OSC6998 AND nstd224 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
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
nsv6632127	copy number variation	2	nstd224	human	GRCh37 chr7: 3,373,782-3,492,992 , GRCh38.p12 chr7: 3,334,150-3,453,360	SDK1, RPL21P72
nsv6623651	copy number variation	160	nstd224	human	GRCh37 chr16: 32,509,483-32,650,542 , GRCh38.p12 chr16: 32,498,162-32,639,221	FAM153DP, LOC107984013
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
nsv6631711	copy number variation	2	nstd224	human	GRCh37 chr6: 95,453,181-95,531,813 , GRCh38.p12 chr6: 94,743,463-94,822,095	0
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
nsv6622620	copy number variation	10	nstd224	human	GRCh37 chr15: 22,759,530-23,279,684 , GRCh38.p12 chr15: 22,593,412-23,113,538	TUBGCP5, ELMO2P1, 13 more genes
nsv6623614	copy number variation	36	nstd224	human	GRCh37 chr16: 34,489,371-34,740,580 , GRCh38.p12 chr16: 35,255,000-35,506,209	LINC01566, AGGF1P9, 23 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
nsv6624783	copy number variation	32	nstd224	human	GRCh37 chr19: 53,522,100-53,542,566 , GRCh38.p12 chr19: 53,018,847-53,039,313	0

dbVar