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Results: 21 to 40 of 75

Tests names and labsConditionsGenes, analytes, and microbesMethods

Familial Hemiplegic Migraine 1 (FHM1) via the CACNA1A Gene

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

Early Infantile Epileptic Encephalopathy Panel

PreventionGenetics, Part of Exact Sciences
United States
144124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

CACNA1A

Institute for Human Genetics University Medical Center Freiburg
Germany
41
  • C Sequence analysis of the entire coding region

Hereditary ataxias. NGS panel of 139 genes.

Genologica Medica
Spain
220139
  • C Sequence analysis of the entire coding region

Ataxia panel. NGS panel of 157 genes.

Genologica Medica
Spain
247156
  • C Sequence analysis of the entire coding region

Epileptic encephalopathy panel. 128-gene NGS panel.

Genologica Medica
Spain
197128
  • C Sequence analysis of the entire coding region

Migraine panel. NGS panel of 10 genes.

Genologica Medica
Spain
3010
  • C Sequence analysis of the entire coding region

Complete epilepsy panel. NGS panel of 283 genes.

Genologica Medica
Spain
409283
  • C Sequence analysis of the entire coding region

CACNA1A Copy Number Analysis

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
31
  • D Deletion/duplication analysis

CACNA1A Full Gene Sequencing Analysis

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
31
  • C Sequence analysis of the entire coding region

Familial Hemiplegic Migraine (NGS Panel and Copy Number Analysis + mtDNA)

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
46
  • C Sequence analysis of the entire coding region

Familial Hemiplegic Migraine

Asper Biogene Asper Biogene LLC
Estonia
2813
  • C Sequence analysis of the entire coding region

Hemiplegic Migraine Panel

GeneDx
United States
114
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Childhood Epilepsy NGS Panel

Fulgent Genetics
United States
354209
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

GABA Metabolism Deficiency NGS Panel

Fulgent Genetics
United States
2430
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neonatal Epilepsy NGS Panel

Fulgent Genetics
United States
509275
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Adolescent/Adult Epilepsy NGS Panel

Fulgent Genetics
United States
18282
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neurotransmitter Metabolism Deficiency NGS Panel

Fulgent Genetics
United States
85101
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nondystrophic Myotonia NGS Panel

Fulgent Genetics
United States
3510
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Late-Onset Ataxia NGS Panel

Fulgent Genetics
United States
13356
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 75

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