Clinical and research tests for 162000 - Genetic Testing Registry (GTR) - NCBI

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Results: 21 to 40 of 55

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Polycystic kidney disease and related disorders Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States	29	22	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Polycystic kidney disease and related disorders NGS panel HNL Genomics Connective Tissue Gene Tests United States	28	21	C Sequence analysis of the entire coding region T Targeted variant analysis
Invitae Purine Metabolism Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States	26	18	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Congenital Abnormalities of the Kidney and Urinary Tract (CAKUT) Panel PreventionGenetics, part of Exact Sciences United States	82	78	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Medullary Cystic Kidney Disease type 2 and Familial Juvenile Hyperuricemic Nephropathy type 1 via the UMOD Gene PreventionGenetics, part of Exact Sciences United States	1	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
UMOD Institute for Human Genetics University Medical Center Freiburg Germany	1	1	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
Polycystic Kidney Disease Asper Biogene Asper Biogene LLC Estonia	38	23	C Sequence analysis of the entire coding region
Hyperuricemic nephropathy, familial juvenile: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	3	3	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
Expanded Polycystic Kidney Disease NGS Panel Fulgent Genetics United States	61	34	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Uromodulin-Associated Kidney Disease (UMOD Single Gene Test) Fulgent Genetics United States	1	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Kidney Dysplasia NGS Panel Fulgent Genetics United States	68	41	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Medullary Cystic Kidney Disease 2: UMOD Gene Sequencing CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	1	1	C Sequence analysis of the entire coding region
Medullary Cystic Kidney Disease 2: UMOD Gene Deletion/Duplication CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	1	1	D Deletion/duplication analysis
MEDULLARY CYSTIC KIDNEY DISEASE TYPE 2 (MCKD2) Laboratorio de Genetica Clinica SL Spain	1	1	C Sequence analysis of the entire coding region
HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE TYPE1 Laboratorio de Genetica Clinica SL Spain	1	1	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
Hereditary Tubulopathy and Nephrolithiasis Panel Genetic Services Laboratory University of Chicago United States	12	75	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Familial juvenile hyperuricemic nephropathy type 1 Bioarray Spain	1	1	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.