OSC6802 AND nstd224 - dbVar - NCBI

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6630814	copy number variation	62	nstd224	human		GRCh37 chr5: 97,051,856-97,096,042 , GRCh38.p12 chr5: 97,716,152-97,760,338	LOC391813
nsv6628670	copy number variation	44	nstd224	human		GRCh37 chr3: 165,041,791-165,079,776 , GRCh38.p12 chr3: 165,324,003-165,361,988	LINC01322
nsv6625538	copy number variation	421	nstd224	human		GRCh37 chr1: 110,228,436-110,241,385 , GRCh38.p12 chr1: 109,685,814-109,698,763	GSTM1
nsv6628003	copy number variation	118	nstd224	human		GRCh37 chr2: 228,241,621-228,258,199 , GRCh38.p12 chr2: 227,376,905-227,393,483	TM4SF20
nsv6626075	copy number variation	20	nstd224	human		GRCh37 chr1: 196,821,486-196,876,278 , GRCh38.p12 chr1: 196,852,356-196,907,148	CFHR4, LOC100996886
nsv6626369	copy number variation	153	nstd224	human		GRCh37 chr1: 25,604,951-25,655,563 , GRCh38.p12 chr1: 25,278,460-25,329,072	RSRP1, RHD, 1 more genes
nsv6625753	copy number variation	40	nstd224	human		GRCh37 chr1: 12,901,323-12,921,386 , GRCh38.p12 chr1: 12,841,470-12,861,531 , GRCh38.p12 chr1\|NW_012132914.1: 22,983-43,044	PRAMEF30P, HNRNPCL1, 1 more genes
nsv6633008	copy number variation	1	nstd224	human		GRCh37 chr8: 56,711,713-56,869,323 , GRCh38.p12 chr8: 55,799,154-55,956,764	TGS1, LYN, 1 more genes
nsv6630383	copy number variation	69	nstd224	human		GRCh37 chr5: 8,706,641-8,742,651 , GRCh38.p12 chr5: 8,706,529-8,742,539	0
nsv6631082	copy number variation	194	nstd224	human		GRCh37 chr6: 67,017,494-67,044,618 , GRCh38.p12 chr6: 66,307,601-66,334,725	0
nsv6633430	copy number variation	152	nstd224	human		GRCh37 chr9: 24,505,147-24,518,795 , GRCh38.p12 chr9: 24,505,149-24,518,797	0
nsv6623939	copy number variation	1	nstd224	human		GRCh37 chr16: 84,576,287-84,947,677 , GRCh38.p12 chr16: 84,542,681-84,914,071	USP10, COTL1, 5 more genes
nsv6623220	copy number variation	151	nstd224	human		GRCh37 chr16: 34,489,371-34,724,788 , GRCh38.p12 chr16: 35,255,000-35,490,417	AGGF1P4, C2orf69P3, 21 more genes
nsv6625079	copy number variation	2	nstd224	human		GRCh37 chr1: 105,319,960-105,385,756 , GRCh38.p12 chr1: 104,777,338-104,843,134	0
nsv6626851	copy number variation	60	nstd224	human		GRCh37 chr21: 15,248,281-15,263,760 , GRCh38.p12 chr21: 13,875,960-13,891,439	0

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