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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5845550copy number variation1nstd209human GRCh38 chr6: 5,452,975-5,453,974 , GRCh37.p13 chr6: 5,453,208-5,454,207 FARS2-AS1, FARS2
    nsv5673772copy number variation1nstd102humanPathogenic GRCh37 chr6: 5,368,784-5,545,593 , GRCh38.p12 chr6: 5,368,551-5,545,360 FARS2, FARS2-AS1
    nsv5471216copy number variation1nstd206human GRCh38 chr6: 5,335,835-5,459,461 , GRCh37.p13 chr6: 5,336,068-5,459,694 FARS2-AS1, FARS2
    nsv5462691copy number variation1nstd206human GRCh38 chr6: 5,429,363-5,460,766 , GRCh37.p13 chr6: 5,429,596-5,460,999 FARS2-AS1, FARS2
    nsv5207187mobile element deletion1nstd204human GRCh37.p13 chr6: 5,456,674-5,456,986 , GRCh38.p13 chr6: 5,456,441-5,456,753 FARS2, FARS2-AS1
    nsv4947529copy number variation1nstd200human GRCh38 chr6: 5,430,322-5,476,213 , GRCh37.p13 chr6: 5,430,555-5,476,446 FARS2, FARS2-AS1
    nsv4887503mobile element deletion1nstd200human GRCh38 chr6: 5,456,450-5,456,745 , GRCh37.p13 chr6: 5,456,683-5,456,978 FARS2-AS1, FARS2
    nsv4778503mobile element deletion1nstd200human GRCh37 chr6: 5,456,683-5,456,978 , GRCh38.p12 chr6: 5,456,450-5,456,745 FARS2, FARS2-AS1
    nsv4729467copy number variation1nstd102humanUncertain significance GRCh37 chr6: 5,105,467-5,623,386 , GRCh38.p12 chr6: 5,105,233-5,623,153 HNRNPA1P37, LYRM4-AS1, 4 more genes
    nsv4729312copy number variation1nstd102humanUncertain significance GRCh37 chr6: 5,317,360-5,604,139 , GRCh38.p12 chr6: 5,317,127-5,603,906 FARS2-AS1, FARS2
    nsv4675887copy number variation1nstd102humanUncertain significance GRCh37 chr6: 5,043,132-5,896,220 , GRCh38.p12 chr6: 5,042,898-5,895,987 TFB2MP1, LOC105374898, 9 more genes
    nsv4675617copy number variation1nstd102humanUncertain significance GRCh37 chr6: 5,176,631-5,854,127 , GRCh38.p12 chr6: 5,176,397-5,853,894 FARS2, LYRM4-AS1, 5 more genes
    nsv4675428copy number variation1nstd102humanUncertain significance GRCh37 chr6: 5,210,792-5,639,420 , GRCh38.p12 chr6: 5,210,558-5,639,187 HNRNPA1P37, LYRM4-AS1, 3 more genes
    nsv4675175copy number variation1nstd102humanUncertain significance GRCh37 chr6: 5,379,254-5,675,709 , GRCh38.p12 chr6: 5,379,021-5,675,476 FARS2, FARS2-AS1, 2 more genes
    nsv4675073copy number variation1nstd102humanUncertain significance GRCh37 chr6: 5,402,872-5,473,113 , GRCh38.p12 chr6: 5,402,639-5,472,880 FARS2, FARS2-AS1
    nsv4598644copy number variation1nstd183human GRCh37 chr6: 5,409,721-5,551,137 , GRCh38.p12 chr6: 5,409,488-5,550,904 FARS2, FARS2-AS1
    nsv4592840copy number variation1nstd183human GRCh37 chr6: 5,196,903-5,452,125 , GRCh38.p12 chr6: 5,196,669-5,451,892 LYRM4, LYRM4-AS1, 2 more genes
    nsv4456823copy number variation1nstd102humanUncertain significance GRCh37 chr6: 5,366,603-5,617,077 , GRCh38.p12 chr6: 5,366,370-5,616,844 HNRNPA1P37, FARS2, 1 more genes
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4456114copy number variation1nstd102humanUncertain significance GRCh37 chr6: 5,233,209-5,474,230 , GRCh38.p12 chr6: 5,232,976-5,473,997 FARS2, LYRM4-AS1, 2 more genes
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