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Items: 1 to 20 of 121

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5697349mobile element insertion2nstd211human GRCh38 chr11: 45,893,266-45,893,266 , GRCh37.p13 chr11: 45,914,817-45,914,817 MAPK8IP1
    nsv5659544insertion1nstd207human GRCh38 chr11: 45,893,251-45,893,251 , GRCh37.p13 chr11: 45,914,802-45,914,802 MAPK8IP1
    nsv5548576insertion1nstd206human GRCh38 chr11: 45,893,251-45,893,251 , GRCh37.p13 chr11: 45,914,802-45,914,802 MAPK8IP1
    nsv5513893copy number variation1nstd206human GRCh38 chr11: 45,900,944-45,901,100 , GRCh37.p13 chr11: 45,922,495-45,922,651 MAPK8IP1
    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
    nsv5380725copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 45,827,353-47,804,770 , GRCh38.p12 chr11: 45,805,802-47,783,218 MIR4688, LOC112268075, 58 more genes
    nsv5132027mobile element insertion1nstd203human GRCh38 chr11: 45,893,251-45,893,266 , GRCh37.p13 chr11: 45,914,802-45,914,817 MAPK8IP1
    nsv5123317mobile element insertion1nstd203human GRCh38 chr11: 45,889,178-45,889,195 , GRCh37.p13 chr11: 45,910,729-45,910,746 MAPK8IP1
    nsv4970943copy number variation1nstd200human GRCh38 chr11: 45,900,944-45,901,100 , GRCh37.p13 chr11: 45,922,495-45,922,651 MAPK8IP1
    nsv4970942copy number variation1nstd200human GRCh38 chr11: 45,890,893-45,893,023 , GRCh37.p13 chr11: 45,912,444-45,914,574 MAPK8IP1
    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
    nsv4729649copy number variation1nstd102humanUncertain significance GRCh37 chr11: 44,266,593-46,123,796 , GRCh38.p12 chr11: 44,245,043-46,102,245 LOC105376654, PHF21A, 31 more genes
    nsv4724813insertion2nstd186human GRCh37 chr11: 45,914,802-45,914,802 , GRCh38.p12 chr11: 45,893,251-45,893,251 MAPK8IP1
    nsv4714830copy number variation1nstd195human GRCh37 chr11: 45,760,601-46,177,151 , GRCh38.p12 chr11: 45,739,050-46,155,600 SLC35C1, LINC02716, 9 more genes
    nsv4689396mobile element insertion1nstd186human GRCh37 chr11: 45,914,817-45,914,817 , GRCh38.p12 chr11: 45,893,266-45,893,266 MAPK8IP1
    nsv4682898copy number variation1nstd102humanUncertain significance GRCh37 chr11: 45,827,333-45,932,533 , GRCh38.p12 chr11: 45,805,782-45,910,982 MAPK8IP1, CRY2, 3 more genes
    nsv4615986copy number variation1nstd183human GRCh37 chr11: 45,921,788-45,922,009 , GRCh38.p12 chr11: 45,900,237-45,900,458 MAPK8IP1
    nsv4542523insertion1nstd166human GRCh37.p13 chr11: 45,914,802-45,914,802 , GRCh38.p12 chr11: 45,893,251-45,893,251 MAPK8IP1
    nsv4492487mobile element insertion1nstd166human GRCh37.p13 chr11: 45,918,251-45,918,251 , GRCh38.p12 chr11: 45,896,700-45,896,700 MAPK8IP1
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