OSC2059 AND nstd224 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv6632327	copy number variation	204	nstd224	human	GRCh37 chr8: 137,688,230-137,852,251 , GRCh38.p12 chr8: 136,675,987-136,840,008	LINC02055
nsv6626569	copy number variation	6	nstd224	human	GRCh37 chr20: 41,181,630-41,238,504 , GRCh38.p12 chr20: 42,552,990-42,609,864	PTPRT
nsv6620674	copy number variation	1	nstd224	human	GRCh37 chr10: 68,613,644-68,649,352 , GRCh38.p12 chr10: 66,853,886-66,889,594	CTNNA3
nsv6625579	copy number variation	6	nstd224	human	GRCh37 chr1: 110,215,178-110,233,147 , GRCh38.p12 chr1: 109,672,556-109,690,525	GSTM2, GSTM1
nsv6630049	copy number variation	1	nstd224	human	GRCh37 chr5: 129,469,043-129,545,263 , GRCh38.p12 chr5: 130,133,350-130,209,570	CHSY3, HSPA8P4
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
nsv6626678	copy number variation	1	nstd224	human	GRCh37 chr20: 18,849,570-18,909,558 , GRCh38.p12 chr20: 18,868,926-18,928,914	0
nsv6629428	copy number variation	9	nstd224	human	GRCh37 chr4: 25,970,163-25,983,887 , GRCh38.p12 chr4: 25,968,541-25,982,265	0
nsv6621457	copy number variation	226	nstd224	human	GRCh37 chr12: 31,266,287-31,406,907 , GRCh38.p12 chr12: 31,113,353-31,253,973 , GRCh38.p12 chr12\|NT_187587.1: 1,874-144,767	OVOS2, RPL13AP22, 6 more genes
nsv6630183	copy number variation	48	nstd224	human	GRCh37 chr4: 9,371,116-9,485,300 , GRCh38.p12 chr4: 9,369,390-9,483,653	OR7E84P, USP17L6P, 7 more genes

dbVar