Clinical and research tests for 613236 - Genetic Testing Registry (GTR)

Results: 1 to 16 of 16

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Osteogenesis Imperfecta Genetic Panel MNG Laboratories (Medical Neurogenetics, LLC.) United States	28	19	C Sequence analysis of the entire coding region
KCNJ18 Gene Thyrotoxic periodic paralysis type 2 NGS Genetic DNA Test DNA Labs India India	1	1	S Mutation scanning of the entire coding region
UCHL1 Gene PARK5 Parkinson NGS Genetic DNA Test DNA Labs India India	1	1	S Mutation scanning of the entire coding region
Thyrotoxic periodic paralysis, susceptibility to, 2, 613239, Isolated cases; TTPP2 (Thyrotoxic periodic paralysis) (KCNJ18 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
GeneSeq® Neuro: Hypokalemic and Hyperkalemic Periodic Paralysis Panel MNG Laboratories (Medical Neurogenetics, LLC.) United States	6	5	C Sequence analysis of the entire coding region
Non-dystrophic myotonias and periodic paralysis (WES based NGS panel of 13 genes, including CNV analysis) CGC Genetics Unilabs Portugal	1	13	C Sequence analysis of the entire coding region
Thyrotoxic periodic paralysis type 2 (sequence analysis of KCNJ18 gene) CGC Genetics Unilabs Portugal	1	1	C Sequence analysis of the entire coding region
Genomic Unity® Custom Analysis Variantyx, Inc. United States	1	4054	D Deletion/duplication analysis X Mutation scanning of select exons C Sequence analysis of the entire coding region
Thyrotoxic periodic paralysis: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	2	2	C Sequence analysis of the entire coding region
KCNJ18 Single Gene Fulgent Genetics United States	1	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hypokalemic Periodic Paralysis: gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	1	3	C Sequence analysis of the entire coding region
PERIODIC PARALYSIS, HYPOKALEMIC Laboratorio de Genetica Clinica SL Spain	4	4	E Sequence analysis of select exons C Sequence analysis of the entire coding region
PERIODIC PARALYSIS, THYROTOXIC Laboratorio de Genetica Clinica SL Spain	2	2	C Sequence analysis of the entire coding region
KCNJ18 Sequencing Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States	1	1	C Sequence analysis of the entire coding region T Targeted variant analysis
Bartter Syndrome incl. differential diagnosis Panel CeGaT GmbH Germany	10	6	C Sequence analysis of the entire coding region
Clinical Exome Fulgent Genetics United States	5128	4672	D Deletion/duplication analysis C Sequence analysis of the entire coding region

Results: 1 to 16 of 16

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Results: 1 to 16 of 16

Results: 1 to 16 of 16