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Results: 81 to 94 of 94

Tests names and labsConditionsGenes, analytes, and microbesMethods

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

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

Single gene testing SDHB

CeGaT GmbH
Germany
51
  • C Sequence analysis of the entire coding region

Single gene testing SDHD

CeGaT GmbH
Germany
41
  • C Sequence analysis of the entire coding region

Hereditary Paraganglioma-Pheochromocytoma Syndromes, SDHD sequencing

Molecular Diagnostics Laboratory Seoul National University Hospital
South Korea
11
  • D Deletion/duplication analysis
  • 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

SDHB Single Gene

Fulgent Genetics
United States
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SDHD Single Gene

Fulgent Genetics
United States
51
  • 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

Hereditary Gastrointestinal Cancer Panel, Sequencing and Deletion/Duplication

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
2226
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • 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

Leukoencephalopathy NGS Panel

Fulgent Genetics
United States
15569
  • D Deletion/duplication analysis
  • 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

SDHB-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome

Cancer Genomic Medicine Translational Research Lab Cleveland Clinic Genomic Medicine Institute
United States
21
  • D Deletion/duplication analysis
  • S Mutation scanning of the entire coding region
  • E Sequence analysis of select exons

Results: 81 to 94 of 94

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.