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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935857copy number variation1nstd209human GRCh38 chr19: 55,709,313-55,716,660 , GRCh37.p13 chr19: 56,220,679-56,228,026 NLRP9, EPN1
    nsv5928600copy number variation1nstd209human GRCh38 chr19: 55,714,278-55,714,384 , GRCh37.p13 chr19: 56,225,644-56,225,750 NLRP9
    nsv5870650copy number variation1nstd209human GRCh38 chr19: 55,734,644-55,737,481 , GRCh37.p13 chr19: 56,246,010-56,248,847 NLRP9, RN7SKP109
    nsv5867761copy number variation1nstd209human GRCh38 chr19: 55,709,275-55,716,663 , GRCh37.p13 chr19: 56,220,641-56,228,029 EPN1, NLRP9
    nsv5702199mobile element insertion2nstd211human GRCh38 chr19: 55,724,374-55,724,374 , GRCh37.p13 chr19: 56,235,740-56,235,740 NLRP9
    nsv5653297insertion2nstd207human GRCh38 chr19: 55,712,960-55,712,960 , GRCh37.p13 chr19: 56,224,326-56,224,326 NLRP9
    nsv5644759insertion2nstd207human GRCh38 chr19: 55,713,697-55,713,697 , GRCh37.p13 chr19: 56,225,063-56,225,063 NLRP9
    nsv5530162copy number variation1nstd206human GRCh38 chr19: 55,709,729-55,709,885 , GRCh37.p13 chr19: 56,221,095-56,221,251 NLRP9, EPN1
    nsv5526904copy number variation1nstd206human GRCh38 chr19: 55,729,836-55,792,106 , GRCh37.p13 chr19: 56,241,202-56,303,472 NLRP11, NLRP9, 5 more genes
    nsv5520334copy number variation1nstd206human GRCh38 chr19: 55,712,181-55,712,302 , GRCh37.p13 chr19: 56,223,547-56,223,668 NLRP9
    nsv5518708copy number variation1nstd206human GRCh38 chr19: 55,734,352-55,737,772 , GRCh37.p13 chr19: 56,245,718-56,249,138 RN7SKP109, NLRP9
    nsv5517546copy number variation1nstd206human GRCh38 chr19: 55,724,203-55,728,562 , GRCh37.p13 chr19: 56,235,569-56,239,928 NLRP9
    nsv5423077mobile element insertion1nstd206human GRCh38 chr19: 55,724,374-55,724,425 , GRCh37.p13 chr19: 56,235,740-56,235,791 NLRP9
    nsv5287923copy number variation1nstd204human GRCh38.p13 chr19: 55,728,489-55,730,055 , GRCh37.p13 chr19: 56,239,855-56,241,421 NLRP9
    nsv5160924mobile element insertion1nstd203human GRCh38 chr19: 55,724,360-55,724,371 , GRCh37.p13 chr19: 56,235,726-56,235,737 NLRP9
    nsv5028104copy number variation1nstd200human GRCh38 chr19: 55,734,504-55,739,784 , GRCh37.p13 chr19: 56,245,870-56,251,150 NLRP9, RN7SKP109
    nsv5028103copy number variation1nstd200human GRCh38 chr19: 55,733,941-55,741,859 , GRCh37.p13 chr19: 56,245,307-56,253,225 RN7SKP109, NLRP9
    nsv5028102copy number variation1nstd200human GRCh38 chr19: 55,724,203-55,728,562 , GRCh37.p13 chr19: 56,235,569-56,239,928 NLRP9
    nsv5028101copy number variation1nstd200human GRCh38 chr19: 55,716,507-55,719,334 , GRCh37.p13 chr19: 56,227,873-56,230,700 NLRP9
    nsv5024974copy number variation1nstd200human GRCh38 chr19: 55,734,124-55,870,344 , GRCh37.p13 chr19: 56,245,490-56,381,710 RN7SKP109, NLRP4, 6 more genes
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