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Results: 101 to 120 of 120

Tests names and labsConditionsGenes, analytes, and microbesMethods

Retinitis Pigmentosa NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
10392
  • C Sequence analysis of the entire coding region

GeneAware™ Ashkenazi Jewish Panel (Male)

Baylor Genetics
United States
137
  • C Sequence analysis of the entire coding region

GeneAware™ Ashkenazi Jewish Panel (Female)

Baylor Genetics
United States
139
  • C Sequence analysis of the entire coding region

GeneAware™ Complete Panel (Male)

Baylor Genetics
United States
1146
  • C Sequence analysis of the entire coding region

GeneAware™ Complete Panel (Female)

Baylor Genetics
United States
1156
  • C Sequence analysis of the entire coding region

DHDDS single gene sequencing

Molecular Vision Laboratory
United States
11
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Retinal Dystrophy Panel

Blueprint Genetics
Finland
1260
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Metabolism Panel

Blueprint Genetics
Finland
14434
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Retinitis Pigmentosa Panel

Blueprint Genetics
Finland
1110
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Disorders of Glycosylation Panel

Blueprint Genetics
Finland
147
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ashkenazi Jewish Panel

Molecular Vision Laboratory
United States
128
  • C Sequence analysis of the entire coding region

Retinal Dystrophy Panel

Molecular Vision Laboratory
United States
379287
  • C Sequence analysis of the entire coding region

Retinitis pigmentosa, autosomal recessive and X-linked Panel

CeGaT GmbH
Germany
3762
  • C Sequence analysis of the entire coding region

Congenital Disorders of Glycosylation (CDG)

MGZ Medical Genetics Center
Germany
438
  • C Sequence analysis of the entire coding region

DHDDS Single Gene

Fulgent Genetics
United States
11
  • 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

Retinitis Pigmentosa NGS Panel

Fulgent Genetics
United States
329124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Disorders of Glycosylation NGS Panel

Fulgent Genetics
United States
4339
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MitoMet®Plus aCGH Analysis

Baylor Genetics
United States
842637
  • D Deletion/duplication analysis

Comprehensive Eye Disorders NGS Panel

Fulgent Genetics
United States
1018459
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 101 to 120 of 120

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.