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Results: 1 to 20 of 20

Tests names and labsConditionsGenes, analytes, and microbesMethods

Sequencing of risk exons of the RET proto-oncogene (exons 8, 10, 11, 13, 14, 15, 16)

Department of Molecular Endocrinology Institute of Endocrinology
Czech Republic
51
  • E Sequence analysis of select exons

TMEM127 Gene Sequencing by Massively Parallel Sequencing (BCM-NGSSM)

Baylor Genetics
United States
11
  • E Sequence analysis of select exons

MAX Gene Sequencing by Massively Parallel Sequencing (BCM-NGSSM)

Baylor Genetics
United States
11
  • E Sequence analysis of select exons

SDHB Sequence Analysis (Prenatal Diagnosis)

Baylor Genetics
United States
11
  • E Sequence analysis of select exons

SDHD Sequence Analysis

Baylor Genetics
United States
11
  • E Sequence analysis of select exons

SDHD Sequence Analysis (Familial Mutation/Variant Analysis)

Baylor Genetics
United States
11
  • E Sequence analysis of select exons

MAX Sequence Analysis (Prenatal Sequence Analysis)

Baylor Genetics
United States
11
  • E Sequence analysis of select exons

Comprehensive Hereditary Cancer Panel

Baylor Genetics
United States
13261
  • E Sequence analysis of select exons

Hereditary Endocrine Cancer Panel

Baylor Genetics
United States
5115
  • E Sequence analysis of select exons

Hereditary Paraganglioma/Pheochromocytoma Panel

Baylor Genetics
United States
219
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons

Hereditary Renal Cancer Panel

Baylor Genetics
United States
4113
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons

Hereditary Cancer Panel, Sequencing and Deletion/Duplication

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
3373
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

MAX-Related Susceptibility to Pheochromocytoma

Exeter Molecular Genetics Laboratory
United Kingdom
11
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

RET-Related Pheochromocytoma

Exeter Molecular Genetics Laboratory
United Kingdom
11
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

SDHAF2-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome

Exeter Molecular Genetics Laboratory
United Kingdom
11
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

SDHB-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome

Exeter Molecular Genetics Laboratory
United Kingdom
11
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

SDHC-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome

Exeter Molecular Genetics Laboratory
United Kingdom
11
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

SDHD-Related Hereditary Paraganglioma-Pheochromocytoma Syndrome

Exeter Molecular Genetics Laboratory
United Kingdom
11
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

TMEM127-Related Susceptibility to Pheochromocytoma

Exeter Molecular Genetics Laboratory
United Kingdom
11
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

VHL-Related Pheochromocytoma

Exeter Molecular Genetics Laboratory
United Kingdom
11
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 20

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.