OSC5251 AND nstd224 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv6625935	copy number variation	60	nstd224	human	GRCh37 chr1: 189,350,700-189,542,729 , GRCh38.p12 chr1: 189,381,570-189,573,599	LOC105371657
nsv6622122	copy number variation	288	nstd224	human	GRCh37 chr13: 21,729,252-21,746,637 , GRCh38.p12 chr13: 21,155,113-21,172,498	SKA3
nsv6621849	copy number variation	162	nstd224	human	GRCh37 chr12: 8,003,758-8,123,306 , GRCh38.p12 chr12: 7,851,162-7,970,710	SLC2A14, RPS20P29, 3 more genes
nsv6633987	copy number variation	1	nstd224	human	GRCh37 chr9: 31,394,143-32,082,616 , GRCh38.p12 chr9: 31,394,145-32,082,618	HMGB3P23, LOC105376010, 4 more genes
nsv6626284	copy number variation	61	nstd224	human	GRCh37 chr1: 752,566-846,808 , GRCh38.p12 chr1: 817,186-911,428	LINC00115, FAM41C, 5 more genes
nsv6627488	copy number variation	1	nstd224	human	GRCh37 chr2: 10,637,325-10,661,047 , GRCh38.p12 chr2: 10,497,199-10,520,921	0