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Results: 1 to 20 of 35 (representing 25 labs)

Tests names and labsConditionsGenes and analytesMethods

Mitochondrial genome panel

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

Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel

Otogenetics
United States
124129
  • E Sequence analysis of select exons

Mitochondrial dysfunctions panel

Centogene AG - the Rare Disease Company
Germany
122
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MERRF/MELAS overlap syndrome

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Mitochondrial Hearing Loss - MTTS1 Gene

Center for Genetics at Saint Francis Saint Francis Hospital
United States
11
  • C Sequence analysis of the entire coding region

Mitochondrial Genome Sequence

Molecular Genetics Laboratory London Health Sciences Centre
Canada
2238
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

MT-TS1. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

OtoGenome Test for Hearing Loss (87 Genes)

Laboratory for Molecular Medicine Laboratory for Molecular Medicine (Partners HealthCare Personalized Medicine)
United States
11286
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Mitochondrial DNA Hearing Loss Panel (2 genes)

Laboratory for Molecular Medicine Laboratory for Molecular Medicine (Partners HealthCare Personalized Medicine)
United States
22
  • C Sequence analysis of the entire coding region

Mitochondrial Disorders Panel (mtDNA Sequencing and Deletion/Duplication, 121 Nuclear Genes Sequencing, 119 Nuclear Genes Deletion/Duplication)

ARUP Laboratories, Molecular Genetics and Genomics
United States
1157
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

OtoSCOPE

Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics
United States
98147
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Mitochondrial Genome NGS Panel

Fulgent Genetics
United States
237
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Mitochondrial Metabolic Panel

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health and Science University
United States
4196
  • C Sequence analysis of the entire coding region

MT-TS1

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

NGS Hearing Loss Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
11091
  • C Sequence analysis of the entire coding region

Mitochondrial complex IV deficiency

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
414
  • C Sequence analysis of the entire coding region

USHER SYNDROME and NON-SYNDROMIC DEAFNESS

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
2518
  • C Sequence analysis of the entire coding region

Mitochondrial nonsyndromic sensorineural deafness

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Dilated Cardiomyopathy Panel

ApolloGen, Inc.
United States
133
  • E Sequence analysis of select exons

Comprehensive Cardiomyopathy Panel

ApolloGen, Inc.
United States
144
  • E Sequence analysis of select exons

Results: 1 to 20 of 35

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.

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