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Items: 1 to 20 of 92

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5918762copy number variation1nstd209human GRCh38 chr11: 58,832,259-58,997,961 , GRCh37.p13 chr11: 58,599,732-58,765,434 GLYATL1, GLYATL2, 5 more genes
    nsv5908645copy number variation1nstd209human GRCh38 chr11: 58,846,467-59,011,722 , GRCh37.p13 chr11: 58,613,940-58,779,195 GLYATL1, GLYATL2, 5 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5326104inversion1nstd204human GRCh37.p13 chr11: 58,446,123-60,252,987 , GRCh38.p13 chr11: 58,678,650-60,485,514 OSBP, OR5BB1P, 78 more genes
    nsv5325627inversion1nstd204human GRCh37.p13 chr11: 58,669,453-61,321,541 , GRCh38.p13 chr11: 58,901,980-61,554,069 , CD5, 118 more genes
    nsv5122754mobile element insertion1nstd203human GRCh38 chr11: 58,982,690-58,982,697 , GRCh37.p13 chr11: 58,750,163-58,750,170 GLYATL1P1, LOC283194
    nsv4984976copy number variation1nstd200human GRCh38 chr11: 58,959,228-58,979,279 , GRCh37.p13 chr11: 58,726,701-58,746,752 LOC100422398, LOC283194, 1 more genes
    nsv4984973copy number variation1nstd200human GRCh38 chr11: 58,629,506-59,462,358 , GRCh37.p13 chr11: 58,396,979-59,229,831 GLYATL1P4, LOC283194, 29 more genes
    nsv4885672inversion1nstd200human GRCh37 chr11: 58,669,461-61,321,541 , GRCh38.p12 chr11: 58,901,988-61,554,069 , MS4A2, 118 more genes
    nsv4870911inversion1nstd200human GRCh37 chr11: 58,446,132-60,252,987 , GRCh38.p12 chr11: 58,678,659-60,485,514 LOC100422398, LOC100287485, 78 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4729406copy number variation1nstd102humanUncertain significance GRCh37 chr11: 58,602,498-59,091,934 , GRCh38.p12 chr11: 58,835,025-59,324,461 LOC100422398, LOC643709, 20 more genes
    nsv4685714copy number variation1nstd102humannot provided GRCh37 chr11: 58,237,819-58,800,374 , GRCh38.p12 chr11: 58,470,346-59,032,901 GLYATL1, LPXN, 14 more genes
    nsv4615718copy number variation1nstd183human GRCh37 chr11: 58,723,976-58,751,676 , GRCh38.p12 chr11: 58,956,503-58,984,203 GLYATL1, GLYATL1P1, 2 more genes
    nsv4207706copy number variation1nstd166human GRCh37.p13 chr11: 58,483,577-58,779,220 , GRCh38.p12 chr11: 58,716,104-59,011,747 LOC100422398, GLYATL1, 8 more genes
    nsv4203865copy number variation1nstd166human GRCh37.p13 chr11: 58,752,537-58,753,299 , GRCh38.p12 chr11: 58,985,064-58,985,826 GLYATL1P1, LOC283194
    nsv3918789copy number variation1nstd102humanUncertain significance NCBI36 chr11: 58,356,508-58,603,428 , GRCh37.p13 chr11: 58,599,932-58,846,852 , GRCh38.p12 chr11: 58,832,459-59,079,379 GLYATL1P1, GLYATL2, 6 more genes
    nsv3911150copy number variation1nstd102humanPathogenic GRCh37 chr11: 55,086,995-58,766,250 , NCBI36 chr11: 54,843,571-58,522,826 , GRCh38 chr11: 55,319,519-58,998,777 OR5BD1P, SELENOH, 197 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
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