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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094175copy number variation1nstd102humanUncertain significance GRCh37 chr11: 63,426,213-63,438,807 , GRCh38.p12 chr11: 63,658,741-63,671,335 ATL3
    nsv7093694copy number variation2nstd102humanUncertain significance GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878 VPS37C, POLR2G, 298 more genes
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv7075313inversion1nstd229human GRCh38 chr11: 62,887,478-63,793,002 , GRCh37.p13 chr11: 62,654,950-63,560,474 RPL29P22, TUBAP7, 25 more genes
    nsv7068274inversion1nstd229human GRCh38 chr11: 63,630,801-63,630,913 , GRCh37.p13 chr11: 63,398,273-63,398,385 ATL3, IMMP1LP1
    nsv7060800inversion1nstd229human GRCh38 chr11: 62,887,439-63,792,997 , GRCh37.p13 chr11: 62,654,911-63,560,469 TUBAP7, ATL3, 25 more genes
    nsv7058098inversion1nstd229human GRCh38 chr11: 62,887,432-63,795,073 , GRCh37.p13 chr11: 62,654,904-63,562,545 TUBAP7, ATL3, 25 more genes
    nsv6917886copy number variation1nstd229human GRCh38 chr11: 63,653,904-63,656,668 , GRCh37.p13 chr11: 63,421,376-63,424,140 ATL3
    nsv6917878copy number variation1nstd229human GRCh38 chr11: 63,659,598-63,679,687 , GRCh37.p13 chr11: 63,427,070-63,447,159 ATL3, RTN3
    nsv6912672copy number variation1nstd229human GRCh38 chr11: 63,648,168-63,654,548 , GRCh37.p13 chr11: 63,415,640-63,422,020 ATL3
    nsv6911884copy number variation1nstd229human GRCh38 chr11: 63,655,895-63,656,912 , GRCh37.p13 chr11: 63,423,367-63,424,384 ATL3
    nsv6908888copy number variation1nstd229human GRCh38 chr11: 63,644,944-63,653,328 , GRCh37.p13 chr11: 63,412,416-63,420,800 ATL3
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 more genes
    nsv6902486copy number variation1nstd229human GRCh38 chr11: 63,650,329-63,664,813 , GRCh37.p13 chr11: 63,417,801-63,432,285 ATL3
    nsv6901389copy number variation1nstd229human GRCh38 chr11: 63,633,537-63,642,594 , GRCh37.p13 chr11: 63,401,009-63,410,066 ATL3
    nsv6898841copy number variation1nstd229human GRCh38 chr11: 63,639,966-63,644,141 , GRCh37.p13 chr11: 63,407,438-63,411,613 ATL3
    nsv6594493inversion1nstd223human GRCh38 chr11: 63,648,846-63,649,432 , GRCh37.p13 chr11: 63,416,318-63,416,904 ATL3
    nsv6586092inversion1nstd223human GRCh38 chr11: 63,661,888-63,662,493 , GRCh37.p13 chr11: 63,429,360-63,429,965 ATL3
    nsv6582421inversion1nstd223human GRCh38 chr11: 63,639,724-63,639,891 , GRCh37.p13 chr11: 63,407,196-63,407,363 ATL3
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