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Results: 1 to 20 of 39

Tests names and labsConditionsGenes and analytesMethods

AllNeuro panel

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

CMT4B2

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

Hereditary Myeloid Malignancy and Inherited Bone Marrow Failure Panel

Genetic Services Laboratory University of Chicago
United States
3679
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth Type 4B2 via the SBF2 Gene

PreventionGenetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

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 - Axonal Neuropathy Sequencing Panel

PreventionGenetics
United States
4738
  • 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

Charcot-Marie-Tooth

Human Genetics University Hospital Bern
Switzerland
2322
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CHARCOT-MARIE-TOOTH : NGS PANEL

Laboratorio de Genetica Clinica SL
Spain
4034
  • C Sequence analysis of the entire coding region

CHARCOT-MARIE-TOOTH DISEASE TYPE 4B2

Laboratorio de Genetica Clinica SL
Spain
11
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth Disease Type 4 , Deletions-Duplications (MLPA) GDAP1,MTMR2,SBF2,PRX,SH3TC2 Genes

Reference Laboratory Genetics
Spain
55
  • D Deletion/duplication analysis

Charcot-Marie-Tooth Disease Type 4B2 , Sequencing SBF2 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Glaucoma

Asper Biogene Asper Biogene LLC
Estonia
1920
  • 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

Invitae Comprehensive Neuropathies Panel

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

Glaucoma (Advance)

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
3734
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 39

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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