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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5922926copy number variation1nstd209human GRCh38 chr10: 93,785,720-93,786,737 , GRCh37.p13 chr10: 95,545,477-95,546,494 LOC105378437, LGI1
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5698361mobile element insertion1nstd211human GRCh38 chr10: 93,764,764-93,764,764 , GRCh37.p13 chr10: 95,524,521-95,524,521 LOC105378437, LGI1
    nsv5672611copy number variation1nstd102humanPathogenic GRCh37 chr10: 95,517,882-95,537,394 , GRCh38.p12 chr10: 93,758,125-93,777,637 LGI1, LOC101927013, 1 more genes
    nsv5593096copy number variation1nstd207human GRCh38 chr10: 93,785,720-93,786,713 , GRCh37.p13 chr10: 95,545,477-95,546,470 LGI1, LOC105378437
    nsv5537785insertion1nstd206human GRCh38 chr10: 93,761,766-93,761,797 , GRCh37.p13 chr10: 95,521,523-95,521,554 LOC105378437, LGI1
    nsv5481139copy number variation1nstd206human GRCh38 chr10: 93,781,124-93,783,278 , GRCh37.p13 chr10: 95,540,881-95,543,035 LOC105378437, LGI1
    nsv5476955copy number variation1nstd206human GRCh38 chr10: 93,785,720-93,786,738 , GRCh37.p13 chr10: 95,545,477-95,546,495 LGI1, LOC105378437
    nsv5401559mobile element insertion1nstd206human GRCh38 chr10: 93,764,764-93,764,815 , GRCh37.p13 chr10: 95,524,521-95,524,572 LGI1, LOC105378437
    nsv5315647copy number variation1nstd204human GRCh37.p13 chr10: 95,545,477-95,546,495 , GRCh38.p13 chr10: 93,785,720-93,786,738 LOC105378437, LGI1
    nsv5258490copy number variation1nstd204human GRCh38.p13 chr10: 93,785,701-93,786,700 , GRCh37.p13 chr10: 95,545,458-95,546,457 LGI1, LOC105378437
    nsv5128080mobile element insertion1nstd203human GRCh38 chr10: 93,766,512-93,766,522 , GRCh37.p13 chr10: 95,526,269-95,526,279 LOC105378437, LGI1
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4986726copy number variation1nstd200human GRCh38 chr10: 93,785,720-93,786,738 , GRCh37.p13 chr10: 95,545,477-95,546,495 LOC105378437, LGI1
    nsv4843401copy number variation1nstd200human GRCh37 chr10: 95,545,477-95,546,495 , GRCh38.p12 chr10: 93,785,720-93,786,738 LGI1, LOC105378437
    nsv4746435copy number variation1nstd199human GRCh37 chr10: 95,545,475-95,546,464 , GRCh38.p12 chr10: 93,785,718-93,786,707 LGI1, LOC105378437
    nsv4734763copy number variation1nstd199human GRCh37 chr10: 95,526,316-95,526,454 , GRCh38.p12 chr10: 93,766,559-93,766,697 LGI1, LOC105378437
    nsv4682030copy number variation2nstd102humanPathogenic GRCh37 chr10: 94,921,066-95,557,580 , GRCh38.p12 chr10: 93,161,309-93,797,823 LGI1, LOC105378437, 11 more genes
    nsv4672208copy number variation1nstd186human GRCh37 chr10: 95,545,724-95,545,903 , GRCh38.p12 chr10: 93,785,967-93,786,146 LGI1, LOC105378437
    nsv4653883copy number variation3nstd186human GRCh37 chr10: 95,545,477-95,546,495 , GRCh38.p12 chr10: 93,785,720-93,786,738 LGI1, LOC105378437
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