M2296 AND nstd157 - dbVar - NCBI

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3318012	copy number variation	1	nstd157	human		GRCh37 chr3: 129,959,468-129,971,890 , GRCh38.p12 chr3: 130,240,625-130,253,047	COL6A4P2
nsv3317365	copy number variation	1	nstd157	human		GRCh37 chr2: 55,324,500-55,335,045 , GRCh38.p12 chr2: 55,097,364-55,107,909	RTN4
nsv3318414	copy number variation	12	nstd157	human		GRCh37 chr15: 61,687,640-61,698,179 , GRCh38.p12 chr15: 61,395,441-61,405,980	LOC105370847
nsv3318914	copy number variation	27	nstd157	human		GRCh37 chr20: 52,647,631-52,656,535 , GRCh38.p12 chr20: 54,031,092-54,039,996	BCAS1
nsv3317836	copy number variation	19	nstd157	human		GRCh37 chr18: 67,208,806-67,217,271 , GRCh38.p12 chr18: 69,541,570-69,550,035	DOK6
nsv3318848	copy number variation	11	nstd157	human		GRCh37 chr11: 93,020,527-93,028,940 , GRCh38.p12 chr11: 93,287,361-93,295,774	SLC36A4
nsv3317201	copy number variation	1	nstd157	human		GRCh37 chr10: 135,074,921-135,082,346 , GRCh38.p12 chr10: 133,261,417-133,268,842	ADAM8
nsv3317660	copy number variation	4	nstd157	human		GRCh38.p12 chr6: 8,926,462-8,932,063 , GRCh37 chr6: 8,926,695-8,932,296	, LOC112267952
nsv3317846	copy number variation	16	nstd157	human		GRCh38.p12 chr9: 133,071,778-133,082,065 , GRCh37 chr9: 135,947,165-135,957,452	CEL, CELP
nsv3318128	copy number variation	5	nstd157	human		GRCh38.p12 chr10: 27,318,130-27,416,926 , GRCh37 chr10: 27,607,059-27,705,855 , GRCh38.p12 chr10\|NW_003315934.1: 79,776-178,572	PTCHD3, FAM210CP, 4 more genes
nsv3317287	copy number variation	1	nstd157	human		GRCh37 chr3: 7,878,423-7,922,313 , GRCh38.p12 chr3: 7,836,736-7,880,626	0
nsv3317733	copy number variation	4	nstd157	human		GRCh37 chr6: 76,243,490-76,265,724 , GRCh38.p12 chr6: 75,533,774-75,556,008	0
nsv3318478	copy number variation	26	nstd157	human		GRCh37 chr7: 62,149,006-62,162,385 , GRCh38.p12 chr7: 62,688,628-62,702,007	0
nsv3318502	copy number variation	31	nstd157	human		GRCh37 chr9: 78,004,378-78,011,616 , GRCh38.p12 chr9: 75,389,462-75,396,700	0
nsv3318389	copy number variation	4	nstd157	human		GRCh38.p12 chr8: 26,476,982-26,485,915 , GRCh37 chr8: 26,334,498-26,343,431	0

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