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Results: 1 to 9 of 9

Tests names and labsConditionsGenes, analytes, and microbesMethods

PGmax™ - Neonatal Crisis Panel

PreventionGenetics, part of Exact Sciences
United States
211
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Constitutional Chromosomal Microarray Analysis

Clinical Genomics Laboratory Laboratory for Precision Diagnostics, University of Washington
United States
261
  • D Deletion/duplication analysis

Chromosomal Microarray Analysis

CIBIC S.A.
Argentina
51
  • D Deletion/duplication analysis

Chromosome Analysis, Blood w/ reflex to Postnatal ClariSure Oligo/SNP array

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
51
  • K Karyotyping
  • D Deletion/duplication analysis

Chromosomal Microarray, Postnatal, ClariSure, Oligo/SNP

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
51
  • D Deletion/duplication analysis

Chromosome Analysis, Blood w/ reflex to Postnatal ClariSure Oligo/SNP array

Quest Diagnostics Nichols Institute Chantilly
United States
51
  • K Karyotyping
  • D Deletion/duplication analysis

Chromosomal Microarray, Postnatal, ClariSure, Oligo/SNP

Quest Diagnostics Nichols Institute Chantilly
United States
51
  • D Deletion/duplication analysis

ArrayCGH, Postnatal

MGZ Medical Genetics Center
Germany
61
  • D Deletion/duplication analysis

Array SNP-Based Analysis

Cytogenomics Laboratory Johns Hopkins Hospital
United States
51
  • D Deletion/duplication analysis

Results: 1 to 9 of 9

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.