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Results: 61 to 80 of 84

Tests names and labsConditionsGenes, analytes, and microbesMethods

Beacon Expanded Male Carrier Screening Panel

Fulgent Genetics
United States
636298
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Male Carrier Screening Plus Panel

Fulgent Genetics
United States
661306
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Ashkenazi Jewish Male Carrier Screening Panel

Fulgent Genetics
United States
14541
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Female Carrier Screening Panel

Fulgent Genetics
United States
690326
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

USHER SYNDROME TYPE 1

Laboratorio de Genetica Clinica SL
Spain
55
  • C Sequence analysis of the entire coding region

Usher Syndrome, Types 1F and 3 (PCDH15 and CLRN1), 2 Variants

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
22
  • T Targeted variant analysis

Ashkenazi Jewish Panel

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

USHER syndrome panel

Molecular Vision Laboratory
United States
2414
  • 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

Usher Syndrome Panel

CeGaT GmbH
Germany
1715
  • C Sequence analysis of the entire coding region

PCDH15 Deletion/duplication analysis

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
21
  • D Deletion/duplication analysis

PCDH15 Single Gene

Fulgent Genetics
United States
31
  • 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

Usher Syndrome NGS Panel

Fulgent Genetics
United States
2112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PCDH15 Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
31
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Retinitis Pigmentosa NGS Panel

Fulgent Genetics
United States
329124
  • 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

Ciliopathies NGS Panel

Fulgent Genetics
United States
14197
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ashkenazi Jewish Diseases, 16 Genes

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
1716
  • T Targeted variant analysis

Results: 61 to 80 of 84

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.