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Items: 1 to 20 of 357

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976013insertion1nstd209human GRCh38 chr11: 110,687,056-110,687,056 , GRCh37.p13 chr11: 110,557,779-110,557,779 ARHGAP20
    nsv5924804copy number variation1nstd209human GRCh38 chr11: 110,618,753-110,619,266 , GRCh37.p13 chr11: 110,489,477-110,489,990 ARHGAP20
    nsv5857684copy number variation1nstd209human GRCh38 chr11: 110,664,498-110,665,597 , GRCh37.p13 chr11: 110,535,221-110,536,320 ARHGAP20
    nsv5727418mobile element insertion1nstd211human GRCh38 chr11: 110,658,792-110,658,792 , GRCh37.p13 chr11: 110,529,515-110,529,515 ARHGAP20
    nsv5716176mobile element insertion1nstd211human GRCh38 chr11: 110,660,075-110,660,075 , GRCh37.p13 chr11: 110,530,798-110,530,798 ARHGAP20
    nsv5710582mobile element insertion2nstd211human GRCh38 chr11: 110,689,594-110,689,594 , GRCh37.p13 chr11: 110,560,317-110,560,317 ARHGAP20
    nsv5709163mobile element insertion1nstd211human GRCh38 chr11: 110,675,894-110,675,894 , GRCh37.p13 chr11: 110,546,617-110,546,617 ARHGAP20
    nsv5706888mobile element insertion1nstd211human GRCh38 chr11: 110,649,183-110,649,183 , GRCh37.p13 chr11: 110,519,906-110,519,906 ARHGAP20
    nsv5695725mobile element insertion1nstd211human GRCh38 chr11: 110,602,883-110,602,883 , GRCh37.p13 chr11: 110,473,607-110,473,607 ARHGAP20
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5602419copy number variation1nstd207human GRCh38 chr11: 110,618,671-110,618,900 , GRCh37.p13 chr11: 110,489,395-110,489,624 ARHGAP20
    nsv5602374copy number variation1nstd207human GRCh38 chr11: 110,618,654-110,619,130 , GRCh37.p13 chr11: 110,489,378-110,489,854 ARHGAP20
    nsv5590466copy number variation1nstd207human GRCh38 chr11: 110,619,252-110,619,330 , GRCh37.p13 chr11: 110,489,976-110,490,054 ARHGAP20
    nsv5589423copy number variation1nstd207human GRCh38 chr11: 110,648,194-110,648,253 , GRCh37.p13 chr11: 110,518,917-110,518,976 ARHGAP20
    nsv5509179copy number variation1nstd206human GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687 , ATM, 153 more genes
    nsv5507847copy number variation1nstd206human GRCh38 chr11: 110,577,243-110,577,299 , GRCh37.p13 chr11: 110,447,967-110,448,023 ARHGAP20
    nsv5431816mobile element insertion1nstd206human GRCh38 chr11: 110,602,883-110,602,934 , GRCh37.p13 chr11: 110,473,607-110,473,658 ARHGAP20
    nsv5426224mobile element insertion1nstd206human GRCh38 chr11: 110,675,894-110,675,945 , GRCh37.p13 chr11: 110,546,617-110,546,668 ARHGAP20
    nsv5417955mobile element insertion1nstd206human GRCh38 chr11: 110,689,594-110,689,625 , GRCh37.p13 chr11: 110,560,317-110,560,348 ARHGAP20
    nsv5389547copy number variation1nstd186human GRCh37 chr11: 110,489,664-110,489,953 , GRCh38.p12 chr11: 110,618,940-110,619,229 ARHGAP20
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