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Results: 21 to 40 of 119

Tests names and labsConditionsGenes, analytes, and microbesMethods

Chromosomal microarray analysis (aCGH, Cytoscan 750K), prenatal test

CGC Genetics Unilabs
Portugal
51
  • K Karyotyping

Reanalysis and interpretation microarray analysis (aCGH, Cytoscan 750K)

CGC Genetics Unilabs
Portugal
51
  • K Karyotyping

Reanalysis and interpretation microarray analysis (aCGH, Cytoscan HD)

CGC Genetics Unilabs
Portugal
51
  • K Karyotyping

Chromosomal Microarray Analysis

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

Whole Exome Sequencing (WES)

Duzen Laboratories Duzen BBAGUAS
Turkey
51
  • C Sequence analysis of the entire coding region

Clinical Exome Sequencing (CES)

Duzen Laboratories Duzen BBAGUAS
Turkey
51
  • C Sequence analysis of the entire coding region

InSight (FISH for 13, 18, 21, X & Y)

Integrated Genetics Cytogenetics and Biochemistry Laboratory
United States
41
  • I FISH-interphase

Chromosome Analysis

Integrated Genetics Cytogenetics and Biochemistry Laboratory
United States
41
  • K Karyotyping

SNP Microarray

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

Cytogenomic Molecular Inversion Probe Array FFPE Tissue - Products of Conception

ARUP Laboratories, Cytogenetics and Genomic Microarray ARUP Laboratories
United States
151
  • K Karyotyping

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: 21 to 40 of 119

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.