IS35973 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
nsv884832	copy number variation	107	nstd71	human		NCBI36 chr6: 32,560,168-32,601,256 , GRCh37.p13 chr6: 32,452,190-32,493,278 , GRCh38.p12 chr6: 32,484,413-32,525,501	HLA-DRB5
nsv889950	copy number variation	1	nstd71	human		NCBI36 chr8: 4,270,026-4,308,064 , GRCh37.p13 chr8: 4,282,618-4,320,656 , GRCh38.p12 chr8: 4,425,096-4,463,134	CSMD1
nsv897391	copy number variation	1	nstd71	human		NCBI36 chr11: 48,722,143-48,917,273 , GRCh37.p13 chr11: 48,765,567-48,960,697 , GRCh38.p12 chr11: 48,744,015-48,939,145	LOC100420449, ANKRD33BP2
nsv872992	copy number variation	87	nstd71	human		NCBI36 chr1: 194,977,690-195,089,653 , GRCh37.p13 chr1: 196,711,067-196,823,030 , GRCh38.p12 chr1: 196,741,937-196,853,900	LOC100996886, CFHR3, 2 more genes
nsv898107	copy number variation	2	nstd71	human		NCBI36 chr11: 89,232,539-89,259,348 , GRCh37.p13 chr11: 89,592,891-89,619,700 , GRCh38.p12 chr11: 89,859,723-89,886,532	ANKRD33BP8, TRIM64B, 1 more genes
nsv879254	copy number variation	538	nstd71	human		NCBI36 chr4: 69,047,457-69,179,871 , GRCh37.p13 chr4: 69,364,862-69,497,276 , GRCh38.p12 chr4: 68,499,144-68,631,558	LOC728807, UGT2B29P, 3 more genes
nsv889750	copy number variation	1	nstd71	human		NCBI36 chr8: 2,003,460-2,133,500 , GRCh37.p13 chr8: 2,016,053-2,146,093 , GRCh37.p13 chr8\|NW_003571042.1: 50,664-180,704 , GRCh38.p12 chr8\|NT_187576.1: 251,263-381,303 , GRCh38.p12 chr8: 2,067,934-2,198,540	LOC105377781, MYOM2, 2 more genes
nsv893461	copy number variation	3	nstd71	human		NCBI36 chr9: 75,766,064-75,921,222 , GRCh37.p13 chr9: 76,576,244-76,731,402 , GRCh38.p12 chr9: 73,961,328-74,116,486	0
nsv889109	copy number variation	134	nstd71	human		NCBI36 chr7: 118,855,366-118,964,906 , GRCh37.p13 chr7: 119,068,130-119,177,670 , GRCh38.p12 chr7: 119,428,076-119,537,616	0
nsv884228	copy number variation	228	nstd71	human		NCBI36 chr6: 31,385,967-31,398,785 , GRCh37.p13 chr6\|NT_167249.1: 2,611,726-2,624,528 , GRCh37.p13 chr6\|NT_167246.1: 2,624,814-2,631,393 , GRCh37.p13 chr6: 31,277,988-31,290,806 , GRCh38.p12 chr6: 31,310,211-31,323,029 , GRCh38.p12 chr6\|NT_167246.2: 2,619,194-2,625,775 , GRCh38.p12 chr6\|NT_167249.2: 2,612,428-2,625,230	0
nsv901208	copy number variation	9	nstd71	human		NCBI36 chr14: 19,166,663-19,486,339 , GRCh37.p13 chr14: 20,096,940-20,416,499 , GRCh38.p12 chr14: 19,628,664-19,948,340	ARHGAP42P4, LOC100420171, 18 more genes

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