Clinical and research tests for FGFR3 - Genetic Testing Registry (GTR)

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Guardant360 TissueNext Guardant Health United States	1	85	M Methylation analysis I Microsatellite instability testing (MSI) E Sequence analysis of select exons T Targeted variant analysis
Guardant360 Response Guardant Health United States	1	74	E Sequence analysis of select exons T Targeted variant analysis
NeXT Dx Personalis, Inc. United States	1	413	I Microsatellite instability testing (MSI) R RNA analysis C Sequence analysis of the entire coding region
Guardant360 Guardant Health United States	1	84	I Microsatellite instability testing (MSI) E Sequence analysis of select exons T Targeted variant analysis
Craniodysmorphology Panel (FGFR1,2,3,TWIST) Center for Genetics at Saint Francis Saint Francis Hospital United States	8	4	E Sequence analysis of select exons T Targeted variant analysis
Muenke Syndrome - FGFR3 Gene (PRO250ARG) Center for Genetics at Saint Francis Saint Francis Hospital United States	1	1	T Targeted variant analysis
Hypochondroplasia Center for Genetics at Saint Francis Saint Francis Hospital United States	1	1	T Targeted variant analysis
Crouzon Syndrome with Acanthosis Nigricans Center for Genetics at Saint Francis Saint Francis Hospital United States	1	1	E Sequence analysis of select exons
Achondroplasia Center for Genetics at Saint Francis Saint Francis Hospital United States	2	1	E Sequence analysis of select exons
Tempus xT Tempus AI - RTP United States	2	647	I Microsatellite instability testing (MSI) C Sequence analysis of the entire coding region
FGFR3 Gene Achondroplasia NGS Genetic DNA Test DNA Labs India India	1	1	S Mutation scanning of the entire coding region
FGFR3 Gene Crouzon syndrome with acanthosis nigricans NGS Genetic DNA Test DNA Labs India India	1	1	S Mutation scanning of the entire coding region
FGFR3 Gene Hypochondroplasia NGS Genetic DNA Test DNA Labs India India	1	1	S Mutation scanning of the entire coding region
OtoSCOPE v9 Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics United States	287	218	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Muenke syndrome (FGFR3 gene) Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS Chile	1	1	T Targeted variant analysis
Thanatophoric Dysplasia (FGFR3 gene) Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS Chile	2	1	T Targeted variant analysis
Tempus xT Tempus AI - CHI United States	2	647	I Microsatellite instability testing (MSI) C Sequence analysis of the entire coding region
Achondroplasia Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India	1	1	T Targeted variant analysis
Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel Otogenetics United States	122	128	E Sequence analysis of select exons
FoundationOne® Heme Foundation Medicine, Inc. United States	2	405	D Deletion/duplication analysis R RNA analysis E Sequence analysis of select exons C Sequence analysis of the entire coding region

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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.

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Results: 1 to 20 of 398

Results: 1 to 20 of 398