OSC1989 AND nstd224 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv6624963	copy number variation	14	nstd224	human	GRCh37 chr19: 41,356,246-41,388,562 , GRCh38.p12 chr19: 40,850,341-40,882,657	CYP2A6, CYP2A7
nsv6627688	copy number variation	35	nstd224	human	GRCh37 chr2: 13,202,216-13,259,411 , GRCh38.p12 chr2: 13,062,091-13,119,286	LOC105373436, LOC105373484
nsv6620485	copy number variation	471	nstd224	human	GRCh37 chr10: 47,543,322-47,703,946 , GRCh38.p12 chr10: 46,172,086-46,332,710	AHCYP1, ANTXRL, 2 more genes
nsv6620467	copy number variation	5	nstd224	human	GRCh37 chr10: 46,965,747-47,047,517 , GRCh38.p12 chr10: 46,526,172-46,583,870	SYT15, SYT15-AS1, 1 more genes
nsv6629754	copy number variation	17	nstd224	human	GRCh37 chr4: 9,371,116-9,496,079 , GRCh38.p12 chr4: 9,369,390-9,494,435	OR7E85P, OR7E84P, 8 more genes
nsv6622412	copy number variation	59	nstd224	human	GRCh37 chr13: 70,744,882-70,767,093 , GRCh38.p12 chr13: 70,170,750-70,192,961	0
nsv6632195	copy number variation	32	nstd224	human	GRCh37 chr7: 76,432,653-76,639,871 , GRCh38.p12 chr7: 76,803,336-77,010,554	FDPSP7, DTX2P1-UPK3BP1-PMS2P11, 4 more genes