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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976704inversion1nstd209human GRCh38 chr20: 36,955,252-45,585,469 , GRCh37.p13 chr20: 35,583,655-44,214,108 , ADA, 180 more genes
    nsv5706041mobile element insertion2nstd211human GRCh38 chr20: 44,479,428-44,479,428 , GRCh37.p13 chr20: 43,108,068-43,108,068 TTPAL
    nsv5350395translocation1nstd200human GRCh38 chr20: 44,490,584-44,490,584 , GRCh38 chr20: 44,490,658-44,490,658 , GRCh37.p13 chr20: 43,119,225-43,119,225 , GRCh37.p13 chr20: 43,119,299-43,119,299 TTPAL
    nsv5325566copy number variation1nstd204human GRCh38.p13 chr20: 44,248,826-44,533,449 , GRCh37.p13 chr20: 42,877,466-43,162,090 R3HDML, SERINC3, 11 more genes
    nsv5324090inversion1nstd204human GRCh37.p13 chr20: 35,583,652-44,214,109 , GRCh38.p13 chr20: 36,955,249-45,585,470 , BPI, 180 more genes
    nsv5290254copy number variation1nstd204human GRCh38.p13 chr20: 44,248,701-44,533,500 , GRCh37.p13 chr20: 42,877,341-43,162,141 FITM2, RPL37AP1, 11 more genes
    nsv5287202copy number variation1nstd204human GRCh38.p13 chr20: 44,492,344-44,533,448 , GRCh37.p13 chr20: 43,120,985-43,162,089 SERINC3, PKIG, 1 more genes
    nsv5285846copy number variation1nstd204human GRCh38.p13 chr20: 44,473,065-44,495,243 , GRCh37.p13 chr20: 43,101,705-43,123,884 SERINC3, TTPAL
    nsv5033948inversion1nstd200human GRCh38 chr20: 36,955,253-45,585,464 , GRCh37.p13 chr20: 35,583,656-44,214,103 , EMILIN3, 180 more genes
    nsv5025631copy number variation1nstd200human GRCh38 chr20: 44,248,833-44,533,440 , GRCh37.p13 chr20: 42,877,473-43,162,081 SERINC3, HNF4A, 11 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
    nsv4865585copy number variation1nstd200human GRCh37 chr20: 42,877,473-43,162,081 , GRCh38.p12 chr20: 44,248,833-44,533,440 SERINC3, HNF4A, 11 more genes
    nsv4853644copy number variation1nstd200human GRCh37 chr20: 43,120,071-43,120,371 , GRCh38.p12 chr20: 44,491,430-44,491,730 TTPAL
    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
    nsv4625716copy number variation1nstd183human GRCh37 chr20: 43,042,130-43,230,972 , GRCh38.p12 chr20: 44,413,490-44,602,331 HNF4A, SERINC3, 5 more genes
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