OSC5600 AND nstd224 - dbVar - NCBI

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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
nsv6632053	copy number variation	15	nstd224	human		GRCh37 chr7: 16,358,315-16,389,412 , GRCh38.p12 chr7: 16,318,690-16,349,787	CRPPA
nsv6627728	copy number variation	2	nstd224	human		GRCh37 chr2: 182,030,229-182,399,628 , GRCh38.p12 chr2: 181,165,502-181,534,901	MIR4437, ITGA4, 2 more genes
nsv6630572	copy number variation	14	nstd224	human		GRCh37 chr5: 178,754,468-178,931,310 , GRCh38.p12 chr5: 179,327,467-179,504,309 , GRCh38.p12 chr5\|NW_016107298.1: 92,174-268,949	ADAMTS2, LOC107986494, 1 more genes
nsv6634078	copy number variation	1	nstd224	human		GRCh37 chrX: 77,181,004-77,312,616 , GRCh38.p12 chrX: 77,925,507-78,057,119	ATP7A, C4orf46P2, 1 more genes
nsv6625644	copy number variation	1	nstd224	human		GRCh37 chr1: 151,341,499-151,407,693 , GRCh38.p12 chr1: 151,369,023-151,435,217	SELENBP1, POGZ, 1 more genes
nsv6623511	copy number variation	61	nstd224	human		GRCh37 chr16: 75,539,436-75,577,559 , GRCh38.p12 chr16: 75,505,538-75,543,661	CHST5, TMEM231, 1 more genes
nsv6631041	copy number variation	21	nstd224	human		GRCh37 chr6: 31,360,255-31,453,618 , GRCh38.p12 chr6: 31,392,478-31,485,841	HCP5, HLA-X, 5 more genes
nsv6621198	copy number variation	43	nstd224	human		GRCh37 chr11: 67,501,626-67,731,956 , GRCh38.p12 chr11: 67,734,155-67,964,485	RPS3AP40, EVA1CP4, 10 more genes
nsv6620265	copy number variation	201	nstd224	human		GRCh37 chr10: 135,256,762-135,379,710 , GRCh38.p12 chr10: 133,443,258-133,566,206	CYP2E1, OR7M1P, 4 more genes
nsv6630369	copy number variation	1	nstd224	human		GRCh37 chr5: 6,804,983-7,418,630 , GRCh38.p12 chr5: 6,804,870-7,418,517	LOC100130063, RNA5SP176, 15 more genes

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