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Items: 1 to 20 of 92

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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
    nsv6907980copy number variation1nstd229human GRCh38 chr11: 63,053,606-63,128,550 , GRCh37.p13 chr11: 62,821,078-62,896,022 RPL29P22, SLC22A24
    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
    nsv6637428copy number variation1nstd102humanUncertain significance GRCh37 chr11: 62,838,127-63,118,199 , GRCh38.p12 chr11: 63,070,655-63,350,727 SLC22A25, SLC22A10, 4 more genes
    nsv6621125copy number variation1nstd224human GRCh37 chr11: 62,847,161-63,079,161 , GRCh38.p12 chr11: 63,079,689-63,311,689 CCND2P1, SLC22A24, 4 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6291276copy number variation1nstd102humanUncertain significance GRCh37 chr11: 62,782,711-63,122,730 , GRCh38.p12 chr11: 63,015,239-63,355,258 TUBAP7, RPL29P22, 7 more genes
    nsv6132064inversion1nstd213human GRCh37 chr11: 62,834,728-63,072,311 , GRCh38.p12 chr11: 63,067,256-63,304,839 CCND2P1, SLC22A24, 4 more genes
    nsv6131829inversion1nstd213human GRCh37 chr11: 62,834,704-63,072,307 , GRCh38.p12 chr11: 63,067,232-63,304,835 CCND2P1, SLC22A24, 4 more genes
    nsv5925763copy number variation1nstd209human GRCh38 chr11: 63,106,903-63,127,938 , GRCh37.p13 chr11: 62,874,375-62,895,410 RPL29P22, SLC22A24
    nsv5851121copy number variation1nstd209human GRCh38 chr11: 63,107,113-63,127,984 , GRCh37.p13 chr11: 62,874,585-62,895,456 RPL29P22, SLC22A24
    nsv5513077copy number variation1nstd206human GRCh38 chr11: 63,106,937-63,127,977 , GRCh37.p13 chr11: 62,874,409-62,895,449 RPL29P22, SLC22A24
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
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