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Items: 1 to 20 of 111

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148186copy number variation1nstd102humanUncertain significance GRCh37 chr20: 52,773,668-62,965,020 , GRCh38.p12 chr20: 54,157,129-64,333,667 LOC105372717, CTCFL, 245 more genes
    nsv7037078copy number variation1nstd229human GRCh38 chr20: 54,988,450-63,850,628 , GRCh37.p13 chr20: 53,604,989-62,481,981 , RPL39P, 209 more genes
    nsv7034033copy number variation1nstd229human GRCh38 chr20: 58,098,800-58,241,875 , GRCh37.p13 chr20: 56,673,856-56,816,931 LOC107985434, HSPD1P19, 5 more genes
    nsv7031526copy number variation1nstd229human GRCh38 chr20: 58,210,577-58,214,561 , GRCh37.p13 chr20: 56,785,633-56,789,617 ANKRD60
    nsv7024807copy number variation1nstd229human GRCh38 chr20: 56,642,648-58,322,378 , GRCh37.p13 chr20: 55,217,704-56,897,434 MIR4325, LOC105372693, 36 more genes
    nsv7024789copy number variation1nstd229human GRCh38 chr20: 58,216,486-58,222,572 , GRCh37.p13 chr20: 56,791,542-56,797,628 ANKRD60
    nsv7018337copy number variation1nstd229human GRCh38 chr20: 57,534,757-58,246,724 , GRCh37.p13 chr20: 56,109,813-56,821,780 CIMIP1, NKILA, 12 more genes
    nsv6547876copy number variation1nstd223human GRCh38 chr20: 58,098,800-58,241,875 , GRCh37.p13 chr20: 56,673,856-56,816,931 CIMIP1, HSPD1P19, 5 more genes
    nsv6547128copy number variation1nstd223human GRCh38 chr20: 58,214,399-58,214,771 , GRCh37.p13 chr20: 56,789,455-56,789,827 ANKRD60
    nsv6541009copy number variation1nstd223human GRCh38 chr20: 58,215,027-58,369,755 , GRCh37.p13 chr20: 56,790,083-56,944,811 ANKRD60, PPP4R1L, 1 more genes
    nsv6314094copy number variation1nstd102humanPathogenic GRCh37 chr20: 55,292,205-57,866,365 , GRCh38.p12 chr20: 56,717,149-59,291,310 PCK1, MIR296, 58 more genes
    nsv6311086copy number variation1nstd102humanUncertain significance GRCh37 chr20: 54,823,900-57,899,514 , GRCh38.p12 chr20: 56,248,844-59,324,459 CTSZ, SPO11, 75 more genes
    nsv6220307copy number variation1nstd214human GRCh38 chr20: 58,219,696-58,219,745 , GRCh37.p13 chr20: 56,794,752-56,794,801 ANKRD60
    nsv6134308copy number variation1nstd213human GRCh37 chr20: 55,660,000-60,880,001 , GRCh38.p12 chr20: 57,084,944-62,304,945 TAF4, OSBPL2, 97 more genes
    nsv6134173copy number variation1nstd213human GRCh37 chr20: 56,380,000-56,840,001 , GRCh38.p12 chr20: 57,804,944-58,264,945 PPP4R1L, CIMIP1, 7 more genes
    nsv6134040copy number variation1nstd213human GRCh37 chr20: 51,820,000-60,870,001 , GRCh38.p12 chr20: 53,203,461-62,294,945 MC3R, PPP1R3D, 142 more genes
    nsv6133831copy number variation1nstd213human GRCh37 chr20: 54,010,000-57,120,001 , GRCh38.p12 chr20: 55,393,462-58,544,945 BMP7, SPO11, 62 more genes
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5025764copy number variation1nstd200human GRCh38 chr20: 58,214,989-58,369,779 , GRCh37.p13 chr20: 56,790,045-56,944,835 RAB22A, ANKRD60, 1 more genes
    nsv4865674copy number variation1nstd200human GRCh37 chr20: 56,790,021-56,944,838 , GRCh38.p12 chr20: 58,214,965-58,369,782 ANKRD60, PPP4R1L, 1 more genes
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