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Items: 1 to 20 of 331

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963924insertion1nstd209human GRCh38 chr1: 220,576,004-220,576,004 , GRCh37.p13 chr1: 220,749,346-220,749,346 MARK1
    nsv5729515mobile element insertion1nstd211human GRCh38 chr1: 220,655,349-220,655,349 , GRCh37.p13 chr1: 220,828,691-220,828,691 MARK1
    nsv5724243mobile element insertion1nstd211human GRCh38 chr1: 220,527,255-220,527,255 , GRCh37.p13 chr1: 220,700,597-220,700,597 MARK1
    nsv5620658insertion1nstd207human GRCh38 chr1: 220,576,004-220,576,004 , GRCh37.p13 chr1: 220,749,346-220,749,346 MARK1
    nsv5560375mobile element insertion1nstd206human GRCh38 chr1: 220,527,255-220,527,306 , GRCh37.p13 chr1: 220,700,597-220,700,648 MARK1
    nsv5559037mobile element insertion1nstd206human GRCh38 chr1: 220,655,349-220,655,400 , GRCh37.p13 chr1: 220,828,691-220,828,742 MARK1
    nsv5542631insertion1nstd206human GRCh38 chr1: 220,576,017-220,576,055 , GRCh37.p13 chr1: 220,749,359-220,749,397 MARK1
    nsv5450175copy number variation1nstd206human GRCh38 chr1: 220,633,330-220,633,405 , GRCh37.p13 chr1: 220,806,672-220,806,747 MARK1
    nsv5445048copy number variation1nstd206human GRCh38 chr1: 220,664,459-220,664,545 , GRCh37.p13 chr1: 220,837,801-220,837,887 MARK1
    nsv5440527copy number variation1nstd206human GRCh38 chr1: 220,575,965-220,577,938 , GRCh37.p13 chr1: 220,749,307-220,751,280 MARK1
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5355472translocation1nstd200human GRCh38 chr11: 83,316,599-83,316,599 , GRCh38 chr1: 220,647,240-220,647,240 , GRCh37.p13 chr11: 83,027,642-83,027,642 , GRCh37.p13 chr1: 220,820,582-220,820,582 MARK1
    nsv5339289translocation1nstd200human GRCh37 chr1: 220,823,535-220,823,535 , GRCh37 chr1: 220,823,627-220,823,627 , GRCh38.p12 chr1: 220,650,193-220,650,193 , GRCh38.p12 chr1: 220,650,285-220,650,285 MARK1
    nsv5214923copy number variation1nstd204human GRCh38.p13 chr1: 220,533,901-220,536,400 , GRCh37.p13 chr1: 220,707,243-220,709,742 MARK1
    nsv5164435mobile element insertion1nstd203human GRCh38 chr1: 220,655,338-220,655,349 , GRCh37.p13 chr1: 220,828,680-220,828,691 MARK1
    nsv5069562mobile element insertion1nstd203human GRCh38 chr1: 220,604,751-220,604,763 , GRCh37.p13 chr1: 220,778,093-220,778,105 MARK1
    nsv5067811mobile element insertion1nstd203human GRCh38 chr1: 220,617,720-220,617,734 , GRCh37.p13 chr1: 220,791,062-220,791,076 MARK1
    nsv5066078mobile element insertion1nstd203human GRCh38 chr1: 220,543,786-220,543,798 , GRCh37.p13 chr1: 220,717,128-220,717,140 MARK1
    nsv5064013mobile element insertion1nstd203human GRCh38 chr1: 220,658,263-220,658,279 , GRCh37.p13 chr1: 220,831,605-220,831,621 MARK1
    nsv4898839copy number variation1nstd200human GRCh38 chr1: 220,650,193-220,650,285 , GRCh37.p13 chr1: 220,823,535-220,823,627 MARK1
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