Clinical and research tests for NF1 - Genetic Testing Registry (GTR)

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Results: 21 to 40 of 497

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Hereditary Common Cancer Panel Mayo Clinic Laboratories Mayo Clinic United States	1	36	C Sequence analysis of the entire coding region
Hereditary Expanded Cancer Panel Mayo Clinic Laboratories Mayo Clinic United States	1	86	C Sequence analysis of the entire coding region
Hereditary Breast/Gyn Cancer Panel Mayo Clinic Laboratories Mayo Clinic United States	1	20	C Sequence analysis of the entire coding region
qChip 1M Quantitative Genomic Medicine Laboratories, SL Spain	184	162	D Deletion/duplication analysis
qChip 60k post-natal Quantitative Genomic Medicine Laboratories, SL Spain	184	162	D Deletion/duplication analysis
qChip 400 Quantitative Genomic Medicine Laboratories, SL Spain	184	162	D Deletion/duplication analysis
Microdeletion / Microduplication Syndromes Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS Chile	28	39	D Deletion/duplication analysis
High-Resolution Rapid Microarray (CGH and SNP) Allele Diagnostics United States	247	231	D Deletion/duplication analysis H Detection of homozygosity
Tempus xT Tempus AI - CHI United States	2	647	I Microsatellite instability testing (MSI) C Sequence analysis of the entire coding region
Otogenetics Hereditary Cancers Otogenetics United States	36	39	E Sequence analysis of select exons
RASopathy NGS Panel UAB Medical Genomics Laboratory UAB Medicine United States	8	18	D Deletion/duplication analysis 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
Onco microarray for MDS/AML Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center United States	2	69	D Deletion/duplication analysis H Detection of homozygosity
Rapid microarray (CGH and SNP) Allele Diagnostics United States	247	231	D Deletion/duplication analysis H Detection of homozygosity
NOONAN SYNDROME Clinical Genomics Unit Hospital Universitari Germans Trias i Pujol Spain	5	16	D Deletion/duplication analysis E Sequence analysis of select exons C Sequence analysis of the entire coding region
RASOPATHY-RELATED SYNDROME Clinical Genomics Unit Hospital Universitari Germans Trias i Pujol Spain	9	19	D Deletion/duplication analysis E Sequence analysis of select exons C Sequence analysis of the entire coding region
qChip 60k prenatal Quantitative Genomic Medicine Laboratories, SL Spain	184	162	D Deletion/duplication analysis
NEUROFIBROMATOSIS TYPE 1 - NF1 gene Clinical Genomics Unit Hospital Universitari Germans Trias i Pujol Spain	2	2	D Deletion/duplication analysis L Linkage analysis E Sequence analysis of select exons C Sequence analysis of the entire coding region
LEGIUS SYNDROME - SPRED1 gene Clinical Genomics Unit Hospital Universitari Germans Trias i Pujol Spain	2	2	D Deletion/duplication analysis L Linkage analysis X Mutation scanning of select exons C Sequence analysis of the entire coding region
Tempus xF Tempus AI - RTP United States	1	105	I Microsatellite instability testing (MSI) C Sequence analysis of the entire coding region

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Results: 21 to 40 of 497

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: 21 to 40 of 497

Results: 21 to 40 of 497