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Items: 1 to 20 of 82

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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
    nsv7032755copy number variation1nstd229human GRCh38 chr20: 60,346,437-61,454,169 , GRCh37.p13 chr20: 58,921,495-60,029,225 LOC105372703, LOC101928048, 8 more genes
    nsv7029906copy number variation1nstd229human GRCh38 chr20: 60,439,901-60,753,000 , GRCh37.p13 chr20: 59,014,959-59,328,057 LOC101928048, MIR4533, 2 more genes
    nsv7029638copy number variation1nstd229human GRCh38 chr20: 60,472,415-60,474,669 , GRCh37.p13 chr20: 59,047,473-59,049,727 LOC101928048
    nsv7023628copy number variation1nstd229human GRCh38 chr20: 60,417,127-60,491,421 , GRCh37.p13 chr20: 58,992,185-59,066,479 MIR4533, LOC101928048
    nsv7022296copy number variation1nstd229human GRCh38 chr20: 60,432,906-60,571,665 , GRCh37.p13 chr20: 59,007,964-59,146,723 MIR4533, MIR548AG2, 1 more genes
    nsv7021100copy number variation1nstd229human GRCh38 chr20: 59,995,939-60,524,337 , GRCh37.p13 chr20: 58,570,994-59,099,395 LINC02910, MIR4533, 8 more genes
    nsv6626799copy number variation1nstd224human GRCh37 chr20: 58,993,857-59,061,433 , GRCh38.p12 chr20: 60,418,799-60,486,375 MIR4533, LOC101928048
    nsv6596718inversion1nstd223human GRCh38 chr20: 60,471,386-60,471,819 , GRCh37.p13 chr20: 59,046,444-59,046,877 LOC101928048
    nsv6314208copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,835,739-62,915,555 , GRCh38.p12 chr20: 58,260,683-64,284,202 LOC105372698, LOC105372695, 176 more genes
    nsv6134310copy number variation1nstd213human GRCh37 chr20: 58,900,000-59,290,001 , GRCh38.p12 chr20: 60,324,942-60,714,943 MTCO2P1, MIR4533, 3 more genes
    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
    nsv6134177copy number variation1nstd213human GRCh37 chr20: 59,030,000-59,400,001 , GRCh38.p12 chr20: 60,454,942-60,824,945 MIR4533, MIR548AG2, 3 more genes
    nsv6134045copy number variation1nstd213human GRCh37 chr20: 58,760,000-60,230,001 , GRCh38.p12 chr20: 60,184,942-61,654,945 LINC01718, LOC105372698, 12 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
    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
    nsv5025774copy number variation1nstd200human GRCh38 chr20: 60,469,411-60,473,223 , GRCh37.p13 chr20: 59,044,469-59,048,281 LOC101928048
    nsv5025771copy number variation1nstd200human GRCh38 chr20: 60,155,509-60,990,304 , GRCh37.p13 chr20: 58,730,565-59,565,360 MIR646, MIR4533, 8 more genes
    nsv4865679copy number variation1nstd200human GRCh37 chr20: 58,730,565-59,565,360 , GRCh38.p12 chr20: 60,155,509-60,990,304 LOC105372698, MIR4533, 8 more genes
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