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Items: 1 to 20 of 883

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6120392copy number variation1nstd186human GRCh37 chr6: 89,424,166-89,424,460 , GRCh38.p12 chr6: 88,714,447-88,714,741 RNGTT
    nsv5966720insertion1nstd209human GRCh38 chr6: 88,647,701-88,647,701 , GRCh37.p13 chr6: 89,357,420-89,357,420 RNGTT
    nsv5964996insertion1nstd209human GRCh38 chr6: 88,930,168-88,930,168 , GRCh37.p13 chr6: 89,639,887-89,639,887 RNGTT
    nsv5956326insertion1nstd209human GRCh38 chr6: 88,647,984-88,647,984 , GRCh37.p13 chr6: 89,357,703-89,357,703 RNGTT
    nsv5950860insertion1nstd209human GRCh38 chr6: 88,686,907-88,686,907 , GRCh37.p13 chr6: 89,396,626-89,396,626 RNGTT
    nsv5905888copy number variation1nstd209human GRCh38 chr6: 88,880,769-88,880,865 , GRCh37.p13 chr6: 89,590,488-89,590,584 RNGTT
    nsv5904989copy number variation1nstd209human GRCh38 chr6: 88,781,475-88,782,595 , GRCh37.p13 chr6: 89,491,194-89,492,314 RNGTT
    nsv5902087copy number variation1nstd209human GRCh38 chr6: 88,654,585-88,654,676 , GRCh37.p13 chr6: 89,364,304-89,364,395 RNGTT
    nsv5898679copy number variation1nstd209human GRCh38 chr6: 88,844,701-88,845,195 , GRCh37.p13 chr6: 89,554,420-89,554,914 RNGTT
    nsv5897812copy number variation1nstd209human GRCh38 chr6: 88,848,534-88,848,594 , GRCh37.p13 chr6: 89,558,253-89,558,313 RNGTT
    nsv5894517copy number variation1nstd209human GRCh38 chr6: 88,705,321-88,706,932 , GRCh37.p13 chr6: 89,415,040-89,416,651 RNGTT
    nsv5893440copy number variation1nstd209human GRCh38 chr6: 88,714,433-88,714,740 , GRCh37.p13 chr6: 89,424,152-89,424,459 RNGTT
    nsv5892689copy number variation1nstd209human GRCh38 chr6: 88,647,622-88,647,979 , GRCh37.p13 chr6: 89,357,341-89,357,698 RNGTT
    nsv5892304copy number variation1nstd209human GRCh38 chr6: 88,907,354-88,907,413 , GRCh37.p13 chr6: 89,617,073-89,617,132 RNGTT
    nsv5887654copy number variation1nstd209human GRCh38 chr6: 88,726,348-88,726,400 , GRCh37.p13 chr6: 89,436,067-89,436,119 RNGTT
    nsv5845812copy number variation2nstd209human GRCh38 chr6: 88,781,493-88,782,492 , GRCh37.p13 chr6: 89,491,212-89,492,211 RNGTT
    nsv5845810copy number variation1nstd209human GRCh38 chr6: 88,705,504-88,707,003 , GRCh37.p13 chr6: 89,415,223-89,416,722 RNGTT
    nsv5723847mobile element insertion1nstd211human GRCh38 chr6: 88,760,801-88,760,801 , GRCh37.p13 chr6: 89,470,520-89,470,520 RNGTT
    nsv5694054mobile element insertion2nstd211human GRCh38 chr6: 88,712,799-88,712,799 , GRCh37.p13 chr6: 89,422,518-89,422,518 RNGTT
    nsv5693980mobile element insertion1nstd211human GRCh38 chr6: 88,647,984-88,647,984 , GRCh37.p13 chr6: 89,357,703-89,357,703 RNGTT
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