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Items: 1 to 20 of 176

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7060123inversion1nstd229human GRCh38 chr20: 24,968,979-24,968,996 , GRCh37.p13 chr20: 24,949,615-24,949,632 APMAP
    nsv7058531inversion1nstd229human GRCh38 chr20: 24,972,530-24,973,879 , GRCh37.p13 chr20: 24,953,166-24,954,515 APMAP, RNU6-1257P
    nsv7037094copy number variation1nstd229human GRCh38 chr20: 23,996,469-25,641,348 , GRCh37.p13 chr20: 23,977,106-25,621,984 CST7, LOC105372579, 28 more genes
    nsv7035258copy number variation1nstd229human GRCh38 chr20: 24,250,776-25,542,572 , GRCh37.p13 chr20: 24,231,412-25,523,208 LOC105372581, LINC02967, 21 more genes
    nsv7032689copy number variation1nstd229human GRCh38 chr20: 24,734,950-25,022,314 , GRCh37.p13 chr20: 24,715,586-25,002,950 APMAP, LINC02967, 4 more genes
    nsv7032398copy number variation1nstd229human GRCh38 chr20: 24,956,949-24,981,638 , GRCh37.p13 chr20: 24,937,585-24,962,274 CST7, RNU6-1257P, 1 more genes
    nsv7023272copy number variation1nstd229human GRCh38 chr20: 24,979,052-24,998,311 , GRCh37.p13 chr20: 24,959,688-24,978,947 APMAP
    nsv7020766copy number variation1nstd229human GRCh38 chr20: 24,993,347-24,993,388 , GRCh37.p13 chr20: 24,973,983-24,974,024 APMAP
    nsv6626758copy number variation1nstd224human GRCh37 chr20: 24,504,850-26,252,906 , GRCh38.p12 chr20: 24,524,214-26,272,270 NINL, PPIAP2, 39 more genes
    nsv6626335copy number variation1nstd224human GRCh37 chr20: 24,708,653-25,539,486 , GRCh38.p12 chr20: 24,728,017-25,558,850 ENTPD6, NINL, 17 more genes
    nsv6525735copy number variation1nstd223human GRCh38 chr20: 24,961,955-24,962,134 , GRCh37.p13 chr20: 24,942,591-24,942,770 APMAP
    nsv6520886copy number variation1nstd223human GRCh38 chr20: 24,835,426-25,188,640 , GRCh37.p13 chr20: 24,816,062-25,169,276 CST7, LOC284798, 8 more genes
    nsv6518445copy number variation1nstd223human GRCh38 chr20: 24,978,972-24,979,104 , GRCh37.p13 chr20: 24,959,608-24,959,740 APMAP
    nsv6291578copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 18,665,879-33,903,216 , GRCh38.p12 chr20: 18,685,235-35,315,413 AHCY, ASIP, 330 more genes
    nsv6277408copy number variation1nstd214human GRCh38 chr20: 24,962,262-24,962,381 , GRCh37.p13 chr20: 24,942,898-24,943,017 APMAP
    nsv6251340mobile element insertion1nstd215human GRCh38 chr20: 24,974,876-24,974,876 , GRCh37.p13 chr20: 24,955,512-24,955,512 APMAP
    nsv6224715copy number variation1nstd214human GRCh38 chr20: 24,961,582-24,961,641 , GRCh37.p13 chr20: 24,942,218-24,942,277 APMAP
    nsv6214138copy number variation1nstd214human GRCh38 chr20: 24,972,066-24,972,147 , GRCh37.p13 chr20: 24,952,702-24,952,783 APMAP
    nsv6212273copy number variation1nstd214human GRCh38 chr20: 24,982,234-24,982,290 , GRCh37.p13 chr20: 24,962,870-24,962,926 APMAP
    nsv6134018copy number variation1nstd213human GRCh37 chr20: 23,950,000-25,300,001 , GRCh38.p12 chr20: 23,969,363-25,319,365 ENTPD6, PYGB, 23 more genes
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