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Results: 1 to 20 of 29 (representing 18 labs)

Tests names and labsConditionsGenes and analytesMethods

AllNeuro panel

Centogene AG - the Rare Disease Company
Germany
7861205
  • C Sequence analysis of the entire coding region

HSAN1

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • 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

Hereditary Sensory and Autonomic Neuropathy Sequencing Panel

PreventionGenetics
United States
1212
  • 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

SPTLC1. Complete sequencing

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

Charcot-Marie-Tooth Neuropathy Panel

Blueprint Genetics
Finland
186
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth Syndrome

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health and Science University
United States
534
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SPTLC1

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

Invitae Hereditary Sensory and Autonomic Neuropathy Panel

Invitae
United States
1817
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Comprehensive Neuropathies Panel

Invitae
United States
10779
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary sensory and autonomic neuropathy type 1A

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

Charcot-Marie-Tooth (CMT) and Related Hereditary Neuropathies Panel Sequencing

ARUP Laboratories, Molecular Genetics and Genomics
United States
3478
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth (CMT) and Related Hereditary Neuropathies, PMP22 Deletion/Duplication with Reflex to Sequencing Panel

ARUP Laboratories, Molecular Genetics and Genomics
United States
3478
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Single gene testing SPTLC1

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Hereditary peripheral neuropathies, including Charcot-Marie-Tooth disease (NGS panel for 74 genes)

CGC Genetics
Portugal
174
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth and Sensory Neuropathies Panel

CeGaT GmbH
Germany
6484
  • C Sequence analysis of the entire coding region

SPTLC1 - Gene sequencing

Clinical Genetics Academic Medical Center
Netherlands
11
  • C Sequence analysis of the entire coding region

Neuropathy

Medizinisch Genetisches Zentrum München MGZ München
Germany
7122
  • C Sequence analysis of the entire coding region

SPTLC1

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 29

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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