IS37969 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
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
nsv889263	copy number variation	249	nstd71	human		NCBI36 chr7: 141,410,335-141,441,259 , GRCh37.p13 chr7\|NW_003571040.1: 206,017-236,941 , GRCh37.p13 chr7: 141,763,866-141,794,790 , GRCh38.p12 chr7: 142,064,066-142,094,990 , GRCh38.p12 chr7\|NT_187562.1: 25,946-56,870	MGAM
nsv882702	copy number variation	1	nstd71	human		NCBI36 chr5: 109,793,151-109,942,999 , GRCh37.p13 chr5: 109,765,252-109,915,100 , GRCh38.p12 chr5: 110,429,551-110,579,399	MIR548F3, TMEM232
nsv880300	copy number variation	1	nstd71	human		NCBI36 chr5: 12,857,565-12,950,742 , GRCh37.p13 chr5: 12,804,565-12,897,742 , GRCh38.p12 chr5: 12,804,453-12,897,630	LINC02220, LOC105374657, 1 more genes
nsv914684	copy number variation	27	nstd71	human		NCBI36 chr22: 23,991,725-24,113,704 , GRCh37.p13 chr22: 25,661,725-25,783,704 , GRCh38.p12 chr22: 25,265,758-25,387,737	LRP5L, IGLL3P, 2 more genes
nsv888859	copy number variation	19	nstd71	human		NCBI36 chr7: 101,921,012-102,121,342 , GRCh37.p13 chr7: 102,134,007-102,334,106 , GRCh38.p12 chr7: 102,493,560-102,693,659	RASA4DP, SPDYE2B, 7 more genes
nsv904023	copy number variation	257	nstd71	human		NCBI36 chr15: 32,487,589-32,625,184 , GRCh37.p13 chr15: 34,700,297-34,837,892 , GRCh38.p12 chr15: 34,408,096-34,545,691	LOC100422491, GOLGA8B, 5 more genes
nsv911409	copy number variation	1	nstd71	human		NCBI36 chr19: 20,618,710-20,793,016 , GRCh37.p13 chr19\|NW_003315962.1: 1-155,355 , GRCh37.p13 chr19: 20,845,947-21,001,176 , GRCh38.p12 chr19: 20,644,064-20,818,370 , GRCh38.p12 chr19\|NW_003315962.1: 1-155,355	ZNF66, VN1R79P, 4 more genes
nsv915172	copy number variation	84	nstd71	human		NCBI36 chr22: 21,047,055-21,075,525 , GRCh37.p13 chr22: 22,717,055-22,745,525 , GRCh38.p12 chr22\|NT_187629.1: 1-17,710 , GRCh38.p12 chr22: 22,362,695-22,391,157	IGLV7-46, IGLV1-44, 4 more genes
nsv902521	copy number variation	28	nstd71	human		NCBI36 chr14: 105,083,528-105,308,150 , GRCh37.p13 chr14\|NW_004166863.1: 209,313-433,935 , GRCh37.p13 chr14: 106,012,483-106,237,105 , GRCh38.p12 chr14: 105,546,146-105,770,768 , GRCh38.p12 chr14\|NT_187600.1: 13,144-238,537	MIR8071-1, IGHA1, 19 more genes
nsv894616	copy number variation	39	nstd71	human		NCBI36 chr9: 139,188,163-139,338,799 , GRCh37.p13 chr9: 140,068,342-140,218,978 , GRCh38.p12 chr9: 137,173,890-137,324,526	EXD3, TOR4A, 15 more genes
nsv914946	copy number variation	23	nstd71	human		NCBI36 chr22: 24,219,385-24,244,593 , GRCh37.p13 chr22: 25,889,385-25,914,593 , GRCh38.p12 chr22: 25,493,418-25,518,626	0

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