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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7064398inversion1nstd229human GRCh38 chr11: 62,881,040-63,382,431 , GRCh37.p13 chr11: 62,648,512-63,149,903 SLC3A2, SLC22A25, 13 more genes
    nsv7061431inversion1nstd229human GRCh38 chr11: 62,880,871-63,484,120 , GRCh37.p13 chr11: 62,648,343-63,251,592 LOC105369333, CHRM1, 15 more genes
    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
    nsv6915722copy number variation1nstd229human GRCh38 chr11: 63,383,049-63,400,151 , GRCh37.p13 chr11: 63,150,521-63,167,623 SLC22A9
    nsv6913624copy number variation1nstd229human GRCh38 chr11: 63,377,123-63,377,158 , GRCh37.p13 chr11: 63,144,595-63,144,630 SLC22A9
    nsv6909933copy number variation1nstd229human GRCh38 chr11: 63,376,801-63,381,000 , GRCh37.p13 chr11: 63,144,273-63,148,472 SLC22A9
    nsv6907002copy number variation1nstd229human GRCh38 chr11: 63,367,618-63,375,946 , GRCh37.p13 chr11: 63,135,090-63,143,418 SLC22A9
    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
    nsv6903860copy number variation1nstd229human GRCh38 chr11: 63,382,153-63,386,693 , GRCh37.p13 chr11: 63,149,625-63,154,165 SLC22A9
    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
    nsv6901347copy number variation1nstd229human GRCh38 chr11: 63,404,784-63,408,896 , GRCh37.p13 chr11: 63,172,256-63,176,368 SLC22A9
    nsv6621194copy number variation1nstd224human GRCh37 chr11: 63,064,887-63,350,253 , GRCh38.p12 chr11: 63,297,415-63,582,781 PLAAT2, SLC22A10, 8 more genes
    nsv6472996copy number variation1nstd223human GRCh38 chr11: 63,381,787-63,382,473 , GRCh37.p13 chr11: 63,149,259-63,149,945 SLC22A9
    nsv6468929copy number variation1nstd223human GRCh38 chr11: 63,370,321-63,370,941 , GRCh37.p13 chr11: 63,137,793-63,138,413 SLC22A9
    nsv6466796copy number variation1nstd223human GRCh38 chr11: 63,338,270-63,367,739 , GRCh37.p13 chr11: 63,105,742-63,135,211 SLC22A9
    nsv6466554copy number variation1nstd223human GRCh38 chr11: 63,399,201-63,401,400 , GRCh37.p13 chr11: 63,166,673-63,168,872 SLC22A9
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