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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7042992inversion1nstd229human GRCh38 chr3: 145,930,119-146,730,530 , GRCh37.p13 chr3: 145,647,906-146,448,317 PLSCR2, LNCSRLR, 8 more genes
    nsv6736165copy number variation1nstd229human GRCh38 chr3: 146,524,401-146,530,300 , GRCh37.p13 chr3: 146,242,188-146,248,087 PLSCR1
    nsv6735677copy number variation1nstd229human GRCh38 chr3: 146,474,664-146,609,522 , GRCh37.p13 chr3: 146,192,451-146,327,309 PLSCR5, RNU6-428P, 2 more genes
    nsv6729458copy number variation1nstd229human GRCh38 chr3: 146,527,211-146,527,556 , GRCh37.p13 chr3: 146,244,998-146,245,343 PLSCR1
    nsv6726185copy number variation1nstd229human GRCh38 chr3: 146,485,150-146,513,435 , GRCh37.p13 chr3: 146,202,937-146,231,222 PLSCR2, PLSCR1
    nsv6722757copy number variation1nstd229human GRCh38 chr3: 146,476,612-146,605,954 , GRCh37.p13 chr3: 146,194,399-146,323,741 PLSCR2, RNU6-428P, 2 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6562831inversion1nstd223human GRCh38 chr3: 142,555,219-148,451,915 , GRCh37.p13 chr3: 142,274,061-148,169,702 LOC102724145, PLS1, 60 more genes
    nsv6370486copy number variation1nstd223human GRCh38 chr3: 146,485,114-146,513,480 , GRCh37.p13 chr3: 146,202,901-146,231,267 PLSCR2, PLSCR1
    nsv6313678copy number variation1nstd102humanPathogenic GRCh37 chr3: 145,486,960-160,504,834 , GRCh38.p12 chr3: 145,769,173-160,787,046 RNU6-901P, RPL32P8, 229 more genes
    nsv6294406mobile element insertion1nstd186human GRCh37 chr3: 146,258,284-146,258,335 , GRCh38.p12 chr3: 146,540,497-146,540,548 PLSCR1
    nsv6290273copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,729,607-157,921,084 , GRCh38.p12 chr3: 143,010,765-158,203,295 LINC02066, TM4SF1-AS1, 206 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 LOC102724145, C3orf80, 273 more genes
    nsv6134994copy number variation1nstd213human GRCh37 chr3: 139,490,000-150,360,001 , GRCh38.p12 chr3: 139,771,158-150,642,214 , ATP1B3, 147 more genes
    nsv5991653copy number variation1nstd212human GRCh38 chr3: 146,528,153-146,528,298 , GRCh37.p13 chr3: 146,245,940-146,246,085 PLSCR1
    nsv5904622copy number variation1nstd209human GRCh38 chr3: 146,515,504-146,520,756 , GRCh37.p13 chr3: 146,233,291-146,238,543 PLSCR1
    nsv5834702copy number variation1nstd209human GRCh38 chr3: 146,515,614-146,520,767 , GRCh37.p13 chr3: 146,233,401-146,238,554 PLSCR1
    nsv5692001mobile element insertion1nstd211human GRCh38 chr3: 146,540,497-146,540,497 , GRCh37.p13 chr3: 146,258,284-146,258,284 PLSCR1
    nsv5680658mobile element insertion1nstd211human GRCh38 chr3: 146,545,009-146,545,009 , GRCh37.p13 chr3: 146,262,796-146,262,796 PLSCR1
    nsv5411773mobile element insertion1nstd206human GRCh38 chr3: 146,545,009-146,545,060 , GRCh37.p13 chr3: 146,262,796-146,262,847 PLSCR1
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