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Items: 1 to 20 of 111

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6911667copy number variation1nstd229human GRCh38 chr11: 57,370,301-57,382,600 , GRCh37.p13 chr11: 57,137,774-57,150,073 PRG3, P2RX3
    nsv6637373copy number variation1nstd102humanUncertain significance GRCh37 chr11: 56,637,024-57,361,915 , GRCh38.p12 chr11: 56,869,548-57,594,442 OR5BQ1P, OR5AK2, 27 more genes
    nsv6467396copy number variation1nstd223human GRCh38 chr11: 57,373,446-57,383,321 , GRCh37.p13 chr11: 57,140,919-57,150,794 PRG3
    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
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 TRR-TCT3-2, OR4A41P, 494 more genes
    nsv6291401copy number variation1nstd102humannot provided GRCh37 chr11: 57,112,299-57,871,866 , GRCh38.p12 chr11: 57,344,825-58,104,394 RN7SL605P, CLP1, 35 more genes
    nsv6291003copy number variation1nstd102humanUncertain significance GRCh37 chr11: 57,037,091-57,453,575 , GRCh38.p12 chr11: 57,269,617-57,686,103 PRG2, SLC43A1, 19 more genes
    nsv6101017inversion1nstd212human GRCh38 chr11: 54,578,670-59,501,927 , GRCh37.p13 chr11: 54,711,406-59,269,400 , APLNR, 236 more genes
    nsv6086008insertion1nstd212human GRCh38 chr11: 57,376,525-57,376,525 , GRCh37.p13 chr11: 57,143,998-57,143,998 PRG3
    nsv6023566copy number variation1nstd212human GRCh38 chr11: 57,376,100-57,376,507 , GRCh37.p13 chr11: 57,143,573-57,143,980 PRG3
    nsv5914325copy number variation1nstd209human GRCh38 chr11: 55,273,256-58,053,631 , GRCh37.p13 chr11: 55,040,732-57,821,103 , LOC107984365, 161 more genes
    nsv5650127insertion1nstd207human GRCh38 chr11: 57,376,525-57,376,525 , GRCh37.p13 chr11: 57,143,998-57,143,998 PRG3
    nsv5501031copy number variation1nstd206human GRCh38 chr11: 57,376,680-57,380,318 , GRCh37.p13 chr11: 57,144,153-57,147,791 PRG3
    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
    nsv5272801copy number variation1nstd204human GRCh38.p13 chr11: 57,375,701-57,376,500 , GRCh37.p13 chr11: 57,143,174-57,143,973 PRG3
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4711974copy number variation1nstd195human GRCh37 chr11: 57,143,650-57,143,651 , GRCh38.p12 chr11: 57,376,177-57,376,178 PRG3
    nsv4680588copy number variation1nstd189human GRCh37.p13 chr11: 55,444,212-57,222,540 , GRCh38.p12 chr11: 55,676,736-57,455,067 , APLNR, 109 more genes
    nsv4615605copy number variation1nstd183human GRCh37 chr11: 57,143,327-57,146,038 , GRCh38.p12 chr11: 57,375,854-57,378,565 PRG3
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