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Items: 1 to 20 of 272

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5952151insertion1nstd209human GRCh38 chr4: 122,875,427-122,875,427 , GRCh37.p13 chr4: 123,796,582-123,796,582 FGF2
    nsv5905599copy number variation1nstd209human GRCh38 chr4: 122,863,948-122,864,002 , GRCh37.p13 chr4: 123,785,103-123,785,157 FGF2
    nsv5686875mobile element insertion2nstd211human GRCh38 chr4: 122,841,913-122,841,913 , GRCh37.p13 chr4: 123,763,068-123,763,068 FGF2
    nsv5683920mobile element insertion2nstd211human GRCh38 chr4: 122,875,444-122,875,444 , GRCh37.p13 chr4: 123,796,599-123,796,599 FGF2
    nsv5675708mobile element insertion1nstd211human GRCh38 chr4: 122,861,887-122,861,887 , GRCh37.p13 chr4: 123,783,042-123,783,042 FGF2
    nsv5673739copy number variation1nstd102humanPathogenic GRCh37 chr4: 123,663,028-124,235,239 , GRCh38.p12 chr4: 122,741,873-123,314,084 FGF2, NUDT6, 5 more genes
    nsv5608621insertion1nstd207human GRCh38 chr4: 122,875,427-122,875,427 , GRCh37.p13 chr4: 123,796,582-123,796,582 FGF2
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5558253sequence alteration1nstd206human GRCh38 chr4: 120,373,769-143,797,136 , GRCh37.p13 chr4: 121,294,924-144,718,289 , IL15, 218 more genes
    nsv5544671insertion1nstd206human GRCh38 chr4: 122,861,887-122,861,923 , GRCh37.p13 chr4: 123,783,042-123,783,078 FGF2
    nsv5408951mobile element insertion1nstd206human GRCh38 chr4: 122,875,427-122,875,427 , GRCh37.p13 chr4: 123,796,582-123,796,582 FGF2
    nsv5404678mobile element insertion1nstd206human GRCh38 chr4: 122,841,913-122,841,964 , GRCh37.p13 chr4: 123,763,068-123,763,119 FGF2
    nsv5381774copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,833,638-130,232,122 , GRCh38.p12 chr4: 115,912,482-129,310,967 LOC112268469, LOC105377393, 159 more genes
    nsv5330303translocation1nstd200human GRCh37 chr12: 44,180,794-44,180,794 , GRCh37 chr4: 123,748,108-123,748,108 , GRCh38.p12 chr12: 43,786,991-43,786,991 , GRCh38.p12 chr4: 122,826,953-122,826,953 IRAK4, FGF2
    nsv5325236translocation1nstd204human GRCh37.p13 chr12: 44,180,794-44,180,794 , GRCh37.p13 chr4: 123,748,108-123,748,108 , GRCh38.p13 chr12: 43,786,991-43,786,991 , GRCh38.p13 chr4: 122,826,953-122,826,953 FGF2, IRAK4
    nsv5237674copy number variation1nstd204human GRCh38.p13 chr4: 122,892,085-122,893,308 , GRCh37.p13 chr4: 123,813,240-123,814,463 FGF2, NUDT6
    nsv5232889copy number variation1nstd204human GRCh38.p13 chr4: 122,892,209-122,897,441 , GRCh37.p13 chr4: 123,813,364-123,818,596 NUDT6, FGF2
    nsv5097820mobile element insertion1nstd203human GRCh38 chr4: 122,875,425-122,875,444 , GRCh37.p13 chr4: 123,796,580-123,796,599 FGF2
    nsv5095191mobile element insertion1nstd203human GRCh38 chr4: 122,875,434-122,875,444 , GRCh37.p13 chr4: 123,796,589-123,796,599 FGF2
    nsv5091514mobile element insertion1nstd203human GRCh38 chr4: 122,841,895-122,841,913 , GRCh37.p13 chr4: 123,763,050-123,763,068 FGF2
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