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Results: 1 to 14 of 14

Tests names and labsConditionsGenes, analytes, and microbesMethods

SUFU Sequence Analysis (Familial Mutation/Variant Analysis)

Baylor Genetics
United States
11
  • T Targeted variant analysis

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

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

Hereditary Colorectal/Gastrointestinal Cancer Panel

Baylor Genetics
United States
5822
  • E Sequence analysis of select exons

Comprehensive Hereditary Cancer Panel

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

Hereditary Leukemia/Lymphoma Panel

Baylor Genetics
United States
3613
  • E Sequence analysis of select exons

Hereditary Pancreatic Cancer Panel

Baylor Genetics
United States
4617
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons

Hereditary Prostate Cancer Panel

Baylor Genetics
United States
245
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons

Hereditary Melanoma Panel

Baylor Genetics
United States
214
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons

Hereditary High Risk Breast Cancer Panel

Baylor Genetics
United States
357
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

BRCA1 & BRCA2 Seq and Del/Dup Analysis

Baylor Genetics
United States
102
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Brain, CNS, PNS Cancer Panel

Baylor Genetics
United States
4317
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary High Risk Breast Cancer Panel

Baylor Genetics
United States
347
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Brain, CNS, PNS Cancer Panel

Baylor Genetics
United States
4317
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

BRCA1 & BRCA2 Seq and Del/Dup Analysis

Baylor Genetics
United States
102
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 14 of 14

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.