IS41883 AND nstd71 - dbVar - NCBI

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Items: 11

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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
nsv884822	copy number variation	2547	nstd71	human		NCBI36 chr6: 32,560,168-32,593,470 , GRCh37.p13 chr6: 32,452,190-32,485,492 , GRCh38.p12 chr6: 32,484,413-32,517,715	HLA-DRB5
nsv890775	copy number variation	26	nstd71	human		NCBI36 chr8: 39,356,825-39,457,081 , GRCh37.p13 chr8: 39,237,668-39,337,924 , GRCh38.p12 chr8: 39,380,149-39,480,405	ADAM5, ADAM3A
nsv881673	copy number variation	95	nstd71	human		NCBI36 chr5: 9,953,083-9,981,862 , GRCh37.p13 chr5: 9,900,083-9,928,862 , GRCh38.p12 chr5: 9,899,971-9,928,750	LOC107986405, LINC02112
nsv909473	copy number variation	1	nstd71	human		NCBI36 chr18: 22,909,233-23,046,073 , GRCh37.p13 chr18: 24,655,235-24,792,075 , GRCh38.p12 chr18: 27,075,271-27,212,111	CHST9,
nsv911369	copy number variation	219	nstd71	human		NCBI36 chr19: 20,404,485-20,520,617 , GRCh37.p13 chr19: 20,612,645-20,728,777 , GRCh37.p13 chr19\|NW_003571053.2: 347,092-463,224 , GRCh38.p12 chr19: 20,429,839-20,545,971	ZNF737, LOC105372316, 2 more genes
nsv903660	copy number variation	7	nstd71	human		NCBI36 chr15: 22,056,668-22,232,140 , GRCh37.p13 chr15: 24,505,575-24,681,047 , GRCh38.p12 chr15: 24,260,428-24,435,900	LOC105370733, LOC102725165, 1 more genes
nsv888268	copy number variation	1	nstd71	human		NCBI36 chr7: 63,348,722-63,398,516 , GRCh37.p13 chr7: 63,711,287-63,761,081 , GRCh38.p12 chr7: 64,250,909-64,300,703	VN1R39P, LOC105375323, 2 more genes
nsv886057	copy number variation	200	nstd71	human		NCBI36 chr6: 67,065,007-67,111,682 , GRCh37.p13 chr6: 67,008,286-67,054,961 , GRCh38.p12 chr6: 66,298,393-66,345,068	0
nsv884226	copy number variation	67	nstd71	human		NCBI36 chr6: 31,385,967-31,396,472 , GRCh37.p13 chr6: 31,277,988-31,288,493 , GRCh37.p13 chr6\|NT_167249.1: 2,611,726-2,622,207 , GRCh37.p13 chr6\|NT_167246.1: 2,624,814-2,631,393 , GRCh38.p12 chr6\|NT_167246.2: 2,619,194-2,625,775 , GRCh38.p12 chr6\|NT_167249.2: 2,612,428-2,622,909 , GRCh38.p12 chr6: 31,310,211-31,320,716	0
nsv901291	copy number variation	18	nstd71	human		NCBI36 chr14: 19,261,709-19,479,098 , GRCh37.p13 chr14: 20,191,869-20,409,258 , GRCh38.p12 chr14: 19,723,710-19,941,099	OR4N1P, LOC100421751, 11 more genes
nsv871157	copy number variation	1	nstd71	human		NCBI36 chr1: 13,036,311-13,328,755 , GRCh37.p13 chr1: 13,113,724-13,456,168 , GRCh38.p12 chr1\|NT_187517.1: 1-168,039	PRAMEF13, HNRNPCL4, 9 more genes

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