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Results: 21 to 40 of 45

Tests names and labsConditionsGenes, analytes, and microbesMethods

Childhood Epilepsy NGS Panel

Fulgent Genetics
United States
354209
  • 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

Erythromelalgia (SCN9A Single Gene Test)

Fulgent Genetics
United States
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Insensitivity To Pain (SCN9A Single Gene Test)

Fulgent Genetics
United States
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Paroxysmal Extreme Pain Disorder NGS Panel

Fulgent Genetics
United States
18553
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Dravet Syndrome NGS Panel

Fulgent Genetics
United States
2711
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SCN9A-Related Inherited Erythromelalgia: gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • C Sequence analysis of the entire coding region

FAMILIAL ERYTHROMELALGIA OR ERYTHERMALGIA

Laboratorio de Genetica Clinica SL
Spain
11
  • C Sequence analysis of the entire coding region

Epilepsy

Asper Biogene Asper Biogene LLC
Estonia
210204
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Epilepsy Comprehensive NGS Panel

Fulgent Genetics
United States
729398
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Erythermalgia, primary

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Single gene testing SCN9A

CeGaT GmbH
Germany
41
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth Disease

Asper Biogene Asper Biogene LLC
Estonia
8974
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SCN9A Single Gene

Fulgent Genetics
United States
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • 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

Epileptic encephalopathy panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
5332
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Hereditary Neuropathies NGS Panel

Fulgent Genetics
United States
9138
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Small fiber neuropathy

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

Erythermalgia

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

Results: 21 to 40 of 45

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.