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Results: 1 to 20 of 70 (representing 23 labs)

Tests names and labsConditionsGenes and analytesMethods

CentoICU platinum

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

CentoICU platinum plus

Centogene AG - the Rare Disease Company
Germany
769514
  • 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

CMT1E

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

Charcot Marie Tooth Type 1A

Molecular Genetics Laboratory London Health Sciences Centre
Canada
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hereditary Neuropathy with Liability to Pressure Palsies (PMP22)

Molecular Genetics Laboratory London Health Sciences Centre
Canada
31
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

CMT Type1E, PMP22

Molecular Genetics Laboratory London Health Sciences Centre
Canada
11
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Comprehensive Neuropathy Sequencing Panel

PreventionGenetics
United States
8271
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Charcot Marie Tooth - Comprehensive Sequencing Panel

PreventionGenetics
United States
5445
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Charcot Marie Tooth - Demyelinating Neuropathy Sequencing Panel

PreventionGenetics
United States
3525
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Charcot Marie Tooth Panel

Molecular Genetics Laboratory London Health Sciences Centre
Canada
4634
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

PMP22-Related Neuropathies

PreventionGenetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

DNM2, GARS, GDAP1, GJB1, MFN2, MPZ, MTMR2, NEFL, PMP22, PRX. NextGeneDx.Complete sequencing by NGS

Instituto de Medicina Genomica
Spain
1810
  • C Sequence analysis of the entire coding region

Peripheral Myelin Protein 22 (PMP22) gene sequencing test

Neurogenetics Department Cyprus Institute of Neurology and Genetics
Cyprus
11
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth neuropathy demyelinating panel

LifeLabs Genetics
Canada
1715
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CMT Advanced Evaluation - Nonprevalent Demyelinating

Athena Diagnostics Inc
United States
1714
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CMT Advanced Evaluation - Nonprevalent

Athena Diagnostics Inc
United States
2521
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CMT Advanced Evaluation - Initial Genetic Assessment

Athena Diagnostics Inc
United States
84
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Comprehensive Neuropathies Panel

Invitae
United States
10070
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Single gene testing PMP22

CeGaT GmbH
Germany
61
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 70

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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