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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962783insertion1nstd209human GRCh38 chr1: 55,111,296-55,111,296 , GRCh37.p13 chr1: 55,576,969-55,576,969 USP24
    nsv5726851mobile element insertion1nstd211human GRCh38 chr1: 55,198,152-55,198,152 , GRCh37.p13 chr1: 55,663,825-55,663,825 USP24
    nsv5724160mobile element insertion1nstd211human GRCh38 chr1: 55,204,741-55,204,741 , GRCh37.p13 chr1: 55,670,414-55,670,414 USP24
    nsv5715419mobile element insertion1nstd211human GRCh38 chr1: 55,161,714-55,161,714 , GRCh37.p13 chr1: 55,627,387-55,627,387 USP24
    nsv5673255copy number variation1nstd102humanLikely pathogenic GRCh38.p12 chr1: 54,999,177-55,064,863 , GRCh37 chr1: 55,464,850-55,530,536 BSND, USP24, 1 more genes
    nsv5560129mobile element insertion1nstd206human GRCh38 chr1: 55,204,741-55,204,792 , GRCh37.p13 chr1: 55,670,414-55,670,465 USP24
    nsv5554420mobile element insertion1nstd206human GRCh38 chr1: 55,161,714-55,161,765 , GRCh37.p13 chr1: 55,627,387-55,627,438 USP24
    nsv5431093copy number variation1nstd206human GRCh38 chr1: 55,114,485-55,114,605 , GRCh37.p13 chr1: 55,580,158-55,580,278 USP24
    nsv5381135copy number variation1nstd102humanPathogenic GRCh37 chr1: 51,941,877-56,688,514 , GRCh38.p12 chr1: 51,476,205-56,222,842 LRP8-DT, LRRC42, 122 more genes
    nsv5287939copy number variation1nstd204human GRCh38.p13 chr1: 55,203,461-55,208,308 , GRCh37.p13 chr1: 55,669,134-55,673,981 USP24
    nsv5219280copy number variation1nstd204human GRCh38.p13 chr1: 55,203,401-55,208,100 , GRCh37.p13 chr1: 55,669,074-55,673,773 USP24
    nsv5216342copy number variation1nstd204human GRCh38.p13 chr1: 55,203,286-55,208,144 , GRCh37.p13 chr1: 55,668,959-55,673,817 USP24
    nsv5178892mobile element insertion1nstd203human GRCh38 chr1: 55,171,513-55,171,526 , GRCh37.p13 chr1: 55,637,186-55,637,199 USP24
    nsv5067322mobile element insertion1nstd203human GRCh38 chr1: 55,188,964-55,188,995 , GRCh37.p13 chr1: 55,654,637-55,654,668 USP24
    nsv5067091mobile element insertion1nstd203human GRCh38 chr1: 55,203,984-55,203,995 , GRCh37.p13 chr1: 55,669,657-55,669,668 USP24
    nsv5062200mobile element insertion1nstd203human GRCh38 chr1: 55,099,220-55,099,235 , GRCh37.p13 chr1: 55,564,893-55,564,908 USP24
    nsv4890290copy number variation1nstd200human GRCh38 chr1: 55,203,470-55,208,300 , GRCh37.p13 chr1: 55,669,143-55,673,973 USP24
    nsv4888344inversion1nstd200human GRCh37 chr1: 51,769,169-94,478,994 , GRCh38.p12 chr1: 51,303,497-94,013,438 , ST13P20, 664 more genes
    nsv4783319copy number variation1nstd200human GRCh37 chr1: 55,669,143-55,673,973 , GRCh38.p12 chr1: 55,203,470-55,208,300 USP24
    nsv4768338copy number variation1nstd102humanPathogenic GRCh37 chr1: 53,675,707-66,644,963 , GRCh38.p12 chr1: 53,210,035-66,179,280 TALDO1P1, LAMTOR5P1, 201 more genes
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