Clinical and research tests for C0017668 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
FSGS/Nephrotic Syndrome Gene Panel Mayo Clinic Laboratories Mayo Clinic United States	25	56	D Deletion/duplication analysis C Sequence analysis of the entire coding region
APOL1 Testing: G1 and G2 alleles Iowa Institute of Human Genetics University of Iowa United States	1	1	T Targeted variant analysis
PGmax™ - Comprehensive Inherited Kidney Disease Panel PreventionGenetics, part of Exact Sciences United States	10	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
RenalZoom Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins Hospital United States	527	338	C Sequence analysis of the entire coding region
Nephrotic syndrome and related disorders Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States	39	42	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Nephrotic syndrome and related disorders NGS panel HNL Genomics Connective Tissue Gene Tests United States	39	42	C Sequence analysis of the entire coding region T Targeted variant analysis
Nephrotic syndrome and related disorders Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States	39	42	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Hereditary Cystic and Glomerular Disorders Panel Genetic Services Laboratory University of Chicago United States	17	64	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Inherited Renal Disorders Panel Dhiti Omics Technologies Private Ltd India	72	57	C Sequence analysis of the entire coding region
Nephrotic Syndrome/Focal Segmental Glomerulosclerosis GeneDx United States	3	55	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Kidney Genetics Mutation Panel Molecular Genetics University of North Carolina Hospitals United States	3	16	C Sequence analysis of the entire coding region
Comprehensive Glomerular Proteinuria NGS Panel Fulgent Genetics United States	182	76	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Early-Onset Ataxia NGS Panel Fulgent Genetics United States	505	132	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Ataxia NGS Panel Fulgent Genetics United States	533	149	D Deletion/duplication analysis C Sequence analysis of the entire coding region
STEROID-RESISTANT NEPHROTIC SYNDROME WITH FOCAL SEGMENTAL GLOMERULOSCLEROSIS. Laboratorio de Genetica Clinica SL Spain	6	9	C Sequence analysis of the entire coding region
Focal segmental glomerulosclerosis Institute of Human Genetics Cologne University Germany	2	2	C Sequence analysis of the entire coding region
Cystic Disease and Nephronopthisis panel Clinical Genomics Laboratory Washington University in St. Louis United States	16	33	C Sequence analysis of the entire coding region
WDR73 Single Gene Fulgent Genetics United States	66	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
ANLN Single Gene Fulgent Genetics United States	4	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
NXF5 Single Gene Fulgent Genetics United States	1	1	D Deletion/duplication analysis 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.