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 144

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5950938copy number variation1nstd209human GRCh38 chr20: 20,032,015-20,032,456 , GRCh37.p13 chr20: 20,012,659-20,013,100 NAA20, CRNKL1
    nsv5697980mobile element insertion2nstd211human GRCh38 chr20: 20,046,038-20,046,038 , GRCh37.p13 chr20: 20,026,682-20,026,682 CRNKL1
    nsv5695163mobile element insertion1nstd211human GRCh38 chr20: 20,048,098-20,048,098 , GRCh37.p13 chr20: 20,028,742-20,028,742 CRNKL1
    nsv5515004copy number variation1nstd206human GRCh38 chr20: 20,032,015-20,032,459 , GRCh37.p13 chr20: 20,012,659-20,013,103 CRNKL1, NAA20
    nsv5425396mobile element insertion1nstd206human GRCh38 chr20: 20,048,098-20,048,149 , GRCh37.p13 chr20: 20,028,742-20,028,793 CRNKL1
    nsv5423052mobile element insertion1nstd206human GRCh38 chr20: 20,046,038-20,046,089 , GRCh37.p13 chr20: 20,026,682-20,026,733 CRNKL1
    nsv5389730copy number variation3nstd186human GRCh37 chr20: 20,012,659-20,013,103 , GRCh38.p12 chr20: 20,032,015-20,032,459 NAA20, CRNKL1
    nsv5320460copy number variation1nstd204human GRCh37.p13 chr20: 20,012,654-20,013,112 , GRCh38.p13 chr20: 20,032,010-20,032,468 CRNKL1, NAA20
    nsv5177004mobile element insertion1nstd203human GRCh38 chr20: 20,046,023-20,046,038 , GRCh37.p13 chr20: 20,026,667-20,026,682 CRNKL1
    nsv5167519mobile element insertion1nstd203human GRCh38 chr20: 20,046,025-20,046,038 , GRCh37.p13 chr20: 20,026,669-20,026,682 CRNKL1
    nsv5021635copy number variation1nstd200human GRCh38 chr20: 20,032,015-20,032,459 , GRCh37.p13 chr20: 20,012,659-20,013,103 CRNKL1, NAA20
    nsv4862275copy number variation1nstd200human GRCh37 chr20: 20,012,659-20,013,103 , GRCh38.p12 chr20: 20,032,015-20,032,459 NAA20, CRNKL1
    nsv4729757copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 19,750,804-30,479,077 , GRCh38.p12 chr20: 19,770,160-31,891,274 BCL2L1, CD24P3, 222 more genes
    nsv4676419copy number variation1nstd102humanPathogenic GRCh37 chr20: 8,571,696-22,088,650 , GRCh38.p12 chr20: 8,591,049-22,108,012 PGAM3P, EEF1A1P34, 182 more genes
    nsv4669855copy number variation1nstd186human GRCh37 chr20: 20,012,659-20,013,103 , GRCh38.p12 chr20: 20,032,015-20,032,459 NAA20, CRNKL1
    nsv4643517copy number variation1nstd186human GRCh37 chr20: 20,012,659-20,013,113 , GRCh38.p12 chr20: 20,032,015-20,032,469 NAA20, CRNKL1
    nsv4630627copy number variation1nstd183human GRCh37 chr20: 20,012,659-20,013,103 , GRCh38.p12 chr20: 20,032,015-20,032,459 CRNKL1, NAA20
    nsv4507426mobile element insertion1nstd166human GRCh37.p13 chr20: 20,026,667-20,026,667 , GRCh38.p12 chr20: 20,046,023-20,046,023 CRNKL1
    nsv4430563copy number variation1nstd174human GRCh37 chr20: 20,012,556-20,013,103 , GRCh38.p12 chr20: 20,031,912-20,032,459 NAA20, CRNKL1
    nsv4349190copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38.p12 chr20: 80,927-26,324,843 LOC105372582, LOC101929937, 473 more genes
    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