dbVar for OMIM (Select 301500) - dbVar - NCBI

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Items: 5

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Number of Variants: 5

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4728362	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 101,397,821-101,402,341 , GRCh37 chrX: 100,652,809-100,657,329	GLA, RPL36A-HNRNPH2
nsv4728224	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 100,652,778-100,655,653 , GRCh38.p12 chrX: 101,397,790-101,400,665	GLA, RPL36A-HNRNPH2
nsv4683521	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrX: 100,656,225-100,658,983 , GRCh38.p12 chrX: 101,401,237-101,403,995	GLA, RPL36A-HNRNPH2
nsv4451469	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 100,658,779-100,658,993 , GRCh38 chrX: 101,403,791-101,404,005	GLA, RPL36A-HNRNPH2
nsv997088	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 100,652,779-100,663,001 , GRCh38.p12 chrX: 101,397,791-101,408,013	GLA, HNRNPH2, 1 more genes

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