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Results: 61 to 77 of 77

Tests names and labsConditionsGenes, analytes, and microbesMethods

Microphthalmia, Anophthalmia, and Coloboma Panel NGS Panel

Fulgent Genetics
United States
24478
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Manitoba Oculotrichoanal Syndrome: gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • C Sequence analysis of the entire coding region

Manitoba Oculotrichoanal Syndrome: gene deletion/duplication

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • D Deletion/duplication analysis

Anophthalmia/microphthalmia

Department of Clinical Genetics Copenhagen University Hospital, Rigshospitalet
Denmark
1129
  • C Sequence analysis of the entire coding region

Craniosynostosis Panel

Blueprint Genetics
Finland
137
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Microphthalmia, Anophthalmia and Anterior Segment Dysgenesis Panel

Blueprint Genetics
Finland
354
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Renal Malformation Panel

Blueprint Genetics
Finland
122
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Single gene testing FREM1

CeGaT GmbH
Germany
31
  • C Sequence analysis of the entire coding region

Nephrology Endocrinology and Electrolytes - panels

MGZ Medical Genetics Center
Germany
5117
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Craniosynostosis syndromes Panel

CeGaT GmbH
Germany
2020
  • C Sequence analysis of the entire coding region

CAKUT

Hildebrandt Laboratory Boston Children's Hospital
United States
2204
  • C Sequence analysis of the entire coding region

Microphthalmy Panel

CeGaT GmbH
Germany
1326
  • C Sequence analysis of the entire coding region

Renal Dysplasia, Renal Agenesia, CAKUT Panel

CeGaT GmbH
Germany
132
  • C Sequence analysis of the entire coding region

FREM1 Single Gene

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Fraser syndrome panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
44
  • C Sequence analysis of the entire coding region

Comprehensive Eye Disorders NGS Panel

Fulgent Genetics
United States
1018459
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 61 to 77 of 77

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.