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Results: 101 to 116 of 116

Tests names and labsConditionsGenes, analytes, and microbesMethods

Invitae Peutz-Jeghers Syndrome Test

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

Invitae Familial Adenomatous Polyposis Test

Invitae
United States
81
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Lynch Syndrome Panel

Invitae
United States
95
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

BRAF Single Gene

Fulgent Genetics
United States
71
  • D Deletion/duplication analysis
  • 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

Intellectual Disability NGS Panel

Fulgent Genetics
United States
1058554
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Autism NGS Panel

Fulgent Genetics
United States
170106
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MSH6 Sequencing and Deletion/Duplication

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MSH6 Deletion/Duplication

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
31
  • D Deletion/duplication analysis

MSH2 Sequencing and Deletion/Duplication

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MSH2 Deletion/Duplication

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
41
  • D Deletion/duplication analysis

MLH1 Sequencing and Deletion/Duplication

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MLH1 Deletion/Duplication

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
41
  • D Deletion/duplication analysis

Comprehensive Cardiovascular NGS Panel

Fulgent Genetics
United States
671250
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Lynch syndrome/HNPCC (MLH1, MSH2, MSH6, PMS2, TACSTD1)

Center for Human Genetics, Inc
United States
25
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 101 to 116 of 116

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.