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Results: 21 to 40 of 97

Tests names and labsConditionsGenes, analytes, and microbesMethods

Variant Resolution Test for CancerNext-Expanded® (+RNAinsight®)

Ambry Genetics
United States
14118
  • D Deletion/duplication analysis
  • R RNA analysis
  • C Sequence analysis of the entire coding region

SDHB - hereditary paraganglioma and pheochromocytoma

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
21
  • C Sequence analysis of the entire coding region

Pediatric Cancer Panel

PreventionGenetics
United States
7864
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Leukodystrophy and Leukoencephalopathy Panel

PreventionGenetics
United States
201211
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

RenalNext®

Ambry Genetics
United States
5720
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PGLNext®

Ambry Genetics
United States
2614
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CustomNext-Cancer®

Ambry Genetics
United States
14791
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CancerNext-Expanded®

Ambry Genetics
United States
14177
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Pheochromocytoma and Paraganglioma Panel

Genetic Services Laboratory University of Chicago
United States
1016
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cancer Panel

PreventionGenetics
United States
122117
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Renal Cancer Panel

PreventionGenetics
United States
3325
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hereditary Paraganglioma-Pheochromocytoma (PGL/PCC) Syndrome Panel

PreventionGenetics
United States
1313
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

MitoMet®Plus aCGH Analysis

Baylor Genetics
United States
842637
  • D Deletion/duplication analysis

Hereditary Paraganglioma-Pheochromocytoma Syndrome via the SDHB Gene

PreventionGenetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hereditary Paraganglioma-Pheochromocytoma Expanded Panel, Sequencing and Deletion/Duplication

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
1212
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SDHB

Division of Human Genetics Medical University Innsbruck
Austria
51
  • S Mutation scanning of the entire coding region
  • C Sequence analysis of the entire coding region

Inherited Cancer Panel

Dhiti Omics Technologies Private Ltd
India
13684
  • C Sequence analysis of the entire coding region

Hereditary pediatric cancer panel. NGS panel of 71 genes.

Genologica Medica
Spain
15871
  • C Sequence analysis of the entire coding region

Hereditary endocrine cancer panel. NGS panel of 22 genes.

Genologica Medica
Spain
6822
  • C Sequence analysis of the entire coding region

Hereditary kidney cancer panel. NGS panel of 26 genes.

Genologica Medica
Spain
7426
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 97

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.