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Items: 1 to 20 of 199

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054116inversion1nstd229human GRCh38 chr3: 19,170,573-20,582,118 , GRCh37.p13 chr3: 19,212,065-20,623,610 SGO1, EFHB, 17 more genes
    nsv7051519inversion1nstd229human GRCh38 chr3: 19,693,381-21,117,946 , GRCh37.p13 chr3: 19,734,873-21,159,438 LOC107986068, PP2D1, 16 more genes
    nsv7047955inversion1nstd229human GRCh38 chr3: 16,742,381-21,099,619 , GRCh37.p13 chr3: 16,783,888-21,141,111 PP2D1, TRC-GCA25-1, 37 more genes
    nsv7046868inversion1nstd229human GRCh38 chr3: 17,344,159-22,155,377 , GRCh37.p13 chr3: 17,385,651-22,196,869 LOC105376981, LOC107986066, 39 more genes
    nsv7046806inversion1nstd229human GRCh38 chr3: 20,346,245-20,346,524 , GRCh37.p13 chr3: 20,387,737-20,388,016 LOC101927829
    nsv6712880copy number variation1nstd229human GRCh38 chr3: 20,293,798-20,510,673 , GRCh37.p13 chr3: 20,335,290-20,552,165 RNU6-815P, LOC101927829
    nsv6711980copy number variation1nstd229human GRCh38 chr3: 20,280,325-20,394,664 , GRCh37.p13 chr3: 20,321,817-20,436,156 LOC101927829
    nsv6709227copy number variation1nstd229human GRCh38 chr3: 20,178,701-20,412,300 , GRCh37.p13 chr3: 20,220,193-20,453,792 SGO1-AS1, LOC101927829, 3 more genes
    nsv6703622copy number variation1nstd229human GRCh38 chr3: 19,444,707-20,918,143 , GRCh37.p13 chr3: 19,486,199-20,959,635 RNU6-815P, SAP18P3, 17 more genes
    nsv6634367copy number variation1nstd102humanPathogenic GRCh37 chr3: 13,836,340-25,357,427 , GRCh38.p12 chr3: 13,794,843-25,315,936 TMEM43, SLC6A6, 132 more genes
    nsv6628755copy number variation1nstd224human GRCh37 chr3: 20,374,929-20,388,173 , GRCh38.p12 chr3: 20,333,437-20,346,681 , GRCh38.p12 chr3|NT_187535.1: 60,022-73,266 LOC101927829
    nsv6628754copy number variation1nstd224human GRCh37 chr3: 20,256,334-20,384,627 , GRCh38.p12 chr3: 20,214,842-20,343,135 , GRCh38.p12 chr3|NT_187535.1: 1-69,720 RNU6-822P, LOC101927829
    nsv6545573inversion1nstd223human GRCh38 chr3: 16,746,915-21,192,302 , GRCh37.p13 chr3: 16,788,422-21,233,794 TBC1D5, SATB1, 38 more genes
    nsv6368977copy number variation1nstd223human GRCh38 chr3: 20,346,101-20,451,600 , GRCh37.p13 chr3: 20,387,593-20,493,092 LOC101927829
    nsv6359511copy number variation1nstd223human GRCh38 chr3: 20,280,401-20,341,600 , GRCh37.p13 chr3: 20,321,893-20,383,092 LOC101927829
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 LOC102724104, CRIP1P2, 291 more genes
    nsv6296920copy number variation1nstd186human GRCh37 chr3: 20,390,948-20,541,310 , GRCh38.p12 chr3: 20,349,456-20,499,818 LOC101927829
    nsv6294475mobile element insertion1nstd186human GRCh37 chr3: 20,385,030-20,385,081 , GRCh38.p12 chr3: 20,343,538-20,343,589 , GRCh38.p12 chr3|NT_187535.1: 70,123-70,174 LOC101927829
    nsv5993279copy number variation1nstd212human GRCh38 chr3: 20,346,234-20,346,295 , GRCh37.p13 chr3: 20,387,726-20,387,787 LOC101927829
    nsv5892001copy number variation1nstd209human GRCh38 chr3: 20,054,861-20,362,981 , GRCh37.p13 chr3: 20,096,353-20,404,473 , KAT2B, 6 more genes
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