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Results: 41 to 54 of 54

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hereditary Spastic Paraplegias (HSP) and differential diagnoses Panel

CeGaT GmbH
Germany
147143
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth Disease

Asper Biogene Asper Biogene LLC
Estonia
8974
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Mitochondrial Diseases (mtDNA and 217 nuclear genes)

Asper Biogene Asper Biogene LLC
Estonia
89210
  • C Sequence analysis of the entire coding region

GARS Single Gene

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Charcot Marie Tooth Disease Extended NGS Panel

Fulgent Genetics
United States
17259
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Distal Hereditary Motor Neuropathy NGS Panel

Fulgent Genetics
United States
3815
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

GARS (CMT2D) DNA Sequencing Test

Athena Diagnostics Inc
United States
11
  • C Sequence analysis of the entire coding region

CMT Advanced Evaluation - Axonal

Athena Diagnostics Inc
United States
2013
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CMT Advanced Evaluation - Comprehensive

Athena Diagnostics Inc
United States
3123
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CMT Advanced Evaluation - Dominant, Axonal

Athena Diagnostics Inc
United States
1511
  • C Sequence analysis of the entire coding region

CMT Advanced Evaluation - Dominant

Athena Diagnostics Inc
United States
1813
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1103676
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Neuropathies NGS Panel

Fulgent Genetics
United States
9138
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 41 to 54 of 54

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.