OSC7585 AND nstd224 - dbVar - NCBI

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6632493	copy number variation	72	nstd224	human		GRCh37 chr8: 137,688,230-137,855,721 , GRCh38.p12 chr8: 136,675,987-136,843,478	LINC02055
nsv6629898	copy number variation	832	nstd224	human		GRCh37 chr4: 69,401,172-69,435,811 , GRCh38.p12 chr4: 68,535,454-68,570,093	UGT2B17
nsv6630069	copy number variation	1	nstd224	human		GRCh37 chr5: 157,803,588-157,814,498 , GRCh38.p12 chr5: 158,376,580-158,387,490	LINC02227
nsv6625487	copy number variation	38	nstd224	human		GRCh37 chr1: 110,228,436-110,243,335 , GRCh38.p12 chr1: 109,685,814-109,700,713	GSTM1
nsv6630790	copy number variation	26	nstd224	human		GRCh37 chr5: 700,560-777,854 , GRCh38.p12 chr5: 700,445-777,739	TPPP, ZDHHC11B
nsv6624500	copy number variation	8	nstd224	human		GRCh37 chr17: 61,955,076-61,977,248 , GRCh38.p12 chr17: 63,877,716-63,899,888	CSH1, GH2
nsv6628596	copy number variation	1	nstd224	human		GRCh37 chr3: 40,414,099-40,468,053 , GRCh38.p12 chr3: 40,372,608-40,426,562	ENTPD3-AS1, ENTPD3
nsv6624685	copy number variation	256	nstd224	human		GRCh37 chr19: 20,605,360-20,700,135 , GRCh38.p12 chr19: 20,422,554-20,517,329	BNIP3P23, LOC105372317, 2 more genes
nsv6627380	copy number variation	480	nstd224	human		GRCh37 chr22: 24,374,253-24,390,432 , GRCh38.p12 chr22\|NT_187633.1: 268,428-284,607	GSTTP2, GSTT1-AS1, 2 more genes
nsv6628919	copy number variation	30	nstd224	human		GRCh37 chr3: 175,893,644-175,914,118 , GRCh38.p12 chr3: 176,175,856-176,196,330 , GRCh38.p12 chr3\|NW_019805488.1: 60,367-80,841	0
nsv6630940	copy number variation	45	nstd224	human		GRCh37 chr6: 168,344,728-168,597,599 , GRCh38.p12 chr6: 167,944,048-168,196,919	KIF25, AFDN, 5 more genes
nsv6622361	copy number variation	75	nstd224	human		GRCh37 chr14: 20,198,662-20,416,848 , GRCh38.p12 chr14: 19,730,503-19,948,689	OR4K6P, OR4K5, 11 more genes
nsv6627895	copy number variation	12	nstd224	human		GRCh37 chr2: 57,402,202-57,455,549 , GRCh38.p12 chr2: 57,175,067-57,228,414	0
nsv6624897	copy number variation	2	nstd224	human		GRCh37 chr19: 40,666,981-40,681,387 , GRCh38.p12 chr19: 40,161,074-40,175,480	0

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