1-0789-003 AND nstd173 - 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
nsv4379349	copy number variation	357	nstd173	human		GRCh37 chr20: 1,560,549-1,597,997 , GRCh38.p12 chr20: 1,579,903-1,617,351	SIRPB1
nsv4378261	copy number variation	1	nstd173	human		GRCh37 chr6: 159,929,460-159,986,505 , GRCh38.p12 chr6: 159,508,428-159,565,473	RPL21P69
nsv4375212	copy number variation	547	nstd173	human		GRCh37 chr1: 72,762,663-72,811,904 , GRCh38.p12 chr1: 72,296,980-72,346,221 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-67,446	RPL31P12, LOC105378797
nsv4366472	copy number variation	183	nstd173	human		GRCh37 chr3: 46,793,072-46,849,588 , GRCh38.p12 chr3: 46,751,582-46,808,098	PRSS44P, PRSS43P
nsv4365430	copy number variation	1	nstd173	human		GRCh37 chrX: 1,460,238-1,506,460 , GRCh38.p12 chrX: 1,341,345-1,387,567	IL3RA, , 2 more genes
nsv4367271	copy number variation	561	nstd173	human		GRCh37 chr11: 5,786,020-5,809,230 , GRCh38.p12 chr11: 5,764,790-5,788,000	OR56B2P, OR52N1, 1 more genes
nsv4376755	copy number variation	329	nstd173	human		GRCh37 chr14: 74,001,122-74,024,031 , GRCh38.p12 chr14: 73,534,418-73,557,327	ACOT1, NT5CP2, 1 more genes
nsv4385137	copy number variation	28	nstd173	human		GRCh37 chr5: 180,374,484-180,430,789 , GRCh38.p12 chr5: 180,947,484-181,003,789	TMEM69P2, LOC100128762, 3 more genes
nsv4369984	copy number variation	1	nstd173	human		GRCh37 chr6: 254,254-294,462 , GRCh38.p12 chr6: 254,254-294,462	, DUSP22, 1 more genes
nsv4376452	copy number variation	337	nstd173	human		GRCh37 chr17: 34,437,494-34,477,480 , GRCh38.p12 chr17: 36,110,101-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 64,198-104,195 , GRCh38.p12 chr17\|NT_187614.1: 345,022-385,008	LOC101927369, LOC107985055, 3 more genes
nsv4372953	copy number variation	1	nstd173	human		GRCh37 chr12: 8,558,475-8,595,531 , GRCh38.p12 chr12: 8,405,879-8,442,935	OR7E148P, OR7E140P, 1 more genes
nsv4382785	copy number variation	75	nstd173	human		GRCh37 chr12: 11,216,817-11,251,668 , GRCh38.p12 chr12: 11,064,218-11,099,069	TAS2R43, PRH1-TAS2R14, 3 more genes
nsv4371487	copy number variation	89	nstd173	human		GRCh37 chr19: 20,596,106-20,720,705 , GRCh38.p12 chr19: 20,413,300-20,537,899	ZNF826P, ZNF737, 4 more genes
nsv4371422	copy number variation	21	nstd173	human		GRCh37 chr3: 162,521,309-162,651,027 , GRCh38.p12 chr3: 162,803,521-162,933,239	0
nsv4381754	copy number variation	35	nstd173	human		GRCh37 chr16: 19,945,795-19,970,805 , GRCh38.p12 chr16: 19,934,473-19,959,483	0
nsv4369275	copy number variation	5	nstd173	human		GRCh37 chr19: 55,252,034-55,324,041 , GRCh38.p12 chr19\|NT_187693.1: 723,148-795,155	KIR2DL4, KIR2DL3, 4 more genes
nsv4372741	copy number variation	14	nstd173	human		GRCh37 chr6: 29,837,158-29,874,795 , GRCh38.p12 chr6: 29,869,381-29,907,018	HCG4P7, HLA-T, 4 more genes
nsv4372589	copy number variation	741	nstd173	human		GRCh37 chr14: 106,530,472-106,560,975 , GRCh38.p12 chr: NaN-NaN	0

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