OSC2463 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
nsv6632638	copy number variation	1	nstd224	human		GRCh37 chr8: 4,566,521-4,627,197 , GRCh38.p12 chr8: 4,708,999-4,769,675	CSMD1
nsv6625733	copy number variation	79	nstd224	human		GRCh37 chr1: 213,005,012-213,020,221 , GRCh38.p12 chr1: 212,831,670-212,846,879	SPATA45
nsv6626813	copy number variation	12	nstd224	human		GRCh37 chr21: 10,906,922-10,942,992 , GRCh38.p12 chr21: 10,569,465-10,605,535	TPTE, CYCSP41
nsv6621730	copy number variation	83	nstd224	human		GRCh37 chr12: 63,946,056-64,116,159 , GRCh38.p12 chr12: 63,552,276-63,722,379	LOC100418730, S100A11P4, 1 more genes
nsv6625550	copy number variation	22	nstd224	human		GRCh37 chr1: 121,171,208-121,289,118 , GRCh38.p12 chr1: 121,429,348-121,547,320	LINC02798, MTIF2P1, 1 more genes
nsv6633831	copy number variation	3	nstd224	human		GRCh37 chrX: 134,947,910-135,004,640 , GRCh38.p12 chrX: 135,779,396-135,922,481	SAGE1, CT45A5, 6 more genes
nsv6630942	copy number variation	2	nstd224	human		GRCh37 chr6: 168,348,583-168,592,134 , GRCh38.p12 chr6: 167,947,903-168,191,454	KIF25, AFDN, 5 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
nsv6621016	copy number variation	8	nstd224	human		GRCh37 chr11: 67,501,626-67,748,817 , GRCh38.p12 chr11: 67,734,155-67,981,346	EVA1CP4, LOC105369358, 11 more genes
nsv6622369	copy number variation	248	nstd224	human		GRCh37 chr14: 20,213,937-20,420,151 , GRCh38.p12 chr14: 19,745,778-19,951,992	OR4N1P, OR4K1, 10 more genes

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