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Results: 1 to 20 of 28

Tests names and labsConditionsGenes, analytes, and microbesMethods

Mitochondrial genome panel

Centogene AG - the Rare Disease Company
Germany
137
  • C Sequence analysis of the entire coding region

MT-ND5 Gene Leigh syndrome due to mitochondrial complex I deficiency NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

MT-ND5 Gene Mitochondrial complex I deficiency NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

Genomic Unity® Hearing Loss Disorders Analysis

Variantyx, Inc.
United States
1318
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

MVL Vision Panel

Molecular Vision Laboratory
United States
13581028
  • C Sequence analysis of the entire coding region

Mitochondrial Full Genome Analysis

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

Congenital Lactic Acidosis Panel

Mayo Clinic Laboratories Mayo Clinic
United States
165
  • D Deletion/duplication analysis
  • 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

MVL Vision Panel

Molecular Vision Laboratory
United States
342268
  • C Sequence analysis of the entire coding region

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 MTND5 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

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

LEBER HEREDITARY OPTIC NEUROPATHY (LHON)

Laboratorio de Genetica Clinica SL
Spain
112
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Results: 1 to 20 of 28

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.