MS21130 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
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
nsv908408	copy number variation	102	nstd71	human		NCBI36 chr17: 41,781,845-41,922,658 , GRCh37.p13 chr17: 44,426,089-44,566,775 , GRCh38.p12 chr17: 46,348,723-46,489,976	ARL17B, NSFP1
nsv884459	copy number variation	16	nstd71	human		NCBI36 chr6: 31,893,432-31,903,349 , GRCh37.p13 chr6: 31,785,453-31,795,370 , GRCh37.p13 chr6\|NT_167244.1: 3,100,214-3,110,134 , GRCh37.p13 chr6\|NT_167245.1: 3,071,040-3,080,957 , GRCh38.p12 chr6: 31,817,676-31,827,593 , GRCh38.p12 chr6\|NT_167244.2: 3,150,298-3,160,218 , GRCh38.p12 chr6\|NT_167245.2: 3,065,455-3,075,372	HSPA1A, HSPA1B
nsv898672	copy number variation	69	nstd71	human		NCBI36 chr12: 7,884,583-8,017,012 , GRCh37.p13 chr12: 7,993,316-8,125,745 , GRCh38.p12 chr12: 7,840,720-7,973,149	SLC2A3, LOC100130582, 3 more genes
nsv872402	copy number variation	12	nstd71	human		NCBI36 chr1: 147,710,728-147,872,275 , GRCh37.p13 chr1: 149,444,104-149,605,651 , GRCh38.p12 chr1: 120,852,223-120,942,334	PPIAL4A, LOC100996720, 2 more genes
nsv880476	copy number variation	2	nstd71	human		NCBI36 chr4: 190,858,764-191,138,111 , GRCh37.p13 chr4: 190,621,770-190,828,225 , GRCh38.p12 chr4: 189,700,616-189,979,962	FRG1-DT, LINC01596, 5 more genes
nsv881306	copy number variation	1	nstd71	human		NCBI36 chr4: 185,942,000-190,775,829 , GRCh37.p13 chr4: 185,705,006-190,538,835 , GRCh38.p12 chr4: 184,783,852-189,617,681	RNU7-192P, SNX25, 78 more genes
nsv895538	copy number variation	101	nstd71	human		NCBI36 chr10: 58,562,281-58,608,558 , GRCh37.p13 chr10: 58,892,275-58,938,552 , GRCh38.p12 chr10: 57,132,515-57,178,792	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
nsv870782	copy number variation	60	nstd71	human		NCBI36 chr1: 12,777,429-12,845,198 , GRCh37.p13 chr1: 12,854,842-12,922,611 , GRCh38.p12 chr1: 12,794,693-12,862,756 , GRCh38.p12 chr1\|NW_012132914.1: 1-44,269	HNRNPCL1, LINC01784, 4 more genes
nsv906437	copy number variation	30	nstd71	human		NCBI36 chr16: 32,470,417-32,511,911 , GRCh37.p13 chr16: 32,562,916-32,604,410 , GRCh38.p12 chr16: 32,551,595-32,593,089	0

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