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Results: 1 to 20 of 42

Tests names and labsConditionsGenes, analytes, and microbesMethods

OtoSCOPE v9

Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics
United States
288218
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel

Otogenetics
United States
123129
  • E Sequence analysis of select exons

Mitochondrial Genome Sequencing and Depletion/Integrity Panel

Molecular Genetics Laboratory London Health Sciences Centre
Canada
4852
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Juvenile myopathy, encephalopathy, lactic acidosis AND stroke (MELAS)

Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS
Chile
12
  • T Targeted variant analysis

Mitochondrial Full Genome Analysis

Mayo Clinic Laboratories Mayo Clinic
United States
2937
  • C Sequence analysis of the entire coding region

PGmito - Mitochondrial Genome Sequencing

PreventionGenetics, part of Exact Sciences
United States
1638
  • C Sequence analysis of the entire coding region

mtDNA - mitochondriopathy (MELAS)

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
11
  • C Sequence analysis of the entire coding region

mtDNA - mitochondriopathy (encephalopathy)

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
11
  • C Sequence analysis of the entire coding region

MELAS m.3243A>G

Inherited Metabolic Disease group University of Cape Town and National Health Laboratory Services
South Africa
21
  • T Targeted variant analysis

MELAS syndrome (sequence analysis of MTTF gene)

CGC Genetics Unilabs
Portugal
11
  • C Sequence analysis of the entire coding region

MELAS syndrome (sequence analysis of MTTL1 gene)

CGC Genetics Unilabs
Portugal
11
  • C Sequence analysis of the entire coding region

Mitochondrial Disorders Panel

Dhiti Omics Technologies Private Ltd
India
2837
  • C Sequence analysis of the entire coding region

Melas Syndrome (A3243G)

Duzen Laboratories Duzen BBAGUAS
Turkey
11
  • T Targeted variant analysis

Melas Syndrome (A3243G, T3271C, A3252G)

Duzen Laboratories Duzen BBAGUAS
Turkey
11
  • T Targeted variant analysis

Melas Syndrome (MTTL1 Gene Sequence Analysis)

Duzen Laboratories Duzen BBAGUAS
Turkey
11
  • C Sequence analysis of the entire coding region

mtDNA Targeted Analysis: Known Familial Mutation

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
1134
  • T Targeted variant analysis

mtDNA Targeted Analysis with Heteroplasmy: Known Familial Mutation

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
1134
  • T Targeted variant analysis

Common 29 mtDNA Variant Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
932
  • T Targeted variant analysis

Expanded 93 mtDNA Variant Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
1134
  • T Targeted variant analysis

Stroke (NGS Panel and Copy Number Analysis + mtDNA)

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
385
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 42

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.