OSC4162 AND nstd224 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv6626599	copy number variation	1	nstd224	human	GRCh37 chr20: 5,791,066-5,842,094 , GRCh38.p12 chr20: 5,810,420-5,861,448	SHLD1
nsv6621722	copy number variation	15	nstd224	human	GRCh37 chr12: 57,342,188-57,376,840 , GRCh38.p12 chr12: 56,948,404-56,983,056	RDH16, LOC390332
nsv6632306	copy number variation	3	nstd224	human	GRCh37 chr8: 115,321,191-115,342,541 , GRCh38.p12 chr8: 114,308,962-114,330,312	LOC105375710, LOC100420746
nsv6630884	copy number variation	168	nstd224	human	GRCh37 chr5: 814,876-825,329 , GRCh38.p12 chr5: 814,761-825,214	ZDHHC11, SPCS2P3
nsv6629065	copy number variation	500	nstd224	human	GRCh37 chr3: 65,193,246-65,211,507 , GRCh38.p12 chr3: 65,207,571-65,225,832	0
nsv6623615	copy number variation	320	nstd224	human	GRCh37 chr16: 34,516,075-34,686,820 , GRCh38.p12 chr16: 35,281,704-35,452,449	AGGF1P4, FRG2IP, 14 more genes