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Items: 1 to 20 of 89

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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
    nsv6915019copy number variation1nstd229human GRCh38 chr11: 62,971,029-62,983,927 , GRCh37.p13 chr11: 62,738,501-62,751,399 SLC22A6
    nsv6910053copy number variation1nstd229human GRCh38 chr11: 62,363,901-63,050,100 , GRCh37.p13 chr11: 62,131,373-62,817,572 MIR6747, TMEM179B, 54 more genes
    nsv6908114copy number variation1nstd229human GRCh38 chr11: 62,593,901-63,028,400 , GRCh37.p13 chr11: 62,361,373-62,795,872 GANAB, SLC22A6, 44 more genes
    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
    nsv6904565copy number variation1nstd229human GRCh38 chr11: 62,240,001-63,046,600 , GRCh37.p13 chr11: 62,007,473-62,814,072 RCC2P6, SNORD26, 58 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
    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
    nsv6313923copy number variation1nstd102humanUncertain significance GRCh37 chr11: 62,670,903-62,820,292 , GRCh38.p12 chr11: 62,903,431-63,052,820 SLC22A6, TUBAP7, 5 more genes
    nsv5494569copy number variation1nstd206human GRCh38 chr11: 62,950,117-63,024,043 , GRCh37.p13 chr11: 62,717,589-62,791,515 SLC22A6, SLC22A8, 1 more genes
    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
    nsv5311945copy number variation1nstd204human GRCh38.p13 chr11: 62,978,454-62,983,416 , GRCh37.p13 chr11: 62,745,926-62,750,888 SLC22A6
    nsv5277402copy number variation1nstd204human GRCh38.p13 chr11: 62,978,748-62,982,763 , GRCh37.p13 chr11: 62,746,220-62,750,235 SLC22A6
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
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