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Results: 21 to 40 of 43

Tests names and labsConditionsGenes, analytes, and microbesMethods

Comprehensive Hearing Loss + mtDNA

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
218300
  • C Sequence analysis of the entire coding region

Genomic Unity® Retinal Disorders Analysis

Variantyx, Inc.
United States
1394
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Metabolic Diseases Panel

CGC Genetics Unilabs
Portugal
1837
  • C Sequence analysis of the entire coding region

Leber optic atrophy (sequence analysis of MTND6 gene)

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

Mitochondrial Diseases Panel (Nuclear and Mitochondrial DNA)

Mendelics
Brazil
1169
  • 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

LHON Gene Analysis

Duzen Laboratories Duzen BBAGUAS
Turkey
13
  • T Targeted variant analysis

Rapid MitoGenome Seq + Del

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
137
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MitoGenome Seq + Del

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
137
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Maternal MitoGenome Seq + Del

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
137
  • C Sequence analysis of the entire coding region

Combined Cardiac Sequencing and Del/Dup Panel

GeneDx
United States
10138
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MT-ND6

Institute for Human Genetics University Medical Center Freiburg
Germany
11
  • C Sequence analysis of the entire coding region

Mitochondrial Genome NGS Panel

Fulgent Genetics
United States
137
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Single gene testing MT-ND6

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Leber's hereditary optic neuropathy

Centre for cellular and molecular biology Centre for Cellular and Molecular Biology
India
11
  • T Targeted variant analysis

mtDNA encoded Mitochondriopathies Panel

CeGaT GmbH
Germany
1137
  • C Sequence analysis of the entire coding region

Nuclear encoded Mitochondriopathies Panel

CeGaT GmbH
Germany
37284
  • C Sequence analysis of the entire coding region

LHON, MT-ND1, MT-MD4, MT-ND6 Sequencing

Molecular Diagnostics Laboratory Seoul National University Hospital
South Korea
13
  • C Sequence analysis of the entire coding region

Leber Optic Atrophie

MedGene
Slovakia
14
  • E Sequence analysis of select exons

Leber Optic Atrophie

Praxis fuer Humangenetik Wien
Austria
14
  • E Sequence analysis of select exons

Results: 21 to 40 of 43

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.