OSC0185 AND nstd224 - dbVar - NCBI

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Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6624916	copy number variation	40	nstd224	human		GRCh37 chr19: 41,356,310-41,386,033 , GRCh38.p12 chr19: 40,850,405-40,880,128	CYP2A6, CYP2A7
nsv6625720	copy number variation	20	nstd224	human		GRCh37 chr1: 196,759,317-196,887,530 , GRCh38.p12 chr1: 196,790,187-196,918,400	CFHR3, CFHR4, 3 more genes
nsv6622617	copy number variation	2	nstd224	human		GRCh37 chr15: 22,369,360-22,416,081 , GRCh38.p12 chr15: 22,081,409-22,128,130	OR4N3P, OR4M2-OT1, 2 more genes
nsv6622683	copy number variation	1	nstd224	human		GRCh37 chr14: 74,028,117-74,062,222 , GRCh38.p12 chr14: 73,561,413-73,595,518	ACOT2, ACOT4, 2 more genes
nsv6626302	copy number variation	1	nstd224	human		GRCh37 chr20: 1,002,656-1,187,586 , GRCh38.p12 chr20: 1,022,013-1,206,942	ACTG1P3, PSMF1, 3 more genes
nsv6626666	copy number variation	3	nstd224	human		GRCh37 chr22: 18,892,575-18,996,565 , GRCh38.p12 chr22: 18,905,062-19,009,052	DGCR5, PRODH, 1 more genes
nsv6633891	copy number variation	1	nstd224	human		GRCh37 chrX: 6,497,085-8,114,085 , GRCh38.p12 chrX: 6,579,044-8,146,044	STS, PUDP, 7 more genes
nsv6632275	copy number variation	68	nstd224	human		GRCh37 chr7: 8,838,717-8,855,423 , GRCh38.p12 chr7: 8,799,087-8,815,793	0
nsv6628177	copy number variation	68	nstd224	human		GRCh37 chr2: 90,002,742-90,229,318 , GRCh38.p12 chr2: 89,963,932-90,190,466	IGKV6D-41, IGKV3D-15, 19 more genes
nsv6625059	copy number variation	14	nstd224	human		GRCh37 chr19: 6,896,471-7,103,542 , GRCh38.p12 chr19: 6,896,460-7,103,531	ZNF557, MBD3L5, 9 more genes
nsv6621911	copy number variation	1	nstd224	human		GRCh37 chr13: 111,683,466-111,731,424 , GRCh38.p12 chr13: 111,031,119-111,079,077	0

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