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 484

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962878copy number variation1nstd209human GRCh38 chr21: 43,739,501-43,740,992 , GRCh37.p13 chr21: 45,159,382-45,160,873 PDXK
    nsv5962173copy number variation1nstd209human GRCh38 chr21: 43,731,656-43,731,705 , GRCh37.p13 chr21: 45,151,537-45,151,586 PDXK
    nsv5959369copy number variation1nstd209human GRCh38 chr21: 43,701,500-43,717,832 , GRCh37.p13 chr21: 45,121,381-45,137,713 PDXK
    nsv5877822copy number variation1nstd209human GRCh38 chr21: 43,739,493-43,740,792 , GRCh37.p13 chr21: 45,159,374-45,160,673 PDXK
    nsv5672510insertion1nstd207human GRCh38 chr21: 43,743,424-43,743,424 , GRCh37.p13 chr21: 45,163,305-45,163,305 PDXK
    nsv5672010insertion1nstd207human GRCh38 chr21: 43,741,151-43,741,151 , GRCh37.p13 chr21: 45,161,032-45,161,032 PDXK
    nsv5671977insertion1nstd207human GRCh38 chr21: 43,743,497-43,743,497 , GRCh37.p13 chr21: 45,163,378-45,163,378 PDXK
    nsv5671952insertion1nstd207human GRCh38 chr21: 43,741,395-43,741,395 , GRCh37.p13 chr21: 45,161,276-45,161,276 PDXK
    nsv5668188insertion1nstd207human GRCh38 chr21: 43,741,350-43,741,350 , GRCh37.p13 chr21: 45,161,231-45,161,231 PDXK
    nsv5666343insertion1nstd207human GRCh38 chr21: 43,741,200-43,741,200 , GRCh37.p13 chr21: 45,161,081-45,161,081 PDXK
    nsv5666098insertion1nstd207human GRCh38 chr21: 43,741,454-43,741,454 , GRCh37.p13 chr21: 45,161,335-45,161,335 PDXK
    nsv5665938insertion1nstd207human GRCh38 chr21: 43,741,447-43,741,447 , GRCh37.p13 chr21: 45,161,328-45,161,328 PDXK
    nsv5601240copy number variation1nstd207human GRCh38 chr21: 43,741,246-43,741,360 , GRCh37.p13 chr21: 45,161,127-45,161,241 PDXK
    nsv5599684copy number variation1nstd207human GRCh38 chr21: 43,739,501-43,740,992 , GRCh37.p13 chr21: 45,159,382-45,160,873 PDXK
    nsv5592248copy number variation1nstd207human GRCh38 chr21: 43,743,118-43,743,168 , GRCh37.p13 chr21: 45,162,999-45,163,049 PDXK
    nsv5585464copy number variation1nstd207human GRCh38 chr21: 43,741,327-43,741,382 , GRCh37.p13 chr21: 45,161,208-45,161,263 PDXK
    nsv5564322copy number variation2nstd102humanUncertain significance GRCh37 chr21: 44,838,130-45,196,150 , GRCh38.p12 chr21: 43,418,250-43,776,269 LINC00319, HSF2BP, 10 more genes
    nsv5546473insertion1nstd206human GRCh38 chr21: 43,742,497-43,742,533 , GRCh37.p13 chr21: 45,162,378-45,162,414 PDXK
    nsv5536405copy number variation1nstd206human GRCh38 chr21: 43,737,513-43,737,617 , GRCh37.p13 chr21: 45,157,394-45,157,498 PDXK, LOC105372824
    nsv5534664copy number variation1nstd206human GRCh38 chr21: 43,739,505-43,740,993 , GRCh37.p13 chr21: 45,159,386-45,160,874 PDXK
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

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