OSC2602 AND nstd224 - dbVar - NCBI

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Items: 9

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Number of Variants: 9

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6628914	copy number variation	179	nstd224	human		GRCh37 chr3: 173,259,356-173,289,281 , GRCh38.p12 chr3: 173,541,566-173,571,491	NLGN1
nsv6621689	copy number variation	1	nstd224	human		GRCh37 chr13: 42,293,761-42,314,903 , GRCh38.p12 chr13: 41,719,625-41,740,767	VWA8
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
nsv6621588	copy number variation	15	nstd224	human		GRCh37 chr12: 21,024,839-21,036,533 , GRCh38.p12 chr12: 20,871,905-20,883,599	SLCO1B3, SLCO1B3-SLCO1B7
nsv6623104	copy number variation	20	nstd224	human		GRCh37 chr15: 32,049,125-32,514,341 , GRCh38.p12 chr15: 31,756,922-32,222,140 , GRCh38.p12 chr15\|NT_187660.1: 4,042,024-4,507,812 , GRCh38.p12 chr15\|NW_011332701.1: 3,929,572-4,395,360	OTUD7A, LOC102724078, 2 more genes
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
nsv6625794	copy number variation	1	nstd224	human		GRCh37 chr1: 1,635,272-1,684,472 , GRCh38.p12 chr1: 1,703,833-1,753,033	SLC35E2A, NADK, 3 more genes
nsv6631445	copy number variation	586	nstd224	human		GRCh37 chr6: 67,017,543-67,044,431 , GRCh38.p12 chr6: 66,307,650-66,334,538	0
nsv6623576	copy number variation	1	nstd224	human		GRCh37 chr16: 21,624,036-21,966,869 , GRCh38.p12 chr16: 21,612,715-21,955,548 , GRCh38.p12 chr16\|NW_017852933.1: 1,149,490-1,492,127	IGSF6, METTL9, 12 more genes

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