Clinical and research tests for C0027708 - Genetic Testing Registry (GTR) - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

<< First < Prev

Page 3 of 3

Next >Last >>

Results: 41 to 57 of 57

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Invitae Renal/Urinary Tract Cancers Panel Invitae United States	37	24	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Multi-Cancer Panel Invitae United States	139	80	D Deletion/duplication analysis C Sequence analysis of the entire coding region
WT1 Sequencing Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States	2	1	C Sequence analysis of the entire coding region T Targeted variant analysis
Cancer Predisposition Asper Biogene Asper Biogene LLC Estonia	135	98	D Deletion/duplication analysis C Sequence analysis of the entire coding region
GPC3 Single Gene Fulgent Genetics United States	2	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
H19 Single Gene Fulgent Genetics United States	4	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
WT1 Single Gene Fulgent Genetics United States	8	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
BRCA2 Single Gene Fulgent Genetics United States	8	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Steroid-Resistant Nephrotic Syndrome NGS Panel Fulgent Genetics United States	24	14	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Clinical Exome Fulgent Genetics United States	5129	4672	D Deletion/duplication analysis C Sequence analysis of the entire coding region
XLID (X-Linked Intellectual Disability) NGS Panel Fulgent Genetics United States	162	117	D Deletion/duplication analysis C Sequence analysis of the entire coding region
BRCA1 and BRCA2 Focus Fulgent Genetics United States	10	2	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Intellectual Disability NGS Panel Fulgent Genetics United States	1058	554	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Lysosomal Disorders NGS Panel Fulgent Genetics United States	186	106	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Fanconi Anemia NGS Panel Fulgent Genetics United States	30	18	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Cardiovascular NGS Panel Fulgent Genetics United States	671	250	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Wilms' tumor Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders Germany	1	2	D Deletion/duplication analysis C Sequence analysis of the entire coding region

<< First < Prev

Page 3 of 3

Next >Last >>

Results: 41 to 57 of 57

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.