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Results: 1 to 16 of 16 (representing 14 labs)

Tests names and labsConditionsGenes and analytesMethods

ATP2A2. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

X-chromosome High Resolution microarray analysis

Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center
United States
242171
  • D Deletion/duplication analysis

Darier-White Disease, Sequencing ATP2A2 Gene

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

DARIER-WHITE DISEASE

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

ATP2A2

Institute for Human Genetics University Clinic Freiburg
Germany
21
  • 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

Darier disease

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

Single gene testing ATP2A2

CeGaT GmbH
Germany
21
  • C Sequence analysis of the entire coding region

Darier disease (sequence analysis of ATP2A2 gene)

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

ATP2A2 Gene Sequencing

GeneDx
United States
11
  • S Mutation scanning of the entire coding region

ATP2A2

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

Epilepsy Advanced Sequencing Evaluation - Syndromic Disorders

Athena Diagnostics Inc
United States
2626
  • C Sequence analysis of the entire coding region

Epilepsy Advanced Sequencing Evaluation

Athena Diagnostics Inc
United States
143141
  • 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

Darier-White disease: ATP2A2 gene sequence analysis

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
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 16 of 16

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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