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Results: 1 to 20 of 17428

Tests names and labsConditionsGenes, analytes, and microbesMethods

CentoGenome (Whole Genome Sequencing)

Centogene AG - the Rare Disease Company
Germany
12
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CentoXome (Whole Exome Sequencing)

Centogene AG - the Rare Disease Company
Germany
12
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • U Uniparental disomy study (UPD)

Whole Exome Sequencing

DNA Labs India
India
11
  • C Sequence analysis of the entire coding region

Genomic Unity® Hearing Loss Disorders Analysis

Variantyx, Inc.
United States
1318
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Genomic Unity® Nuclear Encoded Mitochondrial Gene Analysis

Variantyx, Inc.
United States
1335
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Whole Genome Sequencing Reanalysis, WGSR

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

Whole Genome Sequencing for Hereditary Disorders, WGSDX

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

CentoXome MOx (Whole Exome Sequencing)

Centogene AG - the Rare Disease Company
Germany
1319
  • A Analyte
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • U Uniparental disomy study (UPD)

Carrier Screening Guidelines-Based Panel

Ambry Genetics
United States
199164
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Carrier Screening Comprehensive Panel

Ambry Genetics
United States
11
  • C Sequence analysis of the entire coding region

Carrier Screening CF+SMA

Ambry Genetics
United States
42
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

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

PGnome Rapid

PreventionGenetics, part of Exact Sciences
United States
11
  • C Sequence analysis of the entire coding region

PGnome Health Screen

PreventionGenetics, part of Exact Sciences
United States
11
  • C Sequence analysis of the entire coding region

PGxome Prenatal

PreventionGenetics, part of Exact Sciences
United States
11
  • C Sequence analysis of the entire coding region

PGxome Rapid

PreventionGenetics, part of Exact Sciences
United States
11
  • C Sequence analysis of the entire coding region

IriSightTM Prenatal Analysis - Proband

Variantyx, Inc.
United States
12
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Genomic Unity Exome Analysis - Proband (includes STR analysis of 36 loci)

Variantyx, Inc.
United States
11
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

NephrolithiasisNext™

Ambry Genetics
United States
131
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PGnome Diagnostic

PreventionGenetics, part of Exact Sciences
United States
11
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 17428

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.