OSC6162 AND nstd224 - dbVar - NCBI

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6626132	copy number variation	1	nstd224	human		GRCh37 chr1: 194,428,838-194,545,670 , GRCh38.p12 chr1: 194,459,708-194,576,540	RNU6-983P
nsv6629898	copy number variation	832	nstd224	human		GRCh37 chr4: 69,401,172-69,435,811 , GRCh38.p12 chr4: 68,535,454-68,570,093	UGT2B17
nsv6625728	copy number variation	1	nstd224	human		GRCh37 chr1: 201,628,990-201,644,752 , GRCh38.p12 chr1: 201,659,862-201,675,624	NAV1
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
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
nsv6624688	copy number variation	2	nstd224	human		GRCh37 chr19: 20,605,360-20,730,207 , GRCh38.p12 chr19: 20,422,554-20,547,401	BNIP3P23, LOC105372316, 3 more genes
nsv6625357	copy number variation	7	nstd224	human		GRCh37 chr1: 12,865,657-12,915,500 , GRCh38.p12 chr1: 12,805,521-12,855,646 , GRCh38.p12 chr1\|NW_012132914.1: 1-37,159	LINC01784, PRAMEF2, 3 more genes
nsv6623708	copy number variation	10	nstd224	human		GRCh37 chr16: 72,088,331-72,108,093 , GRCh38.p12 chr16: 72,054,432-72,074,194	HPR, TXNL4B, 1 more genes
nsv6627053	copy number variation	7	nstd224	human		GRCh37 chr22: 22,318,346-22,563,845 , GRCh38.p12 chr22: 21,963,974-22,209,454	IGLVI-70, IGLVI-56, 24 more genes
nsv6626927	copy number variation	2	nstd224	human		GRCh37 chr22: 24,302,603-24,390,432 , GRCh38.p12 chr22\|NT_187633.1: 196,778-284,607	GSTT2, DDTL, 10 more genes
nsv6622289	copy number variation	1	nstd224	human		GRCh37 chr14: 42,491,685-42,554,391 , GRCh38.p12 chr14: 42,022,482-42,085,188	0
nsv6620503	copy number variation	42	nstd224	human		GRCh37 chr10: 58,899,460-58,932,805 , GRCh38.p12 chr10: 57,139,700-57,173,045	0

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