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Results: 1 to 20 of 41

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-TK Gene MERRF syndrome, MT-TK related NGS Genetic DNA Test

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

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

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

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

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

MERRF syndrome (sequence analysis of A8344G mutation on MT-TK gene)

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

Sequence analysis of MT-TK 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

MERRF Syndrome (A8344G, T8356C, G8363A and G8361A) Analysis

Duzen Laboratories Duzen BBAGUAS
Turkey
11
  • T Targeted variant analysis

MERRF Syndrome (A8344G)

Duzen Laboratories Duzen BBAGUAS
Turkey
11
  • T Targeted variant analysis

Rest of Combined Cardiac after ARVC Panel

GeneDx
United States
5121
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Rest of Combined Cardiac after Arrhythmia Panel

GeneDx
United States
580
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 41

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.