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Results: 1 to 20 of 48

Tests names and labsConditionsGenes, analytes, and microbesMethods

Birt-Hogg-Dube syndrome NGS Test

HNL Genomics Connective Tissue Gene Tests
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Aminoglycoside-Induced Hearing Loss Panel

Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics
United States
73
  • T Targeted variant analysis

Mitochondrial Non Syndromic Hearing Loss and Deafness

Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS
Chile
14
  • T Targeted variant analysis

mtRNR1 gene sequencing for hearing loss

Molecular Diagnostics Children's Hospital of Wisconsin
United States
23
  • T Targeted variant analysis

Mitochondrial genome panel

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

MT-RNR1 Gene Deafness, nonsyndromic, sensorineural, mitochondrial 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
287218
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel

Otogenetics
United States
122128
  • E Sequence analysis of select exons

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

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

AudioloGene Hearing Loss Panel

Mayo Clinic Laboratories Mayo Clinic
United States
1200
  • C Sequence analysis of the entire coding region

PGx-Premium (Preemptive PGx test)

SPMED CO., LTD Step forward Personalized Medicine
South Korea
6627
  • T Targeted variant analysis

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

Pharmacogenomics SNaP-Shot

Ariel Precision Medicine
United States
126
  • T Targeted variant analysis

PGmito - Mitochondrial Genome Sequencing

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

Hearing Loss Panel

Molecular Diagnostics Children's Hospital of Wisconsin
United States
95
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Results: 1 to 20 of 48

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.