Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Hereditary Sensory and Autonomic Neuropathy Panel PreventionGenetics, part of Exact Sciences United States | 20 | 20 |
|
Charcot-Marie-Tooth - Axonal Neuropathy Panel PreventionGenetics, part of Exact Sciences United States | 46 | 37 |
|
Charcot-Marie-Tooth (CMT) - Comprehensive Panel PreventionGenetics, part of Exact Sciences United States | 91 | 83 |
|
Hereditary Motor and Sensory Neuropathy IIB (HMSN2B) via the RAB7A Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
Invitae Charcot-Marie Tooth Disease Comprehensive Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 123 | 52 |
|
GeneSeq® Neuro: Charcot-Marie-Tooth Disease Panel MNG Laboratories (Medical Neurogenetics, LLC.) United States | 1 | 98 |
|
GeneSeq® Neuro: Hereditary Sensory and Autonomic Neuropathy Panel MNG Laboratories (Medical Neurogenetics, LLC.) United States | 1 | 24 |
|
Institute for Human Genetics University Medical Center Freiburg Germany | 1 | 1 |
|
Charcot-Marie-Tooth disease (WES based NGS panel of 43 genes, including analysis of CNVs) CGC Genetics Unilabs Portugal | 1 | 43 |
|
Charcot-Marie-Tooth disease type 2B (CMT2B, sequence analysis of RAB7A gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Mendelics Brazil | 1 | 104 |
|
HEREDITARY SENSORY-AUTONOMIC NEUROPATHY EXOME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 30 |
|
CHARCOT-MARIE-TOOTH EXOME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 151 |
|
Codex Genetics Limited Hong Kong | 1 | 490 |
|
Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
|
Xpanded Adult Movement Disorders Panel GeneDx United States | 5 | 473 |
|
Prenatal Known Familial Mutation GeneDx United States | 1 | 1716 |
|
Custom XomeDxSlice (2-150 Genes, Proband Only) GeneDx United States | 1 | 1718 |
|
GeneDx United States | 1 | 1040 |
|
Two Known Familial Variants in a Nuclear Gene GeneDx United States | 1 | 1043 |
|
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.