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Results: 1 to 20 of 60

Tests names and labsConditionsGenes and analytesMethods

Rapid microarray (CGH and SNP)

Allele Diagnostics
United States
247231
  • H Detection of homozygosity
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Paragangliomas type 4

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

SDHB-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome

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

SDHB-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome

(AC) Atlanta Center: Medical Neurogenetics, LLC.
United States
11
  • C Sequence analysis of the entire coding region

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

SDHB. 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 NextGen Sequencing (NGS) 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
United States
845637
  • 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

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 (SDHB) Sequencing and Deletion/Duplication

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

Invitae Pediatric Solid Tumors Panel

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

Comprehensive Hereditary Cancer Panel

Genetic Services Laboratory University of Chicago
United States
1750
  • C Sequence analysis of the entire coding region

PARAGANGLIOMA-PHEOCHROMOCYTOMA

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
1011
  • C Sequence analysis of the entire coding region

Invitae Sarcoma Panel

Invitae
United States
2730
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Renal/Urinary Tract Cancers Panel

Invitae
United States
3829
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Paraganglioma-Pheochromocytoma Panel

Invitae
United States
1814
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 60

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.