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Results: 1 to 20 of 83

Tests names and labsConditionsGenes, analytes, and microbesMethods

Chromosomal Microarray

Genetics Laboratory Shodair Children's Hospital
United States
71
  • D Deletion/duplication analysis
  • H Detection of homozygosity

SNP based chromosomal microarray

Al Jalila Children's Genomics Center Al Jalila Childrens Speciality Hospital
United Arab Emirates
51
  • D Deletion/duplication analysis
  • H Detection of homozygosity
  • U Uniparental disomy study (UPD)

Familial Targeted Microarray

Ambry Genetics
United States
31
  • D Deletion/duplication analysis

Droplet digital PCR

Clinical Genomics Laboratory Laboratory for Precision Diagnostics, University of Washington
United States
11
  • D Deletion/duplication analysis

SNP Array

Ambry Genetics
United States
31
  • D Deletion/duplication analysis

Anora Products of Conception Testing

Natera, Inc.
United States
41
  • K Karyotyping
  • D Deletion/duplication analysis
  • H Detection of homozygosity
  • U Uniparental disomy study (UPD)

Constitutional Chromosomal Microarray Analysis

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

SNP microarray (Reveal)

Clinical Cytogenetics Laboratory LabCorp
United States
31
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Chromosomal Microarray Analysis

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

SNP Microarray

Genetics Laboratory Dayton Children's Hospital
United States
21
  • D Deletion/duplication analysis

Chromosome FISH with Reflex to Chromosome Analysis or Genomic Microarray

ARUP Laboratories, Cytogenetics and Genomic Microarray ARUP Laboratories
United States
121
  • I FISH-interphase
  • K Karyotyping
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Chromosome Analysis with Reflex to Genomic Microarray

ARUP Laboratories, Cytogenetics and Genomic Microarray ARUP Laboratories
United States
161
  • K Karyotyping
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Chromosome Microarray

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
61
  • D Deletion/duplication analysis

Spinal Muscular Atrophy NGS Panel

Fulgent Genetics
United States
9329
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Metabolism NGS Panel

Fulgent Genetics
United States
602355
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Childhood Epilepsy NGS Panel

Fulgent Genetics
United States
354209
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Hearing Loss NGS Panel

Fulgent Genetics
United States
332167
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neonatal Epilepsy NGS Panel

Fulgent Genetics
United States
509275
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Retinopathy and Optic Atrophy NGS Panel

Fulgent Genetics
United States
563241
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Early-Onset Ataxia NGS Panel

Fulgent Genetics
United States
505132
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 83

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.