U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 802

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv6130755insertion1nstd186human GRCh37 chr21: 20,118,444-20,118,494 , GRCh38.p12 chr21: 18,746,126-18,746,176 MIR548XHG
    nsv5973730insertion1nstd209human GRCh38 chr21: 18,697,026-18,697,026 , GRCh37.p13 chr21: 20,069,344-20,069,344 MIR548XHG
    nsv5972396insertion1nstd209human GRCh38 chr21: 18,674,579-18,674,579 , GRCh37.p13 chr21: 20,046,897-20,046,897 MIR548XHG
    nsv5965857copy number variation1nstd209human GRCh38 chr21: 14,377,888-22,678,896 , GRCh37.p13 chr21: 15,750,209-24,051,216 , LOC107985508, 80 more genes
    nsv5965625copy number variation1nstd209human GRCh38 chr21: 18,587,216-18,587,417 , GRCh37.p13 chr21: 19,959,534-19,959,735 MIR548XHG
    nsv5960016copy number variation1nstd209human GRCh38 chr21: 18,684,478-18,708,704 , GRCh37.p13 chr21: 20,056,796-20,081,022 MIR548XHG, MIR548X
    nsv5956348copy number variation1nstd209human GRCh38 chr21: 18,751,562-18,751,877 , GRCh37.p13 chr21: 20,123,880-20,124,195 MIR548XHG
    nsv5949009copy number variation1nstd209human GRCh38 chr21: 18,746,176-18,746,231 , GRCh37.p13 chr21: 20,118,494-20,118,549 MIR548XHG
    nsv5885519copy number variation2nstd209human GRCh38 chr21: 18,688,500-18,691,798 , GRCh37.p13 chr21: 20,060,818-20,064,116 MIR548XHG
    nsv5885187copy number variation2nstd209human GRCh38 chr21: 18,688,499-18,691,398 , GRCh37.p13 chr21: 20,060,817-20,063,716 MIR548XHG
    nsv5884148copy number variation1nstd209human GRCh38 chr21: 18,691,599-18,693,998 , GRCh37.p13 chr21: 20,063,917-20,066,316 MIR548XHG
    nsv5883777copy number variation1nstd209human GRCh38 chr21: 18,690,611-18,694,998 , GRCh37.p13 chr21: 20,062,929-20,067,316 MIR548XHG
    nsv5873415copy number variation1nstd209human GRCh38 chr21: 18,561,449-18,567,751 , GRCh37.p13 chr21: 19,933,767-19,940,069 MIR548XHG
    nsv5870467copy number variation1nstd209human GRCh38 chr21: 18,692,199-18,707,156 , GRCh37.p13 chr21: 20,064,517-20,079,474 MIR548XHG
    nsv5870400copy number variation2nstd209human GRCh38 chr21: 18,568,278-18,569,640 , GRCh37.p13 chr21: 19,940,596-19,941,958 MIR548XHG
    nsv5868409copy number variation2nstd209human GRCh38 chr21: 18,684,699-18,691,698 , GRCh37.p13 chr21: 20,057,017-20,064,016 MIR548X, MIR548XHG
    nsv5720956mobile element insertion1nstd211human GRCh38 chr21: 18,688,708-18,688,708 , GRCh37.p13 chr21: 20,061,026-20,061,026 MIR548XHG
    nsv5701382mobile element insertion2nstd211human GRCh38 chr21: 18,709,035-18,709,035 , GRCh37.p13 chr21: 20,081,353-20,081,353 MIR548XHG
    nsv5694522mobile element insertion1nstd211human GRCh38 chr21: 18,714,980-18,714,980 , GRCh37.p13 chr21: 20,087,298-20,087,298 MIR548XHG
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center