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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906457copy number variation1nstd209human GRCh38 chr2: 198,342,576-198,342,631 , GRCh37.p13 chr2: 199,207,300-199,207,355 LINC01923
    nsv5687723mobile element insertion2nstd211human GRCh38 chr2: 198,315,351-198,315,351 , GRCh37.p13 chr2: 199,180,075-199,180,075 LINC01923
    nsv5621056insertion1nstd207human GRCh38 chr2: 198,342,576-198,342,576 , GRCh37.p13 chr2: 199,207,300-199,207,300 LINC01923
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5450615copy number variation1nstd206human GRCh38 chr2: 198,303,676-198,305,385 , GRCh37.p13 chr2: 199,168,400-199,170,109 LINC01923
    nsv5447705copy number variation1nstd206human GRCh38 chr2: 198,342,576-198,342,649 , GRCh37.p13 chr2: 199,207,300-199,207,373 LINC01923
    nsv5436855copy number variation1nstd206human GRCh38 chr2: 198,305,483-198,305,595 , GRCh37.p13 chr2: 199,170,207-199,170,319 LINC01923
    nsv5395523mobile element insertion1nstd206human GRCh38 chr2: 198,315,351-198,315,402 , GRCh37.p13 chr2: 199,180,075-199,180,126 LINC01923
    nsv5182762mobile element insertion1nstd203human GRCh38 chr2: 198,322,128-198,322,144 , GRCh37.p13 chr2: 199,186,852-199,186,868 LINC01923
    nsv5065201mobile element insertion1nstd203human GRCh38 chr2: 198,315,338-198,315,347 , GRCh37.p13 chr2: 199,180,062-199,180,071 LINC01923
    nsv4913804copy number variation1nstd200human GRCh38 chr2: 198,369,400-198,369,562 , GRCh37.p13 chr2: 199,234,124-199,234,286 LINC01923
    nsv4913803copy number variation1nstd200human GRCh38 chr2: 198,253,224-198,311,633 , GRCh37.p13 chr2: 199,117,948-199,176,357 LINC01923
    nsv4910233copy number variation1nstd200human GRCh38 chr2: 198,298,776-198,304,184 , GRCh37.p13 chr2: 199,163,500-199,168,908 LINC01923
    nsv4795465copy number variation1nstd200human GRCh37 chr2: 199,163,500-199,168,908 , GRCh38.p12 chr2: 198,298,776-198,304,184 LINC01923
    nsv4768322copy number variation1nstd102humanPathogenic GRCh37 chr2: 197,359,024-201,383,462 , GRCh38.p12 chr2: 196,494,300-200,518,739 ANKRD44-DT, ATP5MC2P3, 48 more genes
    nsv4750680insertion1nstd199human GRCh37 chr2: 199,207,351-199,207,351 , GRCh38.p12 chr2: 198,342,627-198,342,627 LINC01923
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4716529copy number variation1nstd102humanPathogenic GRCh37 chr2: 190,345,272-200,212,289 , GRCh38.p12 chr2: 189,480,546-199,347,566 C2orf66, LINC01821, 105 more genes
    nsv4674383copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,233,162-211,927,188 , GRCh38.p12 chr2: 162,376,652-211,062,464 SNORA41, LOC101929633, 663 more genes
    nsv4659411copy number variation1nstd186human GRCh37 chr2: 199,168,397-199,170,103 , GRCh38.p12 chr2: 198,303,673-198,305,379 LINC01923
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