IS41703 AND nstd71 - dbVar - NCBI

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv890816	copy number variation	21	nstd71	human		NCBI36 chr8: 39,421,344-39,497,557 , GRCh37.p13 chr8: 39,302,187-39,378,400 , GRCh38.p12 chr8: 39,444,668-39,520,881	ADAM3A
nsv888881	copy number variation	5	nstd71	human		NCBI36 chr7: 102,005,497-102,062,128 , GRCh37.p13 chr7: 102,218,400-102,274,889 , GRCh38.p12 chr7: 102,577,953-102,634,442	RASA4
nsv886284	copy number variation	1	nstd71	human		NCBI36 chr6: 79,039,487-79,086,086 , GRCh37.p13 chr6: 78,982,768-79,029,367 , GRCh38.p12 chr6: 78,273,051-78,319,650	LOC105377865
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
nsv909839	copy number variation	966	nstd71	human		NCBI36 chr18: 64,895,268-64,909,808 , GRCh37.p13 chr18: 66,744,288-66,758,828 , GRCh38.p12 chr18: 69,077,051-69,091,591	CCDC102B
nsv879318	copy number variation	371	nstd71	human		NCBI36 chr4: 69,085,989-69,179,871 , GRCh37.p13 chr4: 69,403,394-69,497,276 , GRCh38.p12 chr4: 68,537,676-68,631,558	LOC728807, UGT2B17, 2 more genes
nsv879389	copy number variation	2	nstd71	human		NCBI36 chr4: 70,072,336-70,164,518 , GRCh37.p13 chr4: 70,037,747-70,129,929 , GRCh38.p12 chr4: 69,172,029-69,264,211	UGT2B11, LOC100533845, 3 more genes
nsv911348	copy number variation	463	nstd71	human		NCBI36 chr19: 20,386,247-20,520,617 , GRCh37.p13 chr19\|NW_003571053.2: 329,860-463,224 , GRCh37.p13 chr19: 20,522,409-20,728,777 , GRCh38.p12 chr19: 20,411,600-20,545,971	BNIP3P23, LOC105372317, 4 more genes
nsv884554	copy number variation	1	nstd71	human		NCBI36 chr6: 32,057,331-32,089,979 , GRCh37.p13 chr6\|NT_167245.1: 3,234,933-3,267,584 , GRCh37.p13 chr6\|NT_167249.1: 3,282,062-3,314,711 , GRCh37.p13 chr6: 31,949,352-31,982,001 , GRCh38.p12 chr6: 31,981,575-32,014,224 , GRCh38.p12 chr6\|NT_167245.2: 3,229,348-3,261,999 , GRCh38.p12 chr6\|NT_167249.2: 3,282,764-3,315,413	C4B_2, TNXA, 5 more genes
nsv907876	copy number variation	8	nstd71	human		NCBI36 chr17: 20,347,741-20,490,842 , GRCh37.p13 chr17: 20,407,149-20,550,250 , GRCh38.p12 chr17: 20,503,836-20,646,937	LOC105371580, KRT17P6, 12 more genes
nsv899523	copy number variation	1	nstd71	human		NCBI36 chr12: 110,648,029-110,806,867 , GRCh37.p13 chr12: 112,163,646-112,322,484 , GRCh38.p12 chr12: 111,725,842-111,884,680	MAPKAPK5, MIR6761, 4 more genes
nsv882130	copy number variation	76	nstd71	human		NCBI36 chr5: 70,311,476-70,434,279 , GRCh37.p13 chr5: 70,275,720-70,398,523 , GRCh38.p12 chr5: 70,979,893-71,102,696	NAIPP4, SNORD13B-2, 4 more genes

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