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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962184insertion1nstd209human GRCh38 chr10: 27,028,585-27,028,585 , GRCh37.p13 chr10: 27,317,514-27,317,514 ANKRD26
    nsv5953965insertion1nstd209human GRCh38 chr10: 26,951,017-26,951,017 , GRCh37.p13 chr10: 27,239,946-27,239,946 ANKRD26
    nsv5915471copy number variation1nstd209human GRCh38 chr10: 26,935,271-26,939,155 , GRCh37.p13 chr10: 27,224,200-27,228,084 ANKRD26, FAM238C
    nsv5908775copy number variation1nstd209human GRCh38 chr10: 26,935,698-26,940,377 , GRCh37.p13 chr10: 27,224,627-27,229,306 ANKRD26, FAM238C
    nsv5862659copy number variation3nstd209human GRCh38 chr10: 26,935,454-26,937,564 , GRCh37.p13 chr10: 27,224,383-27,226,493 ANKRD26, FAM238C
    nsv5726404mobile element insertion1nstd211human GRCh38 chr10: 27,095,280-27,095,280 , GRCh37.p13 chr10: 27,384,209-27,384,209 ANKRD26
    nsv5710879mobile element insertion1nstd211human GRCh38 chr10: 26,965,053-26,965,053 , GRCh37.p13 chr10: 27,253,982-27,253,982 ANKRD26
    nsv5705164mobile element insertion1nstd211human GRCh38 chr10: 27,021,883-27,021,883 , GRCh37.p13 chr10: 27,310,812-27,310,812 ANKRD26
    nsv5701557mobile element insertion2nstd211human GRCh38 chr10: 26,938,146-26,938,146 , GRCh37.p13 chr10: 27,227,075-27,227,075 ANKRD26, FAM238C
    nsv5701460mobile element insertion1nstd211human GRCh38 chr10: 27,082,074-27,082,074 , GRCh37.p13 chr10: 27,371,003-27,371,003 ANKRD26
    nsv5592557copy number variation1nstd207human GRCh38 chr10: 26,935,271-26,939,155 , GRCh37.p13 chr10: 27,224,200-27,228,084 FAM238C, ANKRD26
    nsv5487037copy number variation1nstd206human GRCh38 chr10: 26,980,114-26,980,579 , GRCh37.p13 chr10: 27,269,043-27,269,508 ANKRD26
    nsv5486953copy number variation1nstd206human GRCh38 chr10: 27,054,872-27,054,993 , GRCh37.p13 chr10: 27,343,801-27,343,922 ANKRD26
    nsv5485777copy number variation1nstd206human GRCh38 chr10: 27,096,406-27,106,986 , GRCh37.p13 chr10: 27,385,335-27,395,915 ANKRD26
    nsv5484262copy number variation1nstd206human GRCh38 chr10: 26,935,678-26,940,398 , GRCh37.p13 chr10: 27,224,607-27,229,327 FAM238C, ANKRD26
    nsv5483050copy number variation1nstd206human GRCh38 chr10: 27,042,537-27,369,512 , GRCh37.p13 chr10: 27,331,466-27,658,441 RNU6-666P, ANKRD26, 12 more genes
    nsv5479497copy number variation1nstd206human GRCh38 chr10: 26,970,845-26,971,558 , GRCh37.p13 chr10: 27,259,774-27,260,487 ANKRD26
    nsv5475996copy number variation1nstd206human GRCh38 chr10: 27,099,810-27,100,333 , GRCh37.p13 chr10: 27,388,739-27,389,262 ANKRD26
    nsv5409062mobile element insertion1nstd206human GRCh38 chr10: 26,965,053-26,965,104 , GRCh37.p13 chr10: 27,253,982-27,254,033 ANKRD26
    nsv5395640mobile element insertion1nstd206human GRCh38 chr10: 27,021,883-27,021,934 , GRCh37.p13 chr10: 27,310,812-27,310,863 ANKRD26
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