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Results: 21 to 32 of 32

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hearing Loss Advanced Sequencing and CNV Evaluation

Athena Diagnostics
United States
249181
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

WAARDENBURG SYNDROME TYPE 2

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

Waardenburg Syndrome Panel 

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
96
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Waardenburg Syndrome panel

Molecular Vision Laboratory
United States
197
  • C Sequence analysis of the entire coding region

Hearing Loss NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
198157
  • C Sequence analysis of the entire coding region

Waardenburg Syndrome

Asper Biogene Asper Biogene LLC
Estonia
97
  • C Sequence analysis of the entire coding region

Genetic disorders with abnormal pigmentation Panel

CeGaT GmbH
Germany
2932
  • C Sequence analysis of the entire coding region

Hermansky-Pudlak Syndrome/Oculocutaneous Albinism/Pigmentation panel

Molecular Vision Laboratory
United States
4529
  • C Sequence analysis of the entire coding region

SNAI2 Single Gene

Fulgent Genetics
United States
21
  • 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

Waardenburg Syndrome NGS Panel

Fulgent Genetics
United States
196
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Albinism NGS Panel

Fulgent Genetics
United States
5228
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 32 of 32

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.