Filters

See more specimen types...
See more states

Other countries

See more countries

Results: 1 to 20 of 61 (representing 27 labs)

Tests names and labsConditionsGenes and analytesMethods

Familial hemiplegic migraine

Ambry Genetics
United States
44
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

AllNeuro panel

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

Familial hemiplegic migraine type 2

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

Dystonia Exome Panel

Genetic Services Laboratory University of Chicago
United States
93170
  • C Sequence analysis of the entire coding region

Next Generation Sequencing for FHM, EA2, SCA6, CADASIL, Epilepsy

Genomics Research Centre Diagnostics Clinic Queensland Unstitute of Technology
Australia
94
  • C Sequence analysis of the entire coding region

Epilepsy Panel - Comprehensive

Molecular Genetics Laboratory London Health Sciences Centre
Canada
6969
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Familial Hemiplegic Migraine Sequencing Panel

PreventionGenetics
United States
44
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Familial Hemiplegic Migraine 2 (FHM2) via the ATP1A2 Gene

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

ATP1A2, CACNA1A, SCN1A. NextGeneDx.Complete sequencing by NGS

Instituto de Medicina Genomica
Spain
33
  • C Sequence analysis of the entire coding region

ATP1A2. Complete sequencing

Instituto de Medicina Genomica
Spain
21
  • C Sequence analysis of the entire coding region

ATP1A2. Complete sequencing

Instituto de Medicina Genomica
Spain
21
  • C Sequence analysis of the entire coding region

Familial hemiplegic migraine type 2

LifeLabs Genetics
Canada
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Migraine Spotlight Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
3312
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Migraine Panel

Blueprint Genetics
Finland
210
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neurogenetic Disorders - panels

Medizinisch Genetisches Zentrum München MGZ München
Germany
14597
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Movement Disorders Panel

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health and Science University
United States
492
  • C Sequence analysis of the entire coding region

Migraine and Strokes Panel

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health and Science University
United States
38
  • C Sequence analysis of the entire coding region

Epilepsy/Seizure

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health and Science University
United States
598
  • C Sequence analysis of the entire coding region

Dystonia

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health and Science University
United States
477
  • C Sequence analysis of the entire coding region

Invitae Epilepsy Panel

Invitae
United States
111103
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 61

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.

Support Center