SP52634 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
nsv894742	copy number variation	1	nstd71	human		NCBI36 chr10: 1,696,725-1,745,177 , GRCh37.p13 chr10: 1,706,725-1,755,177 , GRCh38.p12 chr10: 1,664,531-1,712,983	ADARB2
nsv901814	copy number variation	288	nstd71	human		NCBI36 chr14: 43,558,217-43,606,201 , GRCh37.p13 chr14: 44,488,467-44,536,451 , GRCh38.p12 chr14: 44,019,264-44,067,248	LINC02307
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
nsv894737	copy number variation	1	nstd71	human		NCBI36 chr10: 1,550,338-1,682,796 , GRCh37.p13 chr10: 1,560,338-1,692,796 , GRCh38.p12 chr10: 1,518,143-1,650,601	ADARB2, ADARB2-AS1
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
nsv894746	copy number variation	1	nstd71	human		NCBI36 chr10: 1,962,657-2,139,120 , GRCh37.p13 chr10: 1,972,657-2,149,120 , GRCh38.p12 chr10: 1,930,463-2,106,926	LINC00700, RNU6-889P, 2 more genes
nsv898487	copy number variation	1	nstd71	human		NCBI36 chr11: 133,665,264-133,715,739 , GRCh37.p13 chr11: 134,160,054-134,210,529 , GRCh38.p12 chr11: 134,290,160-134,340,635	GLB1L2, LOC100421417, 1 more genes
nsv884359	copy number variation	12	nstd71	human		NCBI36 chr6: 31,467,172-31,562,344 , GRCh37.p13 chr6\|NT_167249.1: 2,692,980-2,755,239 , GRCh37.p13 chr6: 31,359,193-31,454,365 , GRCh38.p12 chr6\|NT_167249.2: 2,693,682-2,755,941 , GRCh38.p12 chr6: 31,391,416-31,486,588	MICA, LINC01149, 5 more genes
nsv871622	copy number variation	7	nstd71	human		NCBI36 chr1: 12,771,679-12,841,261 , GRCh37.p13 chr1: 12,849,092-12,918,674 , GRCh38.p12 chr1: 12,788,951-12,858,819 , GRCh38.p12 chr1\|NW_012132914.1: 1-40,332	LINC01784, PRAMEF2, 4 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
nsv903315	copy number variation	38	nstd71	human		NCBI36 chr15: 19,788,495-20,203,694 , GRCh37.p13 chr15: 22,287,131-22,652,330 , GRCh38.p12 chr15: 21,999,180-22,308,242	LOC107984743, OR4M2, 17 more genes

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SP52634 AND nstd71 (13)
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