MS19008 AND nstd71 - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv898507	copy number variation	13	nstd71	human		NCBI36 chr11: 133,859,037-133,971,866 , GRCh37.p13 chr11: 134,353,827-134,466,656 , GRCh38.p12 chr11: 134,483,933-134,596,762	B3GAT1-DT
nsv906697	copy number variation	4	nstd71	human		NCBI36 chr16: 54,390,068-54,427,229 , GRCh37.p13 chr16: 55,832,567-55,869,728 , GRCh38.p12 chr16: 55,798,655-55,835,816	CES1
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
nsv908445	copy number variation	85	nstd71	human		NCBI36 chr17: 41,788,595-41,922,658 , GRCh37.p13 chr17: 44,432,855-44,566,775 , GRCh38.p12 chr17: 46,355,489-46,489,976	NSFP1, ARL17B
nsv904015	copy number variation	67	nstd71	human		NCBI36 chr15: 32,487,589-32,563,312 , GRCh37.p13 chr15: 34,700,297-34,776,020 , GRCh38.p12 chr15: 34,408,096-34,483,819	GOLGA8A, LOC100422491
nsv872992	copy number variation	87	nstd71	human		NCBI36 chr1: 194,977,690-195,089,653 , GRCh37.p13 chr1: 196,711,067-196,823,030 , GRCh38.p12 chr1: 196,741,937-196,853,900	LOC100996886, CFHR3, 2 more genes
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
nsv911912	copy number variation	43	nstd71	human		NCBI36 chr19: 48,060,801-48,160,500 , GRCh37.p13 chr19: 43,368,961-43,468,660 , GRCh38.p12 chr19: 42,864,809-42,964,508	CEACAMP7, PSG1, 2 more genes
nsv893199	copy number variation	58	nstd71	human		NCBI36 chr9: 43,532,092-43,641,682 , GRCh37.p13 chr9: 43,592,096-43,701,686 , GRCh38.p12 chr9: 42,112,703-42,222,293	CNTNAP3B, FAM74A7, 2 more genes
nsv906024	copy number variation	73	nstd71	human		NCBI36 chr16: 32,413,490-32,511,911 , GRCh37.p13 chr16: 32,505,989-32,604,410 , GRCh38.p12 chr16: 32,494,668-32,593,089	0
nsv889041	copy number variation	2	nstd71	human		NCBI36 chr7: 110,993,130-111,085,227 , GRCh37.p13 chr7: 111,205,894-111,297,991 , GRCh38.p12 chr7: 111,565,838-111,657,935	0
nsv903069	copy number variation	24	nstd71	human		NCBI36 chr15: 19,341,464-19,448,462 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr15\|NT_187602.1: 203,114-310,060 , GRCh38.p12 chr15\|NT_187382.1: 172,363-279,309	VN1R60P, NF1P9, 10 more genes
nsv872323	copy number variation	15	nstd71	human		NCBI36 chr1: 147,292,384-147,779,233 , GRCh37.p13 chr1: 149,025,760-149,512,609 , GRCh38.p12 chr16: 34,651,821-36,222,380	FRG2JP, RARRES2P9, 70 more genes
nsv890095	copy number variation	1	nstd71	human		NCBI36 chr8: 7,176,768-7,683,445 , GRCh37.p13 chr8: 7,189,358-7,646,035 , GRCh38.p12 chr8: 7,331,836-7,788,513	FAM90A19, FAM90A10, 36 more genes

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