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Items: 1 to 20 of 282

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5956970insertion1nstd209human GRCh38 chr6: 36,053,991-36,053,991 , GRCh37.p13 chr6: 36,021,768-36,021,768 MAPK14
    nsv5898635copy number variation1nstd209human GRCh38 chr6: 36,102,342-36,102,415 , GRCh37.p13 chr6: 36,070,119-36,070,192 MAPK14
    nsv5892330copy number variation1nstd209human GRCh38 chr6: 35,948,470-36,584,214 , GRCh37.p13 chr6: 35,916,247-36,551,991 SLC26A8, STK38, 17 more genes
    nsv5717470mobile element insertion2nstd211human GRCh38 chr6: 36,029,356-36,029,356 , GRCh37.p13 chr6: 35,997,133-35,997,133 MAPK14
    nsv5684202mobile element insertion1nstd211human GRCh38 chr6: 36,067,951-36,067,951 , GRCh37.p13 chr6: 36,035,728-36,035,728 MAPK14
    nsv5674774mobile element insertion2nstd211human GRCh38 chr6: 36,054,007-36,054,007 , GRCh37.p13 chr6: 36,021,784-36,021,784 MAPK14
    nsv5642843insertion1nstd207human GRCh38 chr6: 36,029,871-36,029,871 , GRCh37.p13 chr6: 35,997,648-35,997,648 MAPK14
    nsv5634512insertion1nstd207human GRCh38 chr6: 36,053,991-36,053,991 , GRCh37.p13 chr6: 36,021,768-36,021,768 MAPK14
    nsv5575026copy number variation1nstd207human GRCh38 chr6: 36,102,342-36,102,415 , GRCh37.p13 chr6: 36,070,119-36,070,192 MAPK14
    nsv5458897copy number variation1nstd206human GRCh38 chr6: 36,102,343-36,102,416 , GRCh37.p13 chr6: 36,070,120-36,070,193 MAPK14
    nsv5406207mobile element insertion1nstd206human GRCh38 chr6: 36,067,951-36,067,991 , GRCh37.p13 chr6: 36,035,728-36,035,768 MAPK14
    nsv5402380mobile element insertion1nstd206human GRCh38 chr6: 36,054,007-36,054,058 , GRCh37.p13 chr6: 36,021,784-36,021,835 MAPK14
    nsv5362856translocation1nstd200human GRCh38 chr6: 36,102,416-36,102,416 , GRCh38 chr6: 36,102,343-36,102,343 , GRCh37.p13 chr6: 36,070,193-36,070,193 , GRCh37.p13 chr6: 36,070,120-36,070,120 MAPK14
    nsv5322216translocation1nstd204human GRCh38.p13 chr6: 36,102,416-36,102,416 , GRCh38.p13 chr6: 36,102,343-36,102,343 , GRCh37.p13 chr6: 36,070,120-36,070,120 , GRCh37.p13 chr6: 36,070,193-36,070,193 MAPK14
    nsv5239912copy number variation1nstd204human GRCh38.p13 chr6: 36,115,901-36,129,900 , GRCh37.p13 chr6: 36,083,678-36,097,677 MAPK13, MAPK14
    nsv5200371copy number variation1nstd102humanPathogenic GRCh37 chr6: 34,401,304-38,435,497 , GRCh38.p12 chr6: 34,433,527-38,467,721 RPS15AP19, FKBP5, 95 more genes
    nsv5119839mobile element insertion1nstd203human GRCh38 chr6: 36,053,991-36,054,004 , GRCh37.p13 chr6: 36,021,768-36,021,781 MAPK14
    nsv5119391mobile element insertion1nstd203human GRCh38 chr6: 36,089,660-36,089,676 , GRCh37.p13 chr6: 36,057,437-36,057,453 MAPK14, NUDT5P1
    nsv5116059mobile element insertion1nstd203human GRCh38 chr6: 36,053,994-36,054,007 , GRCh37.p13 chr6: 36,021,771-36,021,784 MAPK14
    nsv5113023mobile element insertion1nstd203human GRCh38 chr6: 36,053,997-36,054,007 , GRCh37.p13 chr6: 36,021,774-36,021,784 MAPK14
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