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Results: 1 to 13 of 13

Tests names and labsConditionsGenes, analytes, and microbesMethods

Achondroplasia

Center for Genetics at Saint Francis Saint Francis Hospital
United States
21
  • E Sequence analysis of select exons

OmniSeek Whole Exome Sequencing

Juno Genomics Hangzhou Juno Genomics, Inc
China
1041
  • T Targeted variant analysis

Short Stature

Genetics Laboratory University of Oklahoma Health Sciences Center
United States
186
  • C Sequence analysis of the entire coding region

Hypomagnesemia NGS Panel

Fulgent Genetics
United States
12123
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Short Stature Syndrome Panel

Blueprint Genetics
Finland
475
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

TBX6 Single Gene

Fulgent Genetics
United States
271
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

LARP7 Single Gene

Fulgent Genetics
United States
101
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CRIPT Single Gene

Fulgent Genetics
United States
221
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FAM111A Single Gene

Fulgent Genetics
United States
901
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NIN Single Gene

Fulgent Genetics
United States
171
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Skeletal Dysplasias NGS Panel

Fulgent Genetics
United States
543178
  • 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

Microcephaly NGS Panel

Fulgent Genetics
United States
32275
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 13 of 13

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.