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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073834inversion1nstd229human GRCh38 chr20: 39,260,815-44,460,004 , GRCh37.p13 chr20: 37,889,458-43,088,644 LOC100128988, LOC100419859, 72 more genes
    nsv7062736inversion1nstd229human GRCh38 chr20: 36,955,253-45,585,462 , GRCh37.p13 chr20: 35,583,656-44,214,101 GDAP1L1, PI3, 177 more genes
    nsv7032846copy number variation1nstd229human GRCh38 chr20: 40,706,487-40,706,865 , GRCh37.p13 chr20: 39,335,127-39,335,505 LOC101927098
    nsv7026854copy number variation1nstd229human GRCh38 chr20: 39,412,497-41,213,411 , GRCh37.p13 chr20: 38,041,140-39,842,051 LOC105372616, LINC01370, 22 more genes
    nsv7021198copy number variation1nstd229human GRCh38 chr20: 33,145,032-41,995,765 , GRCh37.p13 chr20: 31,732,838-40,624,405 PXMP4, RPL12P11, 199 more genes
    nsv6596116inversion1nstd223human GRCh38 chr20: 36,955,253-45,585,469 , GRCh37.p13 chr20: 35,583,656-44,214,108 LOC101929863, LOC105372620, 177 more genes
    nsv6134292copy number variation1nstd213human GRCh37 chr20: 38,940,000-39,600,001 , GRCh38.p12 chr20: 40,311,360-40,971,361 MAFB, RNA5SP484, 7 more genes
    nsv6134027copy number variation1nstd213human GRCh37 chr20: 38,860,000-39,330,001 , GRCh38.p12 chr20: 40,231,360-40,701,361 MAFB, LOC101927098, 5 more genes
    nsv6134025copy number variation1nstd213human GRCh37 chr20: 37,530,000-39,510,001 , GRCh38.p12 chr20: 38,901,357-40,881,361 LINC01734, LOC102724950, 21 more genes
    nsv5976704inversion1nstd209human GRCh38 chr20: 36,955,252-45,585,469 , GRCh37.p13 chr20: 35,583,655-44,214,108 , ADA, 180 more genes
    nsv5951164copy number variation1nstd209human GRCh38 chr20: 40,701,511-40,702,664 , GRCh37.p13 chr20: 39,330,151-39,331,304 LOC101927098
    nsv5324090inversion1nstd204human GRCh37.p13 chr20: 35,583,652-44,214,109 , GRCh38.p13 chr20: 36,955,249-45,585,470 , BPI, 180 more genes
    nsv5033948inversion1nstd200human GRCh38 chr20: 36,955,253-45,585,464 , GRCh37.p13 chr20: 35,583,656-44,214,103 , EMILIN3, 180 more genes
    nsv5022343copy number variation1nstd200human GRCh38 chr20: 32,602,560-45,347,064 , GRCh37.p13 chr20: 31,190,362-43,975,704 , SNHG11, 286 more genes
    nsv5022342copy number variation1nstd200human GRCh38 chr20: 32,576,247-46,538,786 , GRCh37.p13 chr20: 31,164,049-45,167,425 , NECAB3, 350 more genes
    nsv5022326copy number variation1nstd200human GRCh38 chr20: 32,216,214-44,981,731 , GRCh37.p13 chr20: 30,804,017-43,610,372 , HNF4A, 279 more genes
    nsv4884257inversion1nstd200human GRCh37 chr20: 35,583,656-44,214,103 , GRCh38.p12 chr20: 36,955,253-45,585,464 , TGM2, 180 more genes
    nsv4868593copy number variation1nstd200human GRCh37 chr20: 31,164,049-45,167,425 , GRCh38.p12 chr20: 32,576,247-46,538,786 , MMP24-AS1-EDEM2, 350 more genes
    nsv4868578copy number variation1nstd200human GRCh37 chr20: 30,804,017-43,610,372 , GRCh38.p12 chr20: 32,216,214-44,981,731 , SNORA71C, 279 more genes
    nsv4674805copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 34,980,430-46,806,549 , GRCh38.p12 chr20: 36,352,027-48,177,806 ADA, BPI, 266 more genes
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