OSC4710 AND nstd224 - dbVar - NCBI

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Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6630256	copy number variation	50	nstd224	human		GRCh37 chr5: 104,436,002-104,494,583 , GRCh38.p12 chr5: 105,100,301-105,158,882	RAB9BP1
nsv6627584	copy number variation	1	nstd224	human		GRCh37 chr2: 242,352,768-242,380,873 , GRCh38.p12 chr2: 241,413,353-241,441,458	FARP2
nsv6630982	copy number variation	2	nstd224	human		GRCh37 chr6: 32,487,242-32,501,715 , GRCh38.p12 chr6: 32,519,465-32,533,938	HLA-DRB5
nsv6632506	copy number variation	7	nstd224	human		GRCh37 chr8: 144,942,796-145,006,576 , GRCh38.p12 chr8: 143,868,628-143,932,408	PLEC, EPPK1
nsv6627688	copy number variation	35	nstd224	human		GRCh37 chr2: 13,202,216-13,259,411 , GRCh38.p12 chr2: 13,062,091-13,119,286	LOC105373436, LOC105373484
nsv6628875	copy number variation	412	nstd224	human		GRCh37 chr3: 75,453,294-75,554,281 , GRCh38.p12 chr3: 75,404,143-75,505,130	ENPP7P2, LINC02018, 2 more genes
nsv6634059	copy number variation	43	nstd224	human		GRCh37 chrX: 47,911,871-47,970,727 , GRCh38.p12 chrX: 48,052,481-48,111,343	SSX6P, ZNF630, 1 more genes
nsv6633226	copy number variation	78	nstd224	human		GRCh37 chr9: 140,166,981-140,196,334 , GRCh38.p12 chr9: 137,272,529-137,301,882	NRARP, TOR4A, 1 more genes
nsv6623137	copy number variation	5	nstd224	human		GRCh37 chr15: 65,369,242-65,385,511 , GRCh38.p12 chr15: 65,076,904-65,093,173	RASL12, KBTBD13, 1 more genes
nsv6623855	copy number variation	73	nstd224	human		GRCh37 chr17: 44,169,808-44,293,020 , GRCh38.p12 chr17: 46,092,442-46,215,654 , GRCh38.p12 chr17\|NT_187663.1: 794,550-917,827	KANSL1, KANSL1-AS1, 1 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

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