IS39386 AND nstd71 - dbVar - NCBI

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Items: 10

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Number of Variants: 10

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv882725	copy number variation	7	nstd71	human		NCBI36 chr5: 112,974,949-113,017,800 , GRCh37.p13 chr5: 112,947,050-112,989,901 , GRCh38.p12 chr5: 113,611,353-113,654,204	LOC107986441
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
nsv898379	copy number variation	14	nstd71	human		NCBI36 chr11: 107,154,236-107,178,510 , GRCh37.p13 chr11: 107,649,026-107,673,300 , GRCh38.p12 chr11: 107,778,300-107,802,574	SLC35F2
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
nsv895309	copy number variation	6	nstd71	human		NCBI36 chr10: 47,093,844-47,197,303 , GRCh37.p13 chr10: 47,623,838-47,689,665 , GRCh37.p13 chr10\|NW_003871068.1: 523,717-589,544 , GRCh38.p12 chr10: 46,252,602-46,356,071	LOC105378577, AGAP14P, 2 more genes
nsv873943	copy number variation	269	nstd71	human		NCBI36 chr2: 41,083,802-41,109,046 , GRCh37.p13 chr2: 41,230,298-41,255,542 , GRCh38.p12 chr2: 41,003,158-41,028,402	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
nsv871980	copy number variation	39	nstd71	human		NCBI36 chr1: 103,930,296-104,107,839 , GRCh37.p13 chr1: 104,128,773-104,306,316 , GRCh38.p12 chr1: 103,586,151-103,763,694	AMY1B, AMY2A, 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
nsv902568	copy number variation	7	nstd71	human		NCBI36 chr14: 105,143,515-105,308,150 , GRCh37.p13 chr14: 106,072,470-106,237,105 , GRCh37.p13 chr14\|NW_004166863.1: 269,300-433,935 , GRCh38.p12 chr14\|NT_187600.1: 73,902-238,537 , GRCh38.p12 chr14: 105,606,133-105,770,768	IGHEP1, IGHG2, 14 more genes

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