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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112736copy number variation1nstd102humanPathogenic GRCh37 chr10: 48,301,535-51,807,296 , GRCh38.p12 chr10: 45,999,930-49,959,916 SHLD2P3, LOC100420617, 95 more genes
    nsv5925565copy number variation1nstd209human GRCh38 chr10: 49,100,215-49,100,321 , GRCh37.p13 chr10: 50,308,260-50,308,366 VSTM4
    nsv5924861copy number variation1nstd209human GRCh38 chr10: 49,127,173-49,127,231 , GRCh37.p13 chr10: 50,335,218-50,335,276 VSTM4, FAM170B-AS1
    nsv5918225copy number variation1nstd209human GRCh38 chr10: 49,062,335-49,062,428 , GRCh37.p13 chr10: 50,270,380-50,270,473 VSTM4
    nsv5916113copy number variation1nstd209human GRCh38 chr10: 45,791,488-50,132,032 , GRCh37.p13 chr10|NW_003871068.1: 62,603-2,281,126 , GRCh37.p13 chr10: 46,591,857-51,891,792 , LINC02675, 111 more genes
    nsv5914502copy number variation1nstd209human GRCh38 chr10: 45,768,833-50,109,449 , GRCh37.p13 chr10: 46,591,857-51,028,871 , GRCh37.p13 chr10|NW_003871068.1: 39,948-2,281,126 , AGAP13P, 111 more genes
    nsv5847925copy number variation1nstd209human GRCh38 chr10: 49,025,200-49,027,492 , GRCh37.p13 chr10: 50,233,245-50,235,537 VSTM4
    nsv5726430mobile element insertion2nstd211human GRCh38 chr10: 49,021,167-49,021,167 , GRCh37.p13 chr10: 50,229,212-50,229,212 VSTM4
    nsv5601490copy number variation1nstd207human GRCh38 chr10: 49,069,970-49,070,286 , GRCh37.p13 chr10: 50,278,015-50,278,331 VSTM4
    nsv5599899copy number variation1nstd207human GRCh38 chr10: 49,127,173-49,127,231 , GRCh37.p13 chr10: 50,335,218-50,335,276 VSTM4, FAM170B-AS1
    nsv5591887copy number variation1nstd207human GRCh38 chr10: 49,125,132-49,125,208 , GRCh37.p13 chr10: 50,333,177-50,333,253 FAM170B-AS1, VSTM4
    nsv5489064copy number variation1nstd206human GRCh38 chr10: 49,062,339-49,062,429 , GRCh37.p13 chr10: 50,270,384-50,270,474 VSTM4
    nsv5488820copy number variation1nstd206human GRCh38 chr10: 49,114,257-49,130,180 , GRCh37.p13 chr10: 50,322,302-50,338,225 FAM170B-AS1, VSTM4, 1 more genes
    nsv5486004copy number variation1nstd206human GRCh38 chr10: 49,069,970-49,070,272 , GRCh37.p13 chr10: 50,278,015-50,278,317 VSTM4
    nsv5484930copy number variation1nstd206human GRCh38 chr10: 49,011,906-49,038,632 , GRCh37.p13 chr10: 50,219,951-50,246,677 VSTM4
    nsv5483515copy number variation1nstd206human GRCh38 chr10: 47,586,000-50,754,368 , GRCh37.p13 chr10: 46,591,857-52,514,128 HMGB1P50, PARG, 65 more genes
    nsv5482918copy number variation1nstd206human GRCh38 chr10: 48,676,996-49,241,090 , GRCh37.p13 chr10: 49,885,041-50,449,135 FAM170B-AS1, LRRC18, 8 more genes
    nsv5476043copy number variation1nstd206human GRCh38 chr10: 49,100,215-49,100,323 , GRCh37.p13 chr10: 50,308,260-50,308,368 VSTM4
    nsv5475483copy number variation1nstd206human GRCh38 chr10: 49,110,357-49,111,748 , GRCh37.p13 chr10: 50,318,402-50,319,793 VSTM4
    nsv5475009copy number variation1nstd206human GRCh38 chr10: 49,125,133-49,125,214 , GRCh37.p13 chr10: 50,333,178-50,333,259 VSTM4, FAM170B-AS1
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