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Results: 61 to 77 of 77

Tests names and labsConditionsGenes, analytes, and microbesMethods

Kabuki Syndrome Panel

Blueprint Genetics
Finland
17
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Syndromic Hearing Loss Panel

Blueprint Genetics
Finland
686
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nephrology Endocrinology and Electrolytes - panels

MGZ Medical Genetics Center
Germany
5117
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cystic Disease and Nephronopthisis panel

Clinical Genomics Laboratory Washington University in St. Louis
United States
1633
  • C Sequence analysis of the entire coding region

Hearing Loss Panel

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
1121
  • C Sequence analysis of the entire coding region

CAKUT

Hildebrandt Laboratory Boston Children's Hospital
United States
2204
  • C Sequence analysis of the entire coding region

Branchiootorenal Syndrome Panel

CeGaT GmbH
Germany
44
  • C Sequence analysis of the entire coding region

Renal Dysplasia, Renal Agenesia, CAKUT Panel

CeGaT GmbH
Germany
132
  • C Sequence analysis of the entire coding region

Syndromic Hearing Loss Panel

CeGaT GmbH
Germany
162
  • C Sequence analysis of the entire coding region

SIX5 Deletion/duplication analysis

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • D Deletion/duplication analysis

SIX5 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

SIX5 Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Branchiootorenal syndrome 2

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • C Sequence analysis of the entire coding region

Branchiootorenal syndrome 2

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Branchiootorenal Spectrum Disorder Panel

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
53
  • C Sequence analysis of the entire coding region

OtoSeq Hearing Loss Panel by next-generation sequencing (NGS)

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
3623
  • C Sequence analysis of the entire coding region

Results: 61 to 77 of 77

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.