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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5428480copy number variation1nstd206human GRCh38 chr1: 11,908,038-11,908,269 , GRCh37.p13 chr1: 11,968,095-11,968,326 RNU5E-4P, RNU5E-1
    nsv5422818copy number variation1nstd206human GRCh38 chr1: 11,909,250-11,917,654 , GRCh37.p13 chr1: 11,969,307-11,977,711 KIAA2013, RNU5E-4P
    nsv5295281copy number variation1nstd204human GRCh38.p13 chr1: 11,808,402-12,053,478 , GRCh37.p13 chr1: 11,868,459-12,113,535 RNU5E-1, RN7SL649P, 11 more genes
    nsv5210869copy number variation1nstd204human GRCh38.p13 chr1: 11,808,401-12,053,900 , GRCh37.p13 chr1: 11,868,458-12,113,957 NPPB, KIAA2013, 11 more genes
    nsv4903073copy number variation1nstd200human GRCh38 chr1: 11,910,411-11,921,841 , GRCh37.p13 chr1: 11,970,468-11,981,898 KIAA2013, RNU5E-4P
    nsv4903072copy number variation1nstd200human GRCh38 chr1: 11,909,116-11,945,255 , GRCh37.p13 chr1: 11,969,173-12,005,312 RNU5E-4P, PLOD1, 1 more genes
    nsv4903069copy number variation1nstd200human GRCh38 chr1: 11,808,412-12,053,469 , GRCh37.p13 chr1: 11,868,469-12,113,526 NPPB, MIIP, 11 more genes
    nsv4772168copy number variation1nstd200human GRCh37 chr1: 11,970,419-11,981,939 , GRCh38.p12 chr1: 11,910,362-11,921,882 RNU5E-4P, KIAA2013
    nsv4772167copy number variation1nstd200human GRCh37 chr1: 11,969,173-12,005,312 , GRCh38.p12 chr1: 11,909,116-11,945,255 PLOD1, KIAA2013, 1 more genes
    nsv4772165copy number variation1nstd200human GRCh37 chr1: 11,868,469-12,113,526 , GRCh38.p12 chr1: 11,808,412-12,053,469 RN7SL649P, RNU5E-1, 11 more genes
    nsv4681090copy number variation1nstd102humanUncertain significance GRCh37 chr1: 11,072,691-11,994,922 , GRCh38.p12 chr1: 11,012,634-11,934,865 FBXO44, LINC01647, 36 more genes
    nsv4579039copy number variation1nstd183human GRCh37 chr1: 11,923,982-11,971,749 , GRCh38.p12 chr1: 11,863,925-11,911,692 RNU5E-1, SBF1P2, 1 more genes
    nsv4454705copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,246,640-12,841,900 , GRCh38.p12 chr1: 10,186,582-12,781,757 LINC01647, MIR7846, 73 more genes
    nsv4453932copy number variation1nstd102humanUncertain significance GRCh37 chr1: 11,846,836-12,055,790 , GRCh38.p12 chr1: 11,786,779-11,995,733 MTHFR, C1orf167, 10 more genes
    nsv4436711copy number variation1nstd102humanPathogenic GRCh37 chr1: 11,794,553-12,786,444 , GRCh38.p12 chr1: 11,734,496-12,726,477 MIR4632, AADACL3, 31 more genes
    nsv4436680complex substitution1nstd102humanUncertain significance GRCh38.p12 chr1: 973,858-24,379,779 , GRCh37 chr1: 909,238-24,706,269 ALPL, RERE, 636 more genes
    nsv4436526complex substitution1nstd102humanUncertain significance GRCh38.p12 chr1: 973,858-16,409,637 , GRCh37 chr1: 909,238-16,736,132 RERE, CA6, 415 more genes
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 LINC01776, IGSF21-AS1, 1853 more genes
    nsv4346738copy number variation1nstd102humanPathogenic GRCh37 chr1: 11,690,766-12,835,739 , GRCh38.p12 chr1: 11,630,709-12,775,596 MIR6729, PLOD1, 38 more genes
    nsv4047778copy number variation1nstd166human GRCh37.p13 chr1: 11,968,406-11,968,476 , GRCh38.p12 chr1: 11,908,349-11,908,419 RNU5E-4P, RNU5E-1
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