Clinical and research tests for C1846343 - Genetic Testing Registry (GTR) - NCBI

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Results: 21 to 40 of 45

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Bartter/Gitelman Syndromes (NGS Panel and Copy Number Analysis) MNG Laboratories (Medical Neurogenetics, LLC.) United States	6	8	C Sequence analysis of the entire coding region
Hypomagnesemia Asper Biogene Asper Biogene LLC Estonia	27	18	C Sequence analysis of the entire coding region
Bartter Syndrome Asper Biogene Asper Biogene LLC Estonia	36	24	C Sequence analysis of the entire coding region
Bartter syndrome: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	7	6	C Sequence analysis of the entire coding region
Hypomagnesemia NGS Panel Fulgent Genetics United States	121	23	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Bartter Syndrome NGS Panel Fulgent Genetics United States	39	27	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Familial Hypomagnesemia , Panel Massive Sequencing (NGS) 14 Genes Reference Laboratory Genetics Spain	16	14	C Sequence analysis of the entire coding region
Bartter Syndrome and related disorders , Panel Massive Sequencing (NGS) 22 Genes Reference Laboratory Genetics Spain	21	22	C Sequence analysis of the entire coding region
BARTTER SYNDROME, CLASSIC ,TYPE 3 Laboratorio de Genetica Clinica SL Spain	1	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Bartter Syndrome Type 3, Deletions-Duplications (MLPA) CLCNKB Gene Reference Laboratory Genetics Spain	1	1	D Deletion/duplication analysis
Bartter Syndrome Type 3, Sequencing CLCNKB Gene Reference Laboratory Genetics Spain	1	1	C Sequence analysis of the entire coding region
Bartter syndrome Institute of Human Genetics Cologne University Germany	10	6	C Sequence analysis of the entire coding region
CLCNKB Gene Sequencing and Deletion/Duplication Analysis DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children United States	2	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Bartter syndrome type 3 Bioarray Spain	1	1	C Sequence analysis of the entire coding region
Non-Immune Hydrops NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	86	87	C Sequence analysis of the entire coding region
Bartter Syndrome Panel CeGaT GmbH Germany	3	8	C Sequence analysis of the entire coding region
CLCNKB 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
CLCNKB Single Gene Fulgent Genetics United States	2	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hereditary Renal Tubular Disorders Evaluation Athena Diagnostics United States	6	5	C Sequence analysis of the entire coding region
CLCNKB DNA Sequencing Test Athena Diagnostics United States	2	1	C Sequence analysis of the entire coding region

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Results: 21 to 40 of 45

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.