SP50694 AND nstd71 - dbVar - NCBI

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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
nsv899063	copy number variation	1	nstd71	human		NCBI36 chr12: 46,951,256-47,000,035 , GRCh37.p13 chr12: 48,664,989-48,713,768 , GRCh38.p12 chr12: 48,271,206-48,319,985	LOC105369753
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
nsv909839	copy number variation	966	nstd71	human		NCBI36 chr18: 64,895,268-64,909,808 , GRCh37.p13 chr18: 66,744,288-66,758,828 , GRCh38.p12 chr18: 69,077,051-69,091,591	CCDC102B
nsv898536	copy number variation	5	nstd71	human		NCBI36 chr11: 134,117,862-134,140,452 , GRCh37.p13 chr11: 134,612,652-134,635,242 , GRCh38.p12 chr11: 134,742,758-134,765,348	LINC02714
nsv879310	copy number variation	1929	nstd71	human		NCBI36 chr4: 69,076,346-69,179,871 , GRCh37.p13 chr4: 69,393,751-69,497,276 , GRCh38.p12 chr4: 68,528,033-68,631,558	LOC100422402, LOC100132651, 2 more genes
nsv883510	copy number variation	2	nstd71	human		NCBI36 chr6: 27,658,691-27,838,043 , GRCh37.p13 chr6: 27,550,712-27,730,064 , GRCh38.p12 chr6: 27,582,933-27,762,285	TRL-CAA2-1, TRV-AAC4-1, 21 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
nsv906397	copy number variation	1	nstd71	human		NCBI36 chr16: 32,469,040-32,511,911 , GRCh37.p13 chr16: 32,561,539-32,604,410 , GRCh38.p12 chr16: 32,550,218-32,593,089	0
nsv876893	copy number variation	298	nstd71	human		NCBI36 chr3: 65,159,939-65,190,844 , GRCh37.p13 chr3: 65,184,899-65,215,804 , GRCh38.p12 chr3: 65,199,224-65,230,129	0
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

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SP50694 AND nstd71 (11)
dbVar
SP53972 AND nstd71 (17)
dbVar
SP58077 AND nstd71 (9)
dbVar
PREDICTED: Homo sapiens copine 3 (CPNE3), transcript variant X3, mRNA
PREDICTED: Homo sapiens copine 3 (CPNE3), transcript variant X3, mRNA
gi|2462621509|ref|XM_054361450.1|

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