OSC8805 AND nstd224 - dbVar - NCBI

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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
nsv6631779	copy number variation	63	nstd224	human		GRCh37 chr7: 141,772,099-141,794,376 , GRCh38.p12 chr7: 142,072,299-142,094,576 , GRCh38.p12 chr7\|NT_187562.1: 34,179-56,456	MGAM
nsv6625091	copy number variation	291	nstd224	human		GRCh37 chr1: 110,228,505-110,241,385 , GRCh38.p12 chr1: 109,685,883-109,698,763	GSTM1
nsv6629198	copy number variation	20	nstd224	human		GRCh37 chr4: 161,953,637-161,997,950 , GRCh38.p12 chr4: 161,032,485-161,076,798	LOC105377514
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
nsv6625074	copy number variation	49	nstd224	human		GRCh37 chr1: 104,113,158-104,153,766 , GRCh38.p12 chr1: 103,570,536-103,611,144	ACTG1P4, AMY2B
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
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
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
nsv6623832	copy number variation	2	nstd224	human		GRCh37 chr17: 21,715,886-22,198,440 , GRCh38.p12 chr17: 22,189,280-22,699,113	UBBP4, LOC105371597, 21 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
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

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