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Results: 61 to 78 of 78

Tests names and labsConditionsGenes, analytes, and microbesMethods

Invitae Sarcoma Panel

Invitae
United States
2726
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Renal/Urinary Tract Cancers Panel

Invitae
United States
3724
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Multi-Cancer Panel

Invitae
United States
13880
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Hereditary Paraganglioma-Pheochromocytoma Panel

Invitae
United States
1010
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Gastric Cancer Panel

Invitae
United States
2818
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Common Hereditary Cancers Panel (Breast, Gyn, GI)

Invitae
United States
7542
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary pheochromocytoma-paraganglioma type 3

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Pheochromocytoma and Paraganglioma Panel

CeGaT GmbH
Germany
713
  • C Sequence analysis of the entire coding region

Cancer Predisposition

Asper Biogene Asper Biogene LLC
Estonia
13598
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SDHC Single Gene

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1103676
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SDHC-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome

MGZ Medical Genetics Center
Germany
11
  • C Sequence analysis of the entire coding region

Hereditary Paraganglioma

Genetics Laboratory University of Oklahoma Health Sciences Center
United States
11
  • C Sequence analysis of the entire coding region

Hereditary Phaeochromocytoma/Paraganglioma Syndromes (MAX, SDHAF2, SDHB, SDHC, SDHD, TMEM127, VHL)

Molecular Genetics Laboratory - Diagnostics Genetics LabPLUS - Auckland City Hospital
New Zealand
67
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Paragangliomas 3

Center for Human Genetics, Inc
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SDHC-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome

Cancer Genomic Medicine Translational Research Lab Cleveland Clinic Genomic Medicine Institute
United States
11
  • D Deletion/duplication analysis
  • S Mutation scanning of the entire coding region
  • E Sequence analysis of select exons

Hereditary Paraganglioma-Pheochromocytoma Syndrome

Cancer Genomic Medicine Translational Research Lab Cleveland Clinic Genomic Medicine Institute
United States
43
  • D Deletion/duplication analysis
  • S Mutation scanning of the entire coding region
  • E Sequence analysis of select exons

Results: 61 to 78 of 78

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.