Meier‑Gorlin syndrome type 4.
TEST-5680 CEACAM16 Gene Deafness Autosomal Dominant Type 4B Genetic Test This test identifies pathogenic variants in the CEACAM16 gene associated with autosomal dominant deafness type 4B.	Whole Blood (EDTA), DNA Extract, 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 CEACAM16 gene", "Copy Number Variations (CNV) in the CEACAM16 gene"] Parameters [] Preparation ["No fasting required", "No medication changes required"] Indications ["Suspected autosomal dominant deafness type 4B", "Family history of hearing loss", "Genetic counseling for hearing loss"] Measurement technique Confirm with laboratory Codes LOINC: 55233-1 ICD-10: H90.5 Clinical summary This test identifies pathogenic variants in the CEACAM16 gene associated with autosomal dominant deafness type 4B.
TEST-2019 CEBPA Gene Somatic Mutation Analysis (NGS) for Acute Myeloid Leukemia (AML) Test This test identifies somatic mutations in the CEBPA gene using Next-Generation Sequencing (NGS) from blood, DNA, or FTA cards.	Whole 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 ["Somatic mutations in the CEBPA gene", "Variant Allele Frequency (VAF)"] Parameters [] Preparation [] Indications ["Diagnosis of Acute Myeloid Leukemia (AML)", "Risk stratification in AML", "Personalized treatment planning in AML"] Measurement technique Confirm with laboratory Codes LOINC: 69548-6 ICD-10: C92.00, C92.01, Z15.09 Clinical summary This test identifies somatic mutations in the CEBPA gene using Next-Generation Sequencing (NGS) from blood, DNA, or FTA cards.
TEST-3915 CELF6 Gene Genetic Test for Autism Spectrum Disorder This test identifies pathogenic variants in the CELF6 gene associated with Autism Spectrum Disorder (ASD).	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 variants in the CELF6 gene", "Single-nucleotide variants", "Small insertions", "Small deletions"] Parameters [] Preparation [] Indications ["Diagnosis of Autism Spectrum Disorder", "Family history of ASD", "Genetic counseling for ASD"] Measurement technique Confirm with laboratory Codes LOINC: 94473-2 ICD-10: F84.0 Clinical summary This test identifies pathogenic variants in the CELF6 gene associated with Autism Spectrum Disorder (ASD).
TEST-5666 CELSR2 Gene Genetic Testing for Schizophrenia Risk Assessment Test This test evaluates the CELSR2 gene for variants associated with an increased risk of developing schizophrenia spectrum disorders.	Whole Blood (EDTA), Extracted DNA, 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 ["CELSR2 gene sequence", "Single nucleotide variants (SNVs)", "Small insertions/deletions", "Copy-number alterations", "Regulatory regions of CELSR2"] Parameters [] Preparation ["Mandatory pre-test genetic counselling session required.", "No fasting or medication changes needed.", "Informed consent required."] Indications ["Familial schizophrenia pedigree", "Treatment-resistant psychosis of unclear aetiology", "Differential diagnosis of schizoaffective versus neurodevelopmental disorder", "Pre-symptomatic risk profiling in first-degree relatives"] Measurement technique Confirm with laboratory Codes LOINC: 81409-6 ICD-10: Z13.89 Clinical summary This test evaluates the CELSR2 gene for variants associated with an increased risk of developing schizophrenia spectrum disorders.
TEST-2560 CENPE Gene Autosomal Recessive Primary Microcephaly Type 13 Genetic Test This test evaluates the CENPE gene for mutations associated with autosomal recessive primary microcephaly type 13.	Peripheral whole blood (3–5 mL in EDTA tube) or FTA card	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["CENPE gene sequence", "Pathogenic variants in CENPE"] Parameters [] Preparation ["No fasting required", "Keep child hydrated", "Avoid creams on venipuncture site"] Indications ["Suspected diagnosis of autosomal recessive primary microcephaly type 13", "Family history of MCPH13"] Measurement technique Confirm with laboratory Codes LOINC: 81319-2 ICD-10: Q02 Clinical summary This test evaluates the CENPE gene for mutations associated with autosomal recessive primary microcephaly type 13.
TEST-2550 CENPJ Gene (MCPH6) Genetic Test This test identifies pathogenic variants in the CENPJ gene, confirming a diagnosis of autosomal recessive primary microcephaly type 6 (MCPH6).	Blood / FTA Card / 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 CENPJ gene"] Parameters [] Preparation [] Indications ["Diagnosis of autosomal recessive primary microcephaly type 6 (MCPH6)", "Carrier status determination", "Genetic counseling for families with MCPH6"] Measurement technique Confirm with laboratory Codes LOINC: 81265-5 ICD-10: Q02 Clinical summary This test identifies pathogenic variants in the CENPJ gene, confirming a diagnosis of autosomal recessive primary microcephaly type 6 (MCPH6).
TEST-2353 CENPJ Gene Seckel Syndrome Type 4 Genetic Test This test identifies pathogenic variants in the CENPJ gene associated with Seckel syndrome type 4.	Whole Blood (EDTA), Extracted DNA, or FTA Card	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 CENPJ gene", "Single nucleotide variants", "Insertions/deletions", "Copy number variants"] Parameters [] Preparation ["No fasting required", "Report recent blood transfusions"] Indications ["Suspected Seckel syndrome type 4", "Pediatric cases with characteristic features", "Recurrence risk assessment", "Family planning"] Measurement technique Confirm with laboratory Codes LOINC: 95209-3 ICD-10: Q87.1 Clinical summary This test identifies pathogenic variants in the CENPJ gene associated with Seckel syndrome type 4.
TEST-2545 CEP135 Gene Sequencing for Autosomal Recessive Primary Microcephaly Type 8 (MCPH8) Test This diagnostic test evaluates the CEP135 gene for pathogenic variants associated with autosomal recessive primary microcephaly type 8 (MCPH8).	Peripheral Whole Blood (3–5 mL in 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 CEP135 gene", "Copy Number Variations (CNV) in CEP135"] Parameters [] Preparation ["Provide a detailed family history", "Have previous medical reports ready for genetic counseling"] Indications ["Clinical suspicion of primary microcephaly type 8", "Family history of MCPH8", "Genetic counseling for families with microcephaly"] Measurement technique Confirm with laboratory Codes LOINC: 51968-1 ICD-10: Q02 Clinical summary This diagnostic test evaluates the CEP135 gene for pathogenic variants associated with autosomal recessive primary microcephaly type 8 (MCPH8).
TEST-2552 CEP152 Gene Microcephaly (Autosomal Recessive Type 9) Genetic Test This genetic test identifies pathogenic variants in the CEP152 gene associated with autosomal recessive primary microcephaly type 9.	Whole blood (3–5 mL in EDTA tube), DNA FTA card, or extracted DNA	3 to 4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the CEP152 gene"] Parameters [] Preparation ["Clinical history documentation", "Pre-test genetic counselling session", "Three-generation pedigree chart"] Indications ["Suspected primary microcephaly type 9", "Family history of microcephaly", "Genetic counselling for reproductive planning"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: Q02 Clinical summary This genetic test identifies pathogenic variants in the CEP152 gene associated with autosomal recessive primary microcephaly type 9.
TEST-3614 CEP164 Gene Nephronophthisis Type 15 Genetic Test This test analyzes the CEP164 gene for mutations associated with Nephronophthisis type 15, a genetic disorder affecting multiple organs.	Peripheral whole blood (2–5 mL in EDTA tube) or FTA card blood spot; alternative: extracted DNA (≥1 µg)	14–21 working days 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 CEP164 gene", "Coding exons and flanking intronic regions of CEP164"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any recent bone marrow transplant or stem cell therapy"] Indications ["Suspected Nephronophthisis type 15", "Family history of ciliopathies", "Genetic counselling for family planning"] Measurement technique Confirm with laboratory Codes LOINC: 81247-4 ICD-10: Q61.8, Z13.79, Z14.8 Clinical summary This test analyzes the CEP164 gene for mutations associated with Nephronophthisis type 15, a genetic disorder affecting multiple organs.
TEST-3687 CEP290 Gene Meckel Syndrome Type 4 Genetic Test This test detects pathogenic variants in the CEP290 gene associated with Meckel syndrome type 4.	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 CEP290 gene"] Parameters [] Preparation ["None specified"] Indications ["Suspected Meckel syndrome type 4", "Family history of Meckel syndrome type 4", "Genetic counseling for family planning"] Measurement technique Confirm with laboratory Codes LOINC: 82939-0 ICD-10: Q61.8 Clinical summary This test detects pathogenic variants in the CEP290 gene associated with Meckel syndrome type 4.
TEST-3519 CEP290 Gene Senior-Loken Syndrome Type 6 Genetic Test This test identifies pathogenic variants in the CEP290 gene associated with Senior-Loken syndrome type 6, characterized by kidney disease and vision loss.	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 variants in CEP290 gene", "Coding exons", "Intron-exon boundaries", "Conserved splice-site regions"] Parameters [] Preparation ["No fasting required", "Pre-test genetic counseling session is mandatory", "Parental consent required for minors"] Indications ["Suspected Senior-Loken syndrome type 6", "Family history of ciliopathy", "Need for genetic confirmation"] Measurement technique Confirm with laboratory Codes LOINC: 81301-3 ICD-10: Q87.8, H35.5, Z14.8 Clinical summary This test identifies pathogenic variants in the CEP290 gene associated with Senior-Loken syndrome type 6, characterized by kidney disease and vision loss.

Category overview

Genetics: overview

Understanding your unique biological blueprint offers a profound sense of clarity and empowers proactive health planning for you and your family. At DNA Labs UAE, our specialized Genetics division employs state-of-the-art molecular technologies to provide deep insights into hereditary markers and cellular mutations. This comprehensive genetics testing in the UAE equips your healthcare provider with the precise data needed to tailor your medical guidance effectively. Recognized among top diagnostic labs in Dubai and the UAE, we prioritize your peace of mind through strict confidentiality protocols and exceptionally fast, accurate reporting. Take the next step in your health journey. View our genetics diagnostic services, book a private home collection, or consult our specialized team today.

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Genetics tests in Dubai & UAE

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