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Results: 21 to 40 of 88

Tests names and labsConditionsGenes, analytes, and microbesMethods

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 SDHC Gene

PreventionGenetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

GIST [detection of somatic mutations: KIT (exons 8 - 11, 13, 17 and 18), PDGFRA (exons 12, 14 and 18), BRAF (V600), CBL (exons 8 and 9), SDHA (whole coding region), SDHB (whole coding region), SDHC (whole coding region) and SDHD (whole coding region)]

CGC Genetics Unilabs
Portugal
38
  • E Sequence analysis of select exons

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

SDHC

Institute of Human Genetics Medical University Innsbruck
Austria
31
  • 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

Hereditary Paraganglioma-Pheochromocytoma

Genologica Medica
Spain
3212
  • C Sequence analysis of the entire coding region

Renal cancer

Asper Biogene Asper Biogene LLC
Estonia
4825
  • C Sequence analysis of the entire coding region

Mitochondrial genome sequencing

Molecular Vision Laboratory
United States
526339
  • C Sequence analysis of the entire coding region

VistaSeq Comprehensive Cancer Panel

Molecular Diagnostic Laboratory LabCorp
United States
4759
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SDHC Full Gene Sequencing Analysis

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
31
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 88

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.