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Results: 1 to 15 of 15

Tests names and labsConditionsGenes and analytesMethods

Ataxia Exome Panel

Genetic Services Laboratory University of Chicago
United States
287480
  • 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

Invitae Alternating Hemiplegia of Childhood Panel

Invitae
United States
72
  • 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

Familial Migraine and Epilepsy (CACNA1A) Targeted Testing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
11
  • T Targeted variant analysis

Migraine and Strokes Panel

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

Comprehensive Epilepsy NGS Panel

Fulgent Genetics
United States
3032447
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Early-Onset Epileptic Encephalopathy NGS Panel

Fulgent Genetics
United States
1005133
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Idiopathic Generalized Epilepsy NGS Panel

Fulgent Genetics
United States
106589
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Essential Epilepsy NGS Panel

Fulgent Genetics
United States
79370
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Migraine Panel

CeGaT GmbH
Germany
510
  • C Sequence analysis of the entire coding region

Familial hemiplegic migraine, episodic ataxia type 2, CACNA1A sequencing

Molecular Diagnostics Laboratory Seoul National University Hospital
South Korea
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Familial Hemiplegic Migraine

Medizinisch Genetisches Zentrum München MGZ München
Germany
15
  • C Sequence analysis of the entire coding region

Familial hemiplegic migraine type 2 (FHM2, deletion/duplication analysis of ATP1A2 gene)

CGC Genetics
Portugal
21
  • D Deletion/duplication analysis

Autism/Intellectual Disability/Multiple Anomalies

Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center
United States
11389
  • C Sequence analysis of the entire coding region

Results: 1 to 15 of 15

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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