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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969692insertion1nstd209human GRCh38 chr16: 14,243,864-14,243,864 , GRCh37.p13 chr16: 14,337,721-14,337,721 MRTFB
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5945612copy number variation1nstd209human GRCh38 chr16: 14,245,266-14,246,735 , GRCh37.p13 chr16: 14,339,123-14,340,592 MRTFB
    nsv5943139copy number variation1nstd209human GRCh38 chr16: 14,001,632-14,082,581 , GRCh37.p13 chr16: 14,095,489-14,176,438 LINC02186, MRTFB, 1 more genes
    nsv5927995copy number variation1nstd209human GRCh38 chr16: 14,184,961-14,199,382 , GRCh37.p13 chr16: 14,278,818-14,293,239 TVP23CP2, MRTFB
    nsv5879108copy number variation1nstd209human GRCh38 chr16: 14,184,932-14,199,115 , GRCh37.p13 chr16: 14,278,789-14,292,972 MRTFB, TVP23CP2
    nsv5726821mobile element insertion1nstd211human GRCh38 chr16: 14,102,341-14,102,341 , GRCh37.p13 chr16: 14,196,198-14,196,198 MRTFB
    nsv5711448mobile element insertion1nstd211human GRCh38 chr16: 14,143,526-14,143,526 , GRCh37.p13 chr16: 14,237,383-14,237,383 MRTFB
    nsv5710135mobile element insertion1nstd211human GRCh38 chr16: 14,143,243-14,143,243 , GRCh37.p13 chr16: 14,237,100-14,237,100 MRTFB
    nsv5709954mobile element insertion1nstd211human GRCh38 chr16: 14,127,912-14,127,912 , GRCh37.p13 chr16: 14,221,769-14,221,769 MRTFB
    nsv5709688mobile element insertion1nstd211human GRCh38 chr16: 14,227,967-14,227,967 , GRCh37.p13 chr16: 14,321,824-14,321,824 MRTFB
    nsv5708396mobile element insertion2nstd211human GRCh38 chr16: 14,222,901-14,222,901 , GRCh37.p13 chr16: 14,316,758-14,316,758 MRTFB
    nsv5697681mobile element insertion1nstd211human GRCh38 chr16: 14,185,810-14,185,810 , GRCh37.p13 chr16: 14,279,667-14,279,667 MRTFB
    nsv5558886mobile element insertion1nstd206human GRCh38 chr16: 14,102,341-14,102,392 , GRCh37.p13 chr16: 14,196,198-14,196,249 MRTFB
    nsv5554796sequence alteration1nstd206human GRCh38 chr16: 14,245,267-14,245,277 , GRCh37.p13 chr16: 14,339,124-14,339,134 MRTFB
    nsv5544098insertion1nstd206human GRCh38 chr16: 14,245,267-14,245,267 , GRCh37.p13 chr16: 14,339,124-14,339,124 MRTFB
    nsv5538839insertion1nstd206human GRCh38 chr16: 14,106,904-14,106,955 , GRCh37.p13 chr16: 14,200,761-14,200,812 MRTFB
    nsv5524326copy number variation1nstd206human GRCh38 chr16: 14,067,413-14,069,198 , GRCh37.p13 chr16: 14,161,270-14,163,055 MRTFB
    nsv5516790copy number variation1nstd206human GRCh38 chr16: 14,240,955-14,243,586 , GRCh37.p13 chr16: 14,334,812-14,337,443 MRTFB
    nsv5427152mobile element insertion1nstd206human GRCh38 chr16: 14,185,810-14,185,861 , GRCh37.p13 chr16: 14,279,667-14,279,718 MRTFB
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