OSC6863 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
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
nsv6630215	copy number variation	9	nstd224	human		GRCh37 chr5: 110,427,347-110,442,998 , GRCh38.p12 chr5: 111,091,649-111,107,299	WDR36
nsv6623349	copy number variation	17	nstd224	human		GRCh37 chr15: 87,828,560-87,866,035 , GRCh38.p12 chr15: 87,285,329-87,322,804	LOC107984735,
nsv6625115	copy number variation	1	nstd224	human		GRCh37 chr19: 41,355,544-41,387,798 , GRCh38.p12 chr19: 40,849,639-40,881,893	CYP2A7, CYP2A6
nsv6623654	copy number variation	84	nstd224	human		GRCh37 chr16: 32,509,483-33,772,866 , GRCh38.p12 chr16: 32,498,162-33,970,399	IGHV3OR16-11, LOC342443, 43 more genes
nsv6631082	copy number variation	194	nstd224	human		GRCh37 chr6: 67,017,494-67,044,618 , GRCh38.p12 chr6: 66,307,601-66,334,725	0
nsv6629772	copy number variation	1	nstd224	human		GRCh37 chr4: 70,264,026-70,672,152 , GRCh38.p12 chr4: 69,398,308-69,806,434	UGT2A1, UGT2B24P, 8 more genes
nsv6626893	copy number variation	2	nstd224	human		GRCh37 chr22: 17,055,569-17,289,118 , GRCh38.p12 chr22: 16,574,679-16,808,228	TPTEP1, VWFP1, 10 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

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OSC6863 AND nstd224 (13)
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