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Items: 1 to 20 of 105

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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
    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
    nsv6911663copy number variation1nstd229human GRCh38 chr11: 63,553,081-63,574,224 , GRCh37.p13 chr11: 63,320,553-63,341,696 PLAAT3, LOC105369335, 1 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
    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
    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
    nsv6461751copy number variation1nstd223human GRCh38 chr11: 63,565,201-63,568,600 , GRCh37.p13 chr11: 63,332,673-63,336,072 PLAAT2
    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
    nsv6132371copy number variation1nstd213human GRCh37 chr11: 63,120,000-64,210,001 , GRCh38.p12 chr11: 63,352,528-64,442,529 VEGFB, FLRT1, 51 more genes
    nsv6132183copy number variation1nstd213human GRCh37 chr11: 63,160,000-63,380,001 , GRCh38.p12 chr11: 63,392,528-63,612,529 PLAAT4, TMSB4XP5, 7 more genes
    nsv6090055insertion1nstd212human GRCh38 chr11: 63,559,614-63,559,614 , GRCh37.p13 chr11: 63,327,086-63,327,086 PLAAT2
    nsv5974531insertion1nstd209human GRCh38 chr11: 63,559,614-63,559,614 , GRCh37.p13 chr11: 63,327,086-63,327,086 PLAAT2
    nsv5654405insertion1nstd207human GRCh38 chr11: 63,559,614-63,559,614 , GRCh37.p13 chr11: 63,327,086-63,327,086 PLAAT2
    nsv5543760insertion1nstd206human GRCh38 chr11: 63,559,614-63,559,614 , GRCh37.p13 chr11: 63,327,086-63,327,086 PLAAT2
    nsv5510354copy number variation1nstd206human GRCh38 chr11: 63,549,737-63,585,264 , GRCh37.p13 chr11: 63,317,209-63,352,736 PLAAT2, PLAAT3, 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
    nsv4834153copy number variation1nstd200human GRCh37 chr11: 63,333,021-63,336,174 , GRCh38.p12 chr11: 63,565,549-63,568,702 PLAAT2
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