OSC8185 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
nsv6631879	copy number variation	1	nstd224	human		GRCh37 chr7: 3,709,800-3,765,004 , GRCh38.p12 chr7: 3,670,168-3,725,372	SDK1
nsv6631156	copy number variation	1	nstd224	human		GRCh37 chr6: 31,015,182-31,040,415 , GRCh38.p12 chr6: 31,047,405-31,072,638	HCG22
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
nsv6634108	copy number variation	11	nstd224	human		GRCh37 chrX: 94,314,391-94,375,989 , GRCh38.p12 chrX: 95,059,392-95,120,990	MIR548M
nsv6630661	copy number variation	3	nstd224	human		GRCh37 chr6: 125,535,917-125,585,733 , GRCh38.p12 chr6: 125,214,771-125,264,587	TPD52L1
nsv6630433	copy number variation	28	nstd224	human		GRCh37 chr5: 700,560-785,864 , GRCh38.p12 chr5: 700,445-785,749	ZDHHC11B, TPPP
nsv6623058	copy number variation	3	nstd224	human		GRCh37 chr15: 24,578,496-24,760,674 , GRCh38.p12 chr15: 24,333,349-24,515,527	LOC102723749, LOC105370733, 2 more genes
nsv6630124	copy number variation	1	nstd224	human		GRCh37 chr5: 17,483,926-17,509,888 , GRCh38.p12 chr5: 17,483,817-17,509,779	H3Y2, TAF11L2, 2 more genes
nsv6631241	copy number variation	11	nstd224	human		GRCh37 chr6: 29,917,195-29,937,833 , GRCh38.p12 chr6: 29,949,418-29,970,056	HLA-W, HCG4P4, 1 more genes
nsv6624230	copy number variation	9	nstd224	human		GRCh37 chr17: 34,438,753-34,465,860 , GRCh38.p12 chr17: 36,111,360-36,138,480 , GRCh38.p12 chr17\|NT_187661.1: 65,457-92,577 , GRCh38.p12 chr17\|NT_187614.1: 346,281-373,388	LOC107985055, LOC101927369, 1 more genes
nsv6626576	copy number variation	1	nstd224	human		GRCh37 chr20: 46,469,317-46,660,391 , GRCh38.p12 chr20: 47,840,573-48,031,647	LINC01522, RNU7-92P, 8 more genes

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OSC8185 AND nstd224 (12)
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