SP52872 AND nstd71 - dbVar - NCBI

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Items: 18

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv898147	copy number variation	1	nstd71	human		NCBI36 chr11: 89,745,017-89,865,187 , GRCh37.p13 chr11: 90,105,369-90,225,539 , GRCh38.p12 chr11: 90,372,201-90,492,371	DISC1FP1
nsv874982	copy number variation	1	nstd71	human		NCBI36 chr2: 122,892,792-122,926,814 , GRCh37.p13 chr2: 123,176,322-123,210,344 , GRCh38.p12 chr2: 122,418,746-122,452,768	LOC105373592
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
nsv888900	copy number variation	27	nstd71	human		NCBI36 chr7: 102,032,517-102,062,128 , GRCh37.p13 chr7: 102,245,449-102,274,889 , GRCh38.p12 chr7: 102,605,002-102,634,442	RASA4
nsv885334	copy number variation	36	nstd71	human		NCBI36 chr6: 32,632,659-32,647,375 , GRCh37.p13 chr6: 32,524,681-32,539,397 , GRCh38.p12 chr6: 32,556,904-32,571,620	HLA-DRB6
nsv893231	copy number variation	140	nstd71	human		NCBI36 chr9: 43,594,114-43,641,682 , GRCh37.p13 chr9: 43,654,118-43,701,686 , GRCh38.p12 chr9: 42,112,703-42,160,271	CNTNAP3B
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
nsv893276	copy number variation	6	nstd71	human		NCBI36 chr9: 43,616,717-43,730,292 , GRCh37.p13 chr9: 43,676,721-43,790,296 , GRCh38.p12 chr9: 42,024,093-42,137,668	LOC100420440, CNTNAP3B
nsv878504	copy number variation	1	nstd71	human		NCBI36 chr4: 3,613,397-3,704,693 , GRCh37.p13 chr4: 3,643,599-3,734,895 , GRCh38.p12 chr4: 3,641,872-3,733,168	LINC02171, LOC105374357
nsv885453	copy number variation	7	nstd71	human		NCBI36 chr6: 32,650,112-32,668,837 , GRCh37.p13 chr6: 32,542,134-32,560,859 , GRCh38.p12 chr6: 32,574,357-32,593,082	RNU1-152P, HLA-DRB1
nsv879323	copy number variation	137	nstd71	human		NCBI36 chr4: 69,087,412-69,179,871 , GRCh37.p13 chr4: 69,404,817-69,497,276 , GRCh38.p12 chr4: 68,539,099-68,631,558	LOC100422402, LOC100132651, 2 more genes
nsv871196	copy number variation	88	nstd71	human		NCBI36 chr1: 12,777,429-12,810,136 , GRCh37.p13 chr1: 12,854,842-12,887,549 , GRCh38.p12 chr1: 12,794,693-12,827,690	PRAMEF11, PRAMEF1, 1 more genes
nsv886993	copy number variation	1	nstd71	human		NCBI36 chr6: 168,927,421-169,104,797 , GRCh37.p13 chr6: 169,185,496-169,362,872 , GRCh37.p13 chr6\|NW_004166862.1: 1-187,824 , GRCh38.p12 chr6: 168,785,401-168,962,777 , GRCh38.p12 chr6\|NW_004166862.2: 1-185,823	LOC105378146, LOC105378144, 2 more genes
nsv908355	copy number variation	1	nstd71	human		NCBI36 chr17: 41,771,015-41,902,289 , GRCh37.p13 chr17: 44,415,257-44,546,973 , GRCh38.p12 chr17: 46,337,891-46,469,607	LRRC37A, , 2 more genes
nsv874634	copy number variation	114	nstd71	human		NCBI36 chr2: 89,721,421-89,911,010 , GRCh37.p13 chr2: 90,084,116-90,273,705 , GRCh38.p12 chr2: 90,045,284-90,234,838	IGKV3D-15, IGKV1D-16, 14 more genes
nsv892462	copy number variation	10	nstd71	human		NCBI36 chr9: 11,926,706-12,000,374 , GRCh37.p13 chr9: 11,936,706-12,010,374 , GRCh38.p12 chr9: 11,936,706-12,010,374	0
nsv906453	copy number variation	2	nstd71	human		NCBI36 chr16: 32,472,584-32,511,911 , GRCh37.p13 chr16: 32,565,083-32,604,410 , GRCh38.p12 chr16: 32,553,762-32,593,089	0
nsv895223	copy number variation	61	nstd71	human		NCBI36 chr10: 46,830,464-47,129,146 , GRCh37.p13 chr10: 47,410,458-47,659,140 , GRCh38.p12 chr: NaN-NaN	0

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SP52872 AND nstd71 (19)
dbVar
9517[top bioproject] NOT 13836[uid] (753)
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