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Items: 1 to 20 of 121

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5879519copy number variation1nstd209human GRCh38 chr1: 11,609,301-11,609,350 , GRCh37.p13 chr1: 11,669,358-11,669,407 LINC01647
    nsv5578488copy number variation1nstd207human GRCh38 chr1: 11,609,196-11,609,364 , GRCh37.p13 chr1: 11,669,253-11,669,421 LINC01647
    nsv5557473sequence alteration1nstd206human GRCh38 chr1: 10,919,048-11,710,696 , GRCh37.p13 chr1: 10,979,105-11,770,753 , ANGPTL7, 26 more genes
    nsv5428963copy number variation1nstd206human GRCh38 chr1: 11,609,242-11,609,341 , GRCh37.p13 chr1: 11,669,299-11,669,398 LINC01647
    nsv5299739copy number variation1nstd204human GRCh38.p13 chr1: 11,586,967-11,633,374 , GRCh37.p13 chr1: 11,647,024-11,693,431 LINC01647
    nsv5218807copy number variation1nstd204human GRCh38.p13 chr1: 11,586,928-11,630,712 , GRCh37.p13 chr1: 11,646,985-11,690,769 LINC01647
    nsv4889899copy number variation1nstd200human GRCh38 chr1: 11,586,975-11,633,365 , GRCh37.p13 chr1: 11,647,032-11,693,422 LINC01647
    nsv4782980copy number variation1nstd200human GRCh37 chr1: 11,647,032-11,693,422 , GRCh38.p12 chr1: 11,586,975-11,633,365 LINC01647
    nsv4728225copy number variation1nstd102humanUncertain significance GRCh37 chr1: 11,376,212-11,680,685 , GRCh38.p12 chr1: 11,316,155-11,620,628 DISP3, LINC01647, 4 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
    nsv4674634copy number variation1nstd102humanUncertain significance GRCh37 chr1: 11,419,867-11,676,100 , GRCh38.p12 chr1: 11,359,810-11,616,043 DISP3, LOC105376740, 3 more genes
    nsv4674003copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 9,852,396-11,909,475 , GRCh38.p12 chr1: 9,792,338-11,849,418 CLCN6, CORT, 59 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
    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
    nsv4436105copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-11,784,118 , GRCh38.p12 chr1: 82,154-11,724,061 PARK7, RNF223, 325 more genes
    nsv4377713copy number variation1nstd173human GRCh37 chr1: 11,632,115-11,673,777 , GRCh38.p12 chr1: 11,572,058-11,613,720 LINC01647
    nsv4036721copy number variation1nstd166human GRCh37.p13 chr1: 11,669,299-11,669,428 , GRCh38.p12 chr1: 11,609,242-11,609,371 LINC01647
    nsv3913790copy number variation1nstd102humanPathogenic NCBI36 chr1: 10,370,726-15,979,918 , GRCh37.p13 chr1: 10,448,139-16,107,331 , GRCh38.p12 chr1: 10,388,082-15,780,836 PRAMEF15, LOC105376759, 149 more genes
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