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Results: 1 to 20 of 43

Tests names and labsConditionsGenes, analytes, and microbesMethods

qChip 1M

Quantitative Genomic Medicine Laboratories, SL
Spain
184162
  • D Deletion/duplication analysis

qChip 60k post-natal

Quantitative Genomic Medicine Laboratories, SL
Spain
184162
  • D Deletion/duplication analysis

qChip 400

Quantitative Genomic Medicine Laboratories, SL
Spain
184162
  • D Deletion/duplication analysis

Microdeletion / Microduplication Syndromes

Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS
Chile
2839
  • D Deletion/duplication analysis

High-Resolution Rapid Microarray (CGH and SNP)

Allele Diagnostics
United States
247231
  • D Deletion/duplication analysis
  • H Detection of homozygosity

1p36 deletion syndrome FISH

Cytogenetics Laboratory University of Washington
United States
11
  • M FISH-metaphase

Rapid microarray (CGH and SNP)

Allele Diagnostics
United States
247231
  • D Deletion/duplication analysis
  • H Detection of homozygosity

qChip 60k prenatal

Quantitative Genomic Medicine Laboratories, SL
Spain
184162
  • D Deletion/duplication analysis

Chromosomal microarray

Michigan Medical Genetics Laboratories University of Michigan
United States
181
  • D Deletion/duplication analysis

Panorama Non-invasive Prenatal Test

Natera, Inc.
United States
1210
  • T Targeted variant analysis

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

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

Chromosome Analysis, Amniotic Fluid

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

STAT Chromosome Analysis, Peripheral Blood

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

Chromosome Analysis, Tissue (Postnatal, POC, or Autopsy)

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

Chromosome Analysis (High Resolution), Peripheral Blood

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

Chromosome 1p36 deletion syndrome, 607872, Isolated cases (1p36 deletion syndrome) (Prenatal) (440)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Results: 1 to 20 of 43

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.