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Results: 121 to 140 of 151

Tests names and labsConditionsGenes, analytes, and microbesMethods

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

GeneAware™ ACMG & ACOG Panel (Female)

Baylor Genetics
United States
125
  • 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™ ACMG & ACOG Panel (Male)

Baylor Genetics
United States
123
  • 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

Maple syrup urine disease, type Ib (BCKDHB)

Amsterdam UMC, Location AMC Laboratory Genetic Metabolic Diseases, LGMD
Netherlands
11
  • A Analyte
  • C Sequence analysis of the entire coding region

Organic Acidemia/Aciduria & Cobalamin Deficiency Panel

Blueprint Genetics
Finland
653
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hyperammonemia and Urea Cycle Disorder Panel

Blueprint Genetics
Finland
248
  • 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

Neurogenetic Disorders - panels

MGZ Medical Genetics Center
Germany
14597
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Maple Syrup Urine Disease, Type 1B (BCKDHB), 3 Variants

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
11
  • T Targeted variant analysis

Ashkenazi Jewish Carrier Screening Panel

Center for Human Genetics, Inc
United States
118
  • T Targeted variant analysis

Maple syrup urine disease

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

Single gene testing BCKDHB

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Nuclear encoded Mitochondriopathies Panel

CeGaT GmbH
Germany
37284
  • C Sequence analysis of the entire coding region

BCKDHB

Institute of Human Genetics Medical University Innsbruck
Austria
11
  • S Mutation scanning of the entire coding region

Results: 121 to 140 of 151

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.