Filters

See more specimen types...

Other countries

Results: 1 to 20 of 34

Tests names and labsConditionsGenes and analytesMethods

GABRG2

Amplexa Genetics Amplexa Genetics A/S
Denmark
11
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

EpiFirst - Fever

Ambry Genetics
United States
2013
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Generalized Epilepsy With Febrile Seizures Plus via the GABRG2 Gene

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

Epilepsy: Generalized Epilepsy with Febrile Seizures Plus (GEFS+) NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
55
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Early Infantile Epileptic Encephalopathy NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
6664
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

SCN1A, SCN1B, GABRG2, GABRD, SCN9A. NextGeneDx.Complete sequencing by NGS

Instituto de Medicina Genomica
Spain
55
  • C Sequence analysis of the entire coding region

MECP2, SCN1B, GABRG2, LGI1, POLG, POLG2, SLC25A22, SPTAN1, SRPX2. NextGeneDx.Complete sequencing by NGS

Instituto de Medicina Genomica
Spain
209
  • C Sequence analysis of the entire coding region

Early Infantile Epileptic Encephalopathy, Dominant and X-linked NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
2624
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Epilepsy Panel

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

EPILEPSY HEREDITARY PANEL

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
4137
  • C Sequence analysis of the entire coding region

DRAVET, SYNDROME & MIOCLONIC EPILEPSY

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
1713
  • C Sequence analysis of the entire coding region

EpilepsyNext

Ambry Genetics
United States
104100
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Epileptic encephalopathy (NGS panel for 67 genes)

CGC Genetics
Portugal
6367
  • C Sequence analysis of the entire coding region

Single gene testing GABRG2

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Epilepsy, generalized, with febrile seizures plus (sequence analysis of GABRG2 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

Idiopathic Generalized and Focal Epilepsy Panel

CeGaT GmbH
Germany
2140
  • C Sequence analysis of the entire coding region

Febrile Seizures familial 8, GABRG2

MVZ Dortmund Dr. Eberhard and Partner
Germany
11
  • C Sequence analysis of the entire coding region

Febrile Seizures familial 8, GABRG2

MVZ Dortmund Dr. Eberhard and Partner
Germany
11
  • C Sequence analysis of the entire coding region

GABRG2

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

Epilepsy Advanced Sequencing Evaluation

Athena Diagnostics Inc Quest Diagnostics
United States
143141
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 34

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.