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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5636930insertion2nstd207human GRCh38 chr9: 126,876,199-126,876,199 , GRCh37.p13 chr9: 129,638,478-129,638,478 ZBTB34
    nsv5630402insertion3nstd207human GRCh38 chr9: 126,876,197-126,876,197 , GRCh37.p13 chr9: 129,638,476-129,638,476 ZBTB34
    nsv5564479copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr9: 129,376,729-131,016,993 , GRCh38.p12 chr9: 126,614,450-128,254,714 PIP5KL1, MIR3911, 50 more genes
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4985722copy number variation1nstd200human GRCh38 chr9: 126,420,321-126,891,592 , GRCh37.p13 chr9: 129,182,600-129,653,871 MVB12B, LOC105376276, 5 more genes
    nsv4768372copy number variation1nstd102humanPathogenic GRCh37 chr9: 128,512,347-130,702,572 , GRCh38.p12 chr9: 125,750,068-127,940,293 LOC105379841, PTRH1, 47 more genes
    nsv4763356insertion1nstd199human GRCh37 chr9: 129,638,437-129,638,437 , GRCh38.p12 chr9: 126,876,158-126,876,158 ZBTB34
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4448096insertion1nstd175human GRCh37 chr9: 129,638,427-129,638,427 , GRCh38.p12 chr9: 126,876,148-126,876,148 ZBTB34
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4190349copy number variation1nstd166human GRCh37.p13 chr9: 129,635,907-129,641,631 , GRCh38.p12 chr9: 126,873,628-126,879,352 ZBTB34
    nsv4186064copy number variation1nstd166human GRCh37.p13 chr9: 129,618,000-129,660,000 , GRCh38.p12 chr9: 126,855,721-126,897,721 ZBTB34
    nsv4183199copy number variation1nstd166human GRCh37.p13 chr9: 129,633,000-129,642,000 , GRCh38.p12 chr9: 126,870,721-126,879,721 ZBTB34
    nsv3958217insertion1nstd168human GRCh38 chr9: 126,870,511-126,886,192 , GRCh37.p13 chr9: 129,632,790-129,648,471 ZBTB34
    nsv3951603insertion1nstd167human GRCh37 chr9: 129,638,476-129,638,476 , GRCh38.p12 chr9: 126,876,197-126,876,197 ZBTB34
    nsv3924370copy number variation1nstd102humanPathogenic NCBI36 chr9: 126,857,965-130,440,046 , GRCh38 chr9: 125,055,865-128,637,946 , GRCh37 chr9: 127,818,144-131,400,225 MVB12B, MIR4672, 97 more genes
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
    nsv3921944copy number variation1nstd102humanPathogenic GRCh38 chr9: 126,081,595-127,781,685 , NCBI36 chr9: 127,883,695-129,583,785 , GRCh37 chr9: 128,843,874-130,543,964 LOC101929116, LRSAM1, 30 more genes
    nsv3921598copy number variation1nstd102humanPathogenic GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389 PGAP4, ECPAS, 2167 more genes
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