Clinical and research tests for C1865872 - Genetic Testing Registry (GTR)

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Results: 41 to 60 of 80

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Cholestasis NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	104	73	C Sequence analysis of the entire coding region
INVS Gene Sequencing by Massively Parallel Sequencing (BCM-NGSSM) Baylor Genetics United States	1	1	E Sequence analysis of select exons
INVS Sequence Analysis (Familial Mutation/Variant Analysis) Baylor Genetics United States	1	1	T Targeted variant analysis
INVS Sequence Analysis (Prenatal Sequence Analysis) Baylor Genetics United States	1	1	E Sequence analysis of select exons
Nephronophthisis Asper Biogene Asper Biogene LLC Estonia	44	20	C Sequence analysis of the entire coding region
Ciliopathies Asper Biogene Asper Biogene LLC Estonia	166	120	C Sequence analysis of the entire coding region
Comprehensive lung panel Al Jalila Children's Genomics Center Al Jalila Childrens Speciality Hospital United Arab Emirates	64	66	C Sequence analysis of the entire coding region
Primary Ciliary Dyskinesia panel Al Jalila Children's Genomics Center Al Jalila Childrens Speciality Hospital United Arab Emirates	36	38	C Sequence analysis of the entire coding region
Nephronophthisis: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	14	13	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
Comprehensive Primary Immunodeficiency NGS Panel Fulgent Genetics United States	1048	472	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Primary Ciliary Dyskinesia NGS Panel Fulgent Genetics United States	55	38	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Congenital Heart Defect NGS Panel Fulgent Genetics United States	377	114	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Nephronophthisis Institute of Human Genetics Cologne University Germany	5	4	D Deletion/duplication analysis S Mutation scanning of the entire coding region C Sequence analysis of the entire coding region
Senior-Loken Syndrome Asper Biogene Asper Biogene LLC Estonia	19	9	C Sequence analysis of the entire coding region
Nephronophthisis , Panel Massive Sequencing (NGS) 11 Genes Reference Laboratory Genetics Spain	11	11	C Sequence analysis of the entire coding region
NEPHRONOPHTHISIS TYPE 2 (INFANTILE) Laboratorio de Genetica Clinica SL Spain	1	1	C Sequence analysis of the entire coding region
Primary Ciliary Dyskinesia & Cystic Fibrosis NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	45	42	C Sequence analysis of the entire coding region
Comprehensive Pulmonary NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	123	124	C Sequence analysis of the entire coding region
Infantile Nephronophthisis Type 2, Sequencing INVS Gene Reference Laboratory Genetics Spain	1	1	C Sequence analysis of the entire coding region

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Results: 41 to 60 of 80

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: 41 to 60 of 80

Results: 41 to 60 of 80