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Items: 1 to 20 of 196

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5869303copy number variation1nstd209human GRCh38 chr1: 200,641,480-200,641,739 , GRCh37.p13 chr1: 200,610,608-200,610,867 DDX59
    nsv5829153copy number variation1nstd209human GRCh38 chr1: 200,632,629-200,640,226 , GRCh37.p13 chr1: 200,601,757-200,609,354 DDX59
    nsv5829080copy number variation1nstd209human GRCh38 chr1: 200,654,200-200,657,308 , GRCh37.p13 chr1: 200,623,328-200,626,436 DDX59
    nsv5446509copy number variation1nstd206human GRCh38 chr1: 200,667,214-200,668,095 , GRCh37.p13 chr1: 200,636,342-200,637,223 DDX59-AS1, DDX59
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5291438copy number variation1nstd204human GRCh38.p13 chr1: 200,654,253-200,657,542 , GRCh37.p13 chr1: 200,623,381-200,626,670 DDX59
    nsv5218291copy number variation1nstd204human GRCh38.p13 chr1: 200,654,200-200,657,558 , GRCh37.p13 chr1: 200,623,328-200,626,686 DDX59
    nsv5212043mobile element deletion1nstd204human GRCh38.p13 chr1: 200,641,471-200,641,733 , GRCh37.p13 chr1: 200,610,599-200,610,861 DDX59
    nsv5202535copy number variation1nstd204human GRCh38.p13 chr1: 200,651,001-200,657,600 , GRCh37.p13 chr1: 200,620,129-200,626,728 DDX59
    nsv4904241copy number variation1nstd200human GRCh38 chr1: 200,618,317-200,816,820 , GRCh37.p13 chr1: 200,587,445-200,785,948 DDX59-AS1, DDX59, 2 more genes
    nsv4774096mobile element deletion1nstd200human GRCh37 chr1: 200,610,608-200,610,858 , GRCh38.p12 chr1: 200,641,480-200,641,730 DDX59
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4685577copy number variation1nstd102humannot provided GRCh37 chr1: 194,356,425-210,988,710 , GRCh38.p12 chr1: 194,387,295-210,815,368 SEPTIN14P12, LINC02602, 332 more genes
    nsv4679918copy number variation1nstd189human GRCh37.p13 chr1: 200,578,042-200,907,372 , GRCh38.p12 chr1: 200,608,914-200,938,244 , GPR25, 8 more genes
    nsv4594220copy number variation1nstd183human GRCh37 chr1: 200,638,822-200,639,021 , GRCh38.p12 chr1: 200,669,694-200,669,893 DDX59, DDX59-AS1
    nsv4580090copy number variation1nstd183human GRCh37 chr1: 200,623,544-200,624,376 , GRCh38.p12 chr1: 200,654,416-200,655,248 DDX59
    nsv4516537copy number variation1nstd166human GRCh37.p13 chr1: 200,587,598-200,863,000 , GRCh38.p12 chr1: 200,618,470-200,893,872 , GPR25, 6 more genes
    nsv4459897mobile element insertion1nstd166human GRCh37.p13 chr1: 200,616,591-200,616,591 , GRCh38.p12 chr1: 200,647,463-200,647,463 DDX59
    nsv4452272copy number variation1nstd102humanUncertain significance GRCh37 chr1: 200,575,876-200,784,156 , GRCh38.p12 chr1: 200,606,748-200,815,028 DDX59-AS1, DDX59, 2 more genes
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