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Results: 1 to 20 of 22 (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

nucSEEKĀ® Comprehensive Sequence Analysis Of The Nuclear Mitochondrial Exome

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
560420
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

JUVENILE MYOCLONIC EPILEPSY

Laboratorio de Genetica Clinica SL
Spain
44
  • C Sequence analysis of the entire coding region

CLCN2 Single Gene Test

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
21
  • D Deletion/duplication analysis
  • 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

Myoclonic Seizures B Spotlight Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
3618
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Epilepsy NGS Panel

Fulgent Genetics
United States
3052447
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Idiopathic Generalized Epilepsy NGS Panel

Fulgent Genetics
United States
106789
  • 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

Epilepsy, idiopathic generalized type 11 (sequence analysis of CLCN2 gene)

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

Hereditary Spastic Paraplegias (HSP) and differential diagnoses Panel

CeGaT GmbH
Germany
147143
  • C Sequence analysis of the entire coding region

CLCN2

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

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
601504
  • D Deletion/duplication 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

Febrile seizures / genetic epilepsy with febrile seizures plus (GEFS+) panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
2210
  • 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, juvenile myoclonic 8

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Epilepsy, idiopathic generalized, 11

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Epilepsy, juvenile myoclonic 8

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 22

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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