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Results: 1 to 20 of 48

Tests names and labsConditionsGenes and analytesMethods

SDHC-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome

(AC) Atlanta Center: Medical Neurogenetics, LLC.
United States
21
  • C Sequence analysis of the entire coding region

Hereditary Gastric Cancer Panel

Genetic Services Laboratory University of Chicago
United States
1019
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

TruGenome Predisposition Screen (Whole Genome Sequencing)

Illumina Clinical Services Laboratory Illumina
United States
15411578
  • 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

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

SDHD. Complete sequencing

Instituto de Medicina Genomica
Spain
21
  • 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 SDHD Gene

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

Renal / Urinary Cancer Comprehensive Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
77327
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Paraganglioma-Pheochromocytoma Comprehensive Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
37111
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Sarcoma Comprehensive Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
92126
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cancer Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
1736124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Renal / Urinary Cancer Comprehensive Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
77327
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Mitochondrial respiratory chain complex II, III, and IV deficiency

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
1921
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 48

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.