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Results: 121 to 138 of 138

Tests names and labsConditionsGenes, analytes, and microbesMethods

PARK2 Gene Sequencing and Deletion/Duplication Analysis

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

AKT1 Gene Sequencing and Deletion/Duplication Analysis

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PIK3CA Gene Sequencing and Deletion/Duplication Analysis

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
111
  • 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

Nephroblastoma

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

Single gene testing PANK2

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

Invitae Breast and Gyn Cancers Guidelines-Based Panel

Invitae
United States
2619
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Breast Cancer Panel

Invitae
United States
1914
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CLOVE syndrome, somatic (PIK3CA)

MVZ Dr. Eberhard & Partner Dortmund
Germany
101
  • E Sequence analysis of select exons

AKT1 Single Gene

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

PIK3CA Single Gene

Fulgent Genetics
United States
121
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CTNNB1 Single Gene

Fulgent Genetics
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CDH1 Single Gene

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

Invitae Breast and Gyn Cancers Panel

Invitae
United States
3323
  • 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

Comprehensive Eye Disorders NGS Panel

Fulgent Genetics
United States
1018459
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 121 to 138 of 138

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.