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Results: 1 to 15 of 15 (representing 11 labs)

Tests names and labsConditionsGenes and analytesMethods

AllNeuro panel

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

Childhood Absence Epilepsy , Sequencing CACNA1H Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Absence Seizures Spotlight Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
2010
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Benign Epilepsies Spotlight Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
2415
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Epilepsy

Asper Biotech Asper Biotech Ltd.
Estonia
121123
  • C Sequence analysis of the entire coding region

Autism

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
2528
  • 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

Epilepsy, childhood absence type 6 (sequence analysis of CACNA1H 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

CACNA1H

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

devACT® Next Generation Sequencing panel focused on genes that inform actionable clinical management of patients with Developmental Delay, Intellectual Disability, and Autism Spectrum Disorders

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
297248
  • L Linkage analysis
  • C Sequence analysis of the entire coding region

IGE/JME/CAE panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
2011
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Epilepsy NGS Panel

Fulgent Genetics
United States
597343
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Epilepsy, Childhood Absence, Susceptibility to, 6

Medizinisch Genetisches Zentrum München MGZ München
Germany
11
  • C Sequence analysis of the entire coding region

epiSEEK® Comprehensive Sequence Analysis for Epilepsy and Seizure Disorders

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
630431
  • D Deletion/duplication analysis
  • 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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