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Results: 1 to 20 of 125

Tests names and labsConditionsGenes and analytesMethods

New Born testing (CentoICU)

Centogene AG - the Rare Disease Company
Germany
767514
  • C Sequence analysis of the entire coding region

CentoICU platinum plus

Centogene AG - the Rare Disease Company
Germany
768514
  • C Sequence analysis of the entire coding region

AllNeuro panel

Centogene AG - the Rare Disease Company
Germany
7861205
  • C Sequence analysis of the entire coding region

Baby Genes Targeted Panel

Baby Genes Inc.
United States
8990
  • T Targeted variant analysis

Methylenetetrahydrofolate Reductase Deficiency

Clinical Molecular Genetics Laboratory Johns Hopkins All Children's Hospital
United States
41
  • S Mutation scanning of the entire coding region
  • E Sequence analysis of select exons

Tempus xT assay

Tempus Labs, Inc.
United States
2594
  • I Microsatellite instability testing (MSI)
  • R RNA analysis
  • C Sequence analysis of the entire coding region

Genecept Assay™

Genomind Genomind, Inc
United States
1318
  • D Deletion/duplication analysis
  • T Targeted variant analysis

Expanded Comprehensive Medication Metabolism

Molecular Diagnostics and Toxicology Laboratory
United States
77
  • T Targeted variant analysis

Comprehensive Medication Metabolism

Molecular Diagnostics and Toxicology Laboratory
United States
77
  • T Targeted variant analysis

Cardiac Medication Metabolism

Molecular Diagnostics and Toxicology Laboratory
United States
77
  • T Targeted variant analysis

MTHFR

Genelex
United States
41
  • T Targeted variant analysis

Homocystinuria

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Genetic Study of Hereditary Thrombophilia (11 genes)

HeartGenetics, Genetics and Biotechnology, SA
Portugal
110
  • E Sequence analysis of select exons
  • T Targeted variant analysis

MTHFR Sequence Analysis

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
11
  • C Sequence analysis of the entire coding region

CEN4GEN rapid supplemental newborn genetic screen: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
199
  • C Sequence analysis of the entire coding region

CEN4GEN rapid pan-ethnic carrier screen: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
1104
  • C Sequence analysis of the entire coding region

MTHFR A1298C C677T

IBC Instituto de Bioquimica Clinica SRL
Argentina
11
  • T Targeted variant analysis

152 Integrated Advantage NGS Solid Tumor Panel

Integrated Molecular Diagnostics Pathology, Inc.
United States
6152
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Disorders Related to Metabolism of Cobalamin, Folate and Homocysteine Sequencing Panel with CNV Detection

PreventionGenetics
United States
2831
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Rxight Pharmacogenetics Program

MD Labs
United States
7920
  • A Analyte

Results: 1 to 20 of 125

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.

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