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Items: 1 to 20 of 35

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3890897copy number variation1nstd102humanBenign GRCh37 chr12: 31,743,234-31,744,033 , GRCh38.p12 chr12: 31,590,300-31,591,099 DENND5B, DENND5B-AS1
    nsv3898417copy number variation1nstd102humanBenign GRCh37 chr12: 31,743,194-31,743,834 , GRCh38.p12 chr12: 31,590,260-31,590,900 DENND5B, DENND5B-AS1
    nsv3895853copy number variation1nstd102humanBenign GRCh37 chr12: 31,743,194-31,743,690 , GRCh38.p12 chr12: 31,590,260-31,590,756 DENND5B, DENND5B-AS1
    nsv3898312copy number variation1nstd102humanBenign GRCh37 chr12: 31,743,319-31,743,690 , GRCh38.p12 chr12: 31,590,385-31,590,756 DENND5B, DENND5B-AS1
    nsv3891116copy number variation1nstd102humanBenign GRCh37 chr12: 31,641,592-31,766,895 , GRCh38.p12 chr12: 31,488,658-31,613,961 DENND5B, RPL31P50, 3 more genes
    nsv3893645copy number variation1nstd102humanBenign GRCh37 chr12: 31,743,194-31,750,910 , GRCh38.p12 chr12: 31,590,260-31,597,976 DENND5B, RPL31P50, 2 more genes
    nsv3893422copy number variation1nstd102humanBenign GRCh37 chr12: 31,743,194-31,748,491 , GRCh38.p12 chr12: 31,590,260-31,595,557 DENND5B, RPL31P50, 2 more genes
    nsv3912952copy number variation1nstd102humanPathogenic NCBI36 chr12: 25,308,034-34,108,730 , GRCh38 chr12: 25,263,833-34,064,528 , GRCh37 chr12: 25,416,767-34,217,463 DENND5B, LOC101060058, 125 more genes
    nsv3904242copy number variation1nstd102humanPathogenic GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309 DENND5B, RNA5SP369, 2454 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 DENND5B, LOH12CR2, 2452 more genes
    nsv3897722copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059 DENND5B, RNU4ATAC16P, 2452 more genes
    nsv3914194copy number variation1nstd102humanPathogenic NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807 DENND5B, BTG1P1, 2451 more genes
    nsv3904719copy number variation1nstd102humanPathogenic GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532 DENND5B, OR5BT1P, 2441 more genes
    nsv3914427copy number variation1nstd102humanPathogenic NCBI36 chr12: 18,636-36,150,744 , GRCh37.p13 chr12: 148,375-37,864,477 , GRCh38.p12 chr12: 43,334-37,470,675 DENND5B, LOC105369667, 684 more genes
    nsv3905633copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-37,869,301 , GRCh38.p12 chr12: 64,620-37,475,499 DENND5B, RESF1, 684 more genes
    nsv3897151copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-37,869,107 , GRCh38.p12 chr12: 64,620-37,475,305 DENND5B, CACNA2D4, 684 more genes
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 DENND5B, LOC105376675, 682 more genes
    nsv3924262copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,835,837 , GRCh38 chr12: 64,620-34,682,902 , NCBI36 chr12: 44,047-34,727,104 DENND5B, ENO2, 684 more genes
    nsv3901714copy number variation3nstd102humanPathogenic GRCh37 chr12: 173,786-34,835,837 , GRCh38.p12 chr12: 64,620-34,682,902 DENND5B, LOC105369677, 684 more genes
    nsv3911928copy number variation1nstd102humanPathogenic GRCh37 chr12: 282,465-34,761,006 , GRCh38 chr12: 54,427-34,608,071 , NCBI36 chr12: 33,854-34,652,273 DENND5B, IFT57P1, 684 more genes
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