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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5887135copy number variation1nstd209human GRCh38 chr1: 108,930,496-108,930,626 , GRCh37.p13 chr1: 109,473,118-109,473,248 GPSM2, CLCC1
    nsv5878668copy number variation1nstd209human GRCh38 chr1: 108,928,010-108,928,072 , GRCh37.p13 chr1: 109,470,632-109,470,694 GPSM2, CLCC1
    nsv5870274copy number variation1nstd209human GRCh38 chr1: 108,900,422-108,901,588 , GRCh37.p13 chr1: 109,443,044-109,444,210 GPSM2
    nsv5827593copy number variation1nstd209human GRCh38 chr1: 108,900,298-108,901,697 , GRCh37.p13 chr1: 109,442,920-109,444,319 GPSM2
    nsv5685643mobile element insertion1nstd211human GRCh38 chr1: 108,886,328-108,886,328 , GRCh37.p13 chr1: 109,428,950-109,428,950 GPSM2
    nsv5623152insertion1nstd207human GRCh38 chr1: 108,933,209-108,933,209 , GRCh37.p13 chr1: 109,475,831-109,475,831 GPSM2, CLCC1
    nsv5615825insertion1nstd207human GRCh38 chr1: 108,908,728-108,908,728 , GRCh37.p13 chr1: 109,451,350-109,451,350 GPSM2
    nsv5583804copy number variation1nstd207human GRCh38 chr1: 108,930,496-108,930,626 , GRCh37.p13 chr1: 109,473,118-109,473,248 GPSM2, CLCC1
    nsv5577585copy number variation1nstd207human GRCh38 chr1: 108,933,081-108,933,226 , GRCh37.p13 chr1: 109,475,703-109,475,848 CLCC1, GPSM2
    nsv5576426copy number variation1nstd207human GRCh38 chr1: 108,873,383-108,873,449 , GRCh37.p13 chr1: 109,416,005-109,416,071 , GPSM2
    nsv5536523insertion1nstd206human GRCh38 chr1: 108,908,738-108,908,779 , GRCh37.p13 chr1: 109,451,360-109,451,401 GPSM2
    nsv5424057copy number variation1nstd206human GRCh38 chr1: 108,930,522-108,930,627 , GRCh37.p13 chr1: 109,473,144-109,473,249 CLCC1, GPSM2
    nsv5419869copy number variation1nstd206human GRCh38 chr1: 108,842,219-108,891,126 , GRCh37.p13 chr1: 109,384,841-109,433,748 , SPATA42, 2 more genes
    nsv5415050copy number variation1nstd206human GRCh38 chr1: 108,866,569-108,915,310 , GRCh37.p13 chr1: 109,409,191-109,457,932 , GPSM2
    nsv5381125copy number variation1nstd102humanUncertain significance GRCh37 chr1: 109,428,145-109,816,671 , GRCh38.p12 chr1: 108,885,523-109,274,049 SCARNA2, RANP5, 15 more genes
    nsv5381058copy number variation1nstd102humanPathogenic GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855 AMYP1, MIR4256, 320 more genes
    nsv5298141copy number variation1nstd204human GRCh38.p13 chr1: 108,723,191-109,333,704 , GRCh37.p13 chr1: 109,265,813-109,876,326 , SARS1, 25 more genes
    nsv5298075copy number variation1nstd204human GRCh38.p13 chr1: 108,904,731-108,981,556 , GRCh37.p13 chr1: 109,447,353-109,524,178 WDR47, GPSM2, 1 more genes
    nsv5220364copy number variation1nstd204human GRCh38.p13 chr1: 108,904,401-108,981,500 , GRCh37.p13 chr1: 109,447,023-109,524,122 WDR47, CLCC1, 1 more genes
    nsv5218257copy number variation1nstd204human GRCh37.p13 chr1: 109,315,123-109,468,222 , GRCh38.p13 chr1: 108,772,501-108,925,600 , STXBP3, 4 more genes
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