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Results: 1 to 20 of 61 (representing 26 labs)

Tests names and labsConditionsGenes and analytesMethods

Hereditary Pheochromocytoma and Paraganglioma Panel

Genetic Services Laboratory University of Chicago
United States
1014
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SDHD, SDHB, SDHC. MLPA testing

Instituto de Medicina Genomica
Spain
43
  • D Deletion/duplication analysis

SDHC. Complete sequencing

Instituto de Medicina Genomica
Spain
21
  • C Sequence analysis of the entire coding region

SDHB, SDHD, SDHC. Complete sequencing

Instituto de Medicina Genomica
Spain
43
  • C Sequence analysis of the entire coding region

Renal Cancer Sequencing Panel

PreventionGenetics
United States
2619
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hereditary Paraganglioma-Pheochromocytoma Syndrome Sequencing Panel

PreventionGenetics
United States
1212
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

MitoMet®Plus aCGH Analysis

Baylor Miraca Genetics Laboratories Baylor College of Medicine
United States
845637
  • 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

nucSEEK® Comprehensive Sequence Analysis Of The Nuclear Mitochondrial Exome

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
560420
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Paraganglioma-Pheochromocytoma (SDHC) Sequencing and Deletion/Duplication

ARUP Laboratories, Molecular Genetics and Genomics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PHEOCHROMOCYTOMA-PARAGANGLIOMA

Laboratorio de Genetica Clinica SL
Spain
69
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pheochromocytoma and paraganglioma (NGS panel for 16 genes)

CGC Genetics
Portugal
1016
  • C Sequence analysis of the entire coding region

Pheochromocytoma and paraganglioma (NGS panel for 16 genes)

CGC Genetics
Portugal
1016
  • C Sequence analysis of the entire coding region

Hereditary Pheochromocytoma-Paraganglioma Syndrome, Deletions-Duplications (MLPA) SDHC Gene

Reference Laboratory Genetics
Spain
11
  • D Deletion/duplication analysis

Hereditary Pheochromocytoma-Paraganglioma Syndrome Type 3, Sequencing SDHC/PGL3Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Comprehensive Hereditary Cancer Panel

Baylor Miraca Genetics Laboratories Baylor College of Medicine
United States
13561
  • E Sequence analysis of select exons

Hereditary Endocrine Cancer Panel

Baylor Miraca Genetics Laboratories Baylor College of Medicine
United States
5415
  • E Sequence analysis of select exons

Hereditary Paraganglioma/Pheochromocytoma Panel

Baylor Miraca Genetics Laboratories Baylor College of Medicine
United States
229
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons

Hereditary Renal Cancer Panel

Baylor Miraca Genetics Laboratories Baylor College of Medicine
United States
4413
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons

Invitae Pediatric Solid Tumors Panel

Invitae
United States
9148
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 61

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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