OSC3426 AND nstd224 - dbVar - NCBI

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Items: 10

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Number of Variants: 10

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6622928	copy number variation	62	nstd224	human		GRCh37 chr15: 87,837,388-87,861,276 , GRCh38.p12 chr15: 87,294,157-87,318,045	LOC107984735
nsv6630360	copy number variation	23	nstd224	human		GRCh37 chr5: 61,772,530-61,800,698 , GRCh38.p12 chr5: 62,476,703-62,504,871	IPO11
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
nsv6628062	copy number variation	29	nstd224	human		GRCh37 chr2: 228,243,816-228,254,272 , GRCh38.p12 chr2: 227,379,100-227,389,556	TM4SF20
nsv6622312	copy number variation	21	nstd224	human		GRCh37 chr14: 45,618,040-45,628,478 , GRCh38.p12 chr14: 45,148,837-45,159,275	FANCM
nsv6625409	copy number variation	10	nstd224	human		GRCh37 chr1: 1,597,351-1,611,995 , GRCh38.p12 chr1: 1,665,912-1,680,556	LOC100288379, SLC35E2B
nsv6631923	copy number variation	1	nstd224	human		GRCh37 chr7: 66,726,274-66,962,579 , GRCh38.p12 chr7: 67,261,287-67,497,592	STAG3L4, SPDYE21, 3 more genes
nsv6627055	copy number variation	71	nstd224	human		GRCh37 chr22: 18,892,575-19,008,108 , GRCh38.p12 chr22: 18,905,062-19,020,595	DGCR6, PRODH, 1 more genes
nsv6621457	copy number variation	226	nstd224	human		GRCh37 chr12: 31,266,287-31,406,907 , GRCh38.p12 chr12: 31,113,353-31,253,973 , GRCh38.p12 chr12\|NT_187587.1: 1,874-144,767	OVOS2, RPL13AP22, 6 more genes
nsv6632147	copy number variation	132	nstd224	human		GRCh37 chr7: 44,935-67,365 , GRCh38.p12 chr7: 44,935-67,365 , GRCh38.p12 chr7\|NT_187558.1: 1,034-23,464 , GRCh38.p12 chr7\|NT_187653.1: 37,256-59,686	0

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