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Results: 21 to 40 of 811

Tests names and labsConditionsGenes, analytes, and microbesMethods

Whole Genome Sequencing for Hereditary Disorders, WGSDX

Mayo Clinic Laboratories Mayo Clinic
United States
11
  • C Sequence analysis of the entire coding region

Chromosome Analysis,Chorionic Villus w/rfl to Clarisure(R),Oligo-SNP,Prentl

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
31
  • K Karyotyping
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Chromosome Analysis,Amniotic Fluid w/rfl to Clarisure(R)Oligo-SNP,Prenatal

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
31
  • K Karyotyping
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Molecular Microscope Diagnostic System Heart

Kashi Clinical Laboratories
United States
11
  • R RNA analysis

Molecular Microscope Diagnostic System Kidney

Kashi Clinical Laboratories
United States
11
  • R RNA analysis

PGmax™ - Comprehensive Inherited Metabolic Disorders and Mitochondrial Disorders (Nuclear Genes only) Panel

PreventionGenetics, part of Exact Sciences
United States
101
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Transplant Rejection Allograft Check (TRAC™) donor-derived cell-free DNA (dd-cfDNA) assay

Transplant Genomics Inc.
United States
11
  • R RNA analysis

TruGraf Kidney Blood Gene Expression Test

Transplant Genomics Inc.
United States
11
  • X Protein expression

IriSight™ for Pregnancy Loss

Variantyx, Inc.
United States
32
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Epilepsy and Seizure Panel

PreventionGenetics, part of Exact Sciences
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

PGmax™ - Comprehensive Epilepsy and Seizure Panel

PreventionGenetics, part of Exact Sciences
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

PGmax™ - Comprehensive Movement Disorders Panel

PreventionGenetics, part of Exact Sciences
United States
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Percepta Genomic Sequencing Classifier

Veracyte, Inc.
United States
11
  • C Sequence analysis of the entire coding region

SNP Microarray Analysis (Chromosomal Microarray)

Institute for Genomic Medicine (IGM) Clinical Laboratory Nationwide Children's Hospital
United States
4521
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Familial Variant Targeted Sequencing

Institute for Genomic Medicine (IGM) Clinical Laboratory Nationwide Children's Hospital
United States
11
  • T Targeted variant analysis

Signatera

Natera, Inc.
United States
11
  • E Sequence analysis of select exons

5-Cell Confirmation Chromosome Analysis, Tissue

Institute for Genomic Medicine (IGM) Clinical Laboratory Nationwide Children's Hospital
United States
3231
  • K Karyotyping

5-Cell Confirmation Chromosome Analysis, Amniotic Fluid

Institute for Genomic Medicine (IGM) Clinical Laboratory Nationwide Children's Hospital
United States
3231
  • K Karyotyping

5-Cell Confirmation Chromosome Analysis, Peripheral Blood

Institute for Genomic Medicine (IGM) Clinical Laboratory Nationwide Children's Hospital
United States
3231
  • K Karyotyping

Chromosome Analysis (High Resolution), Cord Blood

Institute for Genomic Medicine (IGM) Clinical Laboratory Nationwide Children's Hospital
United States
3231
  • K Karyotyping

Results: 21 to 40 of 811

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.