IS33622 AND nstd71 - dbVar - NCBI

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Items: 12

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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
nsv888893	copy number variation	13	nstd71	human		NCBI36 chr7: 102,022,918-102,062,128 , GRCh37.p13 chr7: 102,235,849-102,274,889 , GRCh38.p12 chr7: 102,595,402-102,634,442	RASA4
nsv890754	copy number variation	920	nstd71	human		NCBI36 chr8: 39,350,791-39,509,376 , GRCh37.p13 chr8: 39,231,634-39,390,219 , GRCh38.p12 chr8: 39,374,115-39,532,700	ADAM5, ADAM3A
nsv880244	copy number variation	1	nstd71	human		NCBI36 chr4: 148,983,702-149,139,539 , GRCh37.p13 chr4: 148,764,252-148,920,089 , GRCh38.p12 chr4: 147,843,101-147,998,938	RFPL4AP4, ARHGAP10
nsv911995	copy number variation	2	nstd71	human		NCBI36 chr19: 48,157,656-48,253,562 , GRCh37.p13 chr19: 43,465,816-43,561,722 , GRCh38.p12 chr19: 42,961,664-43,057,570	CEACAMP8, PSG11
nsv911912	copy number variation	43	nstd71	human		NCBI36 chr19: 48,060,801-48,160,500 , GRCh37.p13 chr19: 43,368,961-43,468,660 , GRCh38.p12 chr19: 42,864,809-42,964,508	CEACAMP7, PSG1, 2 more genes
nsv902691	copy number variation	2	nstd71	human		NCBI36 chr15: 18,708,208-18,922,271 , GRCh37.p13 chr15: 20,448,194-20,662,257 , GRCh38.p12 chr15: 20,242,941-20,457,004	RHPN2P1, CHEK2P2, 1 more genes
nsv874293	copy number variation	1	nstd71	human		NCBI36 chr2: 74,756,098-74,824,429 , GRCh37.p13 chr2: 74,902,590-74,970,921 , GRCh38.p12 chr2: 74,675,463-74,743,794	SEMA4F, , 1 more genes
nsv903100	copy number variation	7	nstd71	human		NCBI36 chr15: 19,359,417-19,556,128 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr15: 20,924,655-21,498,353	MIR3118-3, BCAR1P2, 23 more genes
nsv890264	copy number variation	52	nstd71	human		NCBI36 chr8: 7,575,048-7,840,086 , GRCh37.p13 chr8: 7,537,638-7,802,676 , GRCh38.p12 chr8: 7,680,116-7,945,154 , GRCh38.p12 chr8\|NW_018654717.1: 5,303,324-5,513,617	FAM90A16, DEFB106A, 40 more genes
nsv890161	copy number variation	90	nstd71	human		NCBI36 chr8: 7,242,915-7,459,302 , GRCh37.p13 chr8: 7,255,505-7,471,892 , GRCh38.p12 chr8\|NT_187570.1: 81,014-297,473 , GRCh38.p12 chr8: 7,397,983-7,614,370	FAM90A22, FAM90A21P, 17 more genes
nsv874298	copy number variation	1	nstd71	human		NCBI36 chr2: 74,905,331-75,134,562 , GRCh37.p13 chr2: 75,051,823-75,281,054 , GRCh38.p12 chr2: 74,824,696-75,053,927	HK2, LINC01293, 4 more genes
nsv914480	copy number variation	3	nstd71	human		NCBI36 chr22: 20,630,941-20,910,314 , GRCh37.p13 chr22: 22,300,941-22,580,314 , GRCh38.p12 chr22: 21,946,569-22,225,921	IGLVIV-59, IGLV4-69, 28 more genes

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