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Items: 1 to 20 of 306

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5951226insertion1nstd209human GRCh38 chr6: 36,429,253-36,429,253 , GRCh37.p13 chr6: 36,397,030-36,397,030 PXT1
    nsv5903814copy number variation1nstd209human GRCh38 chr6: 36,398,021-36,398,303 , GRCh37.p13 chr6: 36,365,798-36,366,080 PXT1
    nsv5902609copy number variation1nstd209human GRCh38 chr6: 36,409,863-36,410,135 , GRCh37.p13 chr6: 36,377,640-36,377,912 PXT1
    nsv5893260copy number variation1nstd209human GRCh38 chr6: 36,412,232-36,413,320 , GRCh37.p13 chr6: 36,380,009-36,381,097 PXT1
    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
    nsv5719324mobile element insertion2nstd211human GRCh38 chr6: 36,420,024-36,420,024 , GRCh37.p13 chr6: 36,387,801-36,387,801 PXT1
    nsv5680673mobile element insertion2nstd211human GRCh38 chr6: 36,400,068-36,400,068 , GRCh37.p13 chr6: 36,367,845-36,367,845 PXT1
    nsv5628438insertion1nstd207human GRCh38 chr6: 36,429,253-36,429,253 , GRCh37.p13 chr6: 36,397,030-36,397,030 PXT1
    nsv5552142insertion1nstd206human GRCh38 chr6: 36,429,270-36,429,270 , GRCh37.p13 chr6: 36,397,047-36,397,047 PXT1
    nsv5471022copy number variation1nstd206human GRCh38 chr6: 36,411,230-36,413,246 , GRCh37.p13 chr6: 36,379,007-36,381,023 PXT1
    nsv5466088copy number variation1nstd206human GRCh38 chr6: 36,417,165-36,423,571 , GRCh37.p13 chr6: 36,384,942-36,391,348 PXT1
    nsv5464670copy number variation1nstd206human GRCh38 chr6: 36,398,024-36,398,304 , GRCh37.p13 chr6: 36,365,801-36,366,081 PXT1
    nsv5458756copy number variation1nstd206human GRCh38 chr6: 36,417,525-36,417,694 , GRCh37.p13 chr6: 36,385,302-36,385,471 PXT1
    nsv5458279copy number variation1nstd206human GRCh38 chr6: 36,436,675-36,436,758 , GRCh37.p13 chr6: 36,404,452-36,404,535 PXT1
    nsv5411183mobile element insertion1nstd206human GRCh38 chr6: 36,400,068-36,400,119 , GRCh37.p13 chr6: 36,367,845-36,367,896 PXT1
    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
    nsv5190373mobile element insertion1nstd203human GRCh38 chr6: 36,420,014-36,420,024 , GRCh37.p13 chr6: 36,387,791-36,387,801 PXT1
    nsv5119964mobile element insertion1nstd203human GRCh38 chr6: 36,429,256-36,429,285 , GRCh37.p13 chr6: 36,397,033-36,397,062 PXT1
    nsv5119918mobile element insertion1nstd203human GRCh38 chr6: 36,429,231-36,429,253 , GRCh37.p13 chr6: 36,397,008-36,397,030 PXT1
    nsv5119533mobile element insertion1nstd203human GRCh38 chr6: 36,428,400-36,428,416 , GRCh37.p13 chr6: 36,396,177-36,396,193 PXT1
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