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Results: 101 to 120 of 120

Tests names and labsConditionsGenes, analytes, and microbesMethods

Inherited Cancer Panel

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
3349
  • 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

Overgrowth/Macrocephaly NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
1616
  • C Sequence analysis of the entire coding region

PTCH1 Gene Sequencing and Deletion/Duplication Analysis

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hemato-oncology chromosomal microarray

Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center
United States
2393
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Gorlin syndrome

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

Single gene testing PTCH1

CeGaT GmbH
Germany
31
  • C Sequence analysis of the entire coding region

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

Cancer Predisposition

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

PTCH1 Single Gene

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

PTCH2 Single Gene

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

SUFU Single Gene

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

Holoprosencephaly NGS Panel

Fulgent Genetics
United States
137
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Basal Cell Nevus Syndrome Panel

Invitae
United States
22
  • 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

Basal Cell Nevus Syndrome

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Basal Cell Nevus Syndrome

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Nevoid Basal Cell Carcinoma Syndrome

MGZ Medical Genetics Center
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary onco-endocrino tumors (50 genes)

Center for Human Genetics Cliniques Universitaires Saint Luc
Belgium
2549
  • C Sequence analysis of the entire coding region

Breast and Ovarian Cancer

Asper Biogene Asper Biogene LLC
Estonia
1523
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 101 to 120 of 120

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.