OSC8183 AND nstd224 - dbVar - NCBI

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6625689	copy number variation	1	nstd224	human		GRCh37 chr1: 187,296,703-187,348,378 , GRCh38.p12 chr1: 187,327,571-187,379,246	LINC01036
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
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
nsv6629306	copy number variation	49	nstd224	human		GRCh37 chr3: 75,447,252-75,563,370 , GRCh38.p12 chr3: 75,398,101-75,514,219	LINC02018, FAM86DP, 2 more genes
nsv6621100	copy number variation	1	nstd224	human		GRCh37 chr11: 48,387,275-48,925,223 , GRCh38.p12 chr11: 48,365,723-48,903,671	OR4C5, OR4C10P, 13 more genes
nsv6625349	copy number variation	3	nstd224	human		GRCh37 chr1: 12,832,317-13,634,781 , GRCh38.p12 chr1: 12,772,175-13,308,389	PRAMEF13, PRAMEF6, 30 more genes
nsv6627197	copy number variation	4	nstd224	human		GRCh37 chr22: 24,301,860-24,390,432 , GRCh38.p12 chr22\|NT_187633.1: 196,035-284,607	GSTT1, DDTL, 10 more genes
nsv6620131	copy number variation	3	nstd224	human		GRCh37 chr10: 42,501,173-42,521,825 , GRCh38.p12 chr10: 41,718,384-41,739,036	0
nsv6624084	copy number variation	158	nstd224	human		GRCh37 chr17: 44,179,983-44,353,222 , GRCh38.p12 chr17: 46,102,617-46,275,856 , GRCh38.p12 chr17\|NT_187663.1: 804,722-954,783	KANSL1, KANSL1-AS1, 5 more genes
nsv6623606	copy number variation	28	nstd224	human		GRCh37 chr16: 32,509,483-33,615,125 , GRCh38.p12 chr16: 32,498,162-33,812,658	IGHV3OR16-12, IGHV3OR16-8, 36 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
nsv6622360	copy number variation	81	nstd224	human		GRCh37 chr14: 20,198,662-20,416,499 , GRCh38.p12 chr14: 19,730,503-19,948,340	OR4K6P, OR4K5, 11 more genes
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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OSC8183 AND nstd224 (14)
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