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Results: 1 to 20 of 50

Tests names and labsConditionsGenes and analytesMethods

Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel

Otogenetics
United States
124129
  • E Sequence analysis of select exons

mtRNR1 gene sequencing for hearing loss

Molecular Diagnostics Children's Hospital of Wisconsin
United States
21
  • T Targeted variant analysis

Hearing Loss Panel

Molecular Diagnostics Children's Hospital of Wisconsin
United States
94
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

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-TH. Complete sequencing

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

MT-CO1. Complete sequencing

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

MTTH. Complete sequencing

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

MT-TS1. Complete sequencing

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

MTCO1. Complete sequencing

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

OtoGenome Test for Hearing Loss (110 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
23110
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Mitochondrial Non Syndromic Hearing Loss and Deafness

Molecular Genetics and Cytogenetics, Clinical Laboratory Service Faculty of Medicine, Pontificia Universidad Católica de Chile
Chile
13
  • T Targeted variant analysis

OtoSCOPE

Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics
United States
181153
  • D Deletion/duplication analysis
  • 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 nonsyndromic sensorineural deafness

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

Mitochondrial nonsyndromic sensorineural deafness

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

Mitochondrial nonsyndromic sensorineural deafness

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

Familiar hereditary deafness

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

Mitochondrial nonsyndromic sensorineural deafness

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

Congenital mitochondrial deafness (961delT/insC mutation on MTRNR1 gene)

CGC Genetics
Portugal
11
  • T Targeted variant analysis

Mitochondrial dealfness (mutation T1095C, A1555G, A3243G, A7445G, 7472insC, T7510C and T7511C)

CGC Genetics
Portugal
11
  • T Targeted variant analysis

Results: 1 to 20 of 50

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