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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 WAPL, RNU7-12P, 1876 more genes
    nsv3920295copy number variation1nstd102humanPathogenic NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422 WAPL, EIF2S2P3, 895 more genes
    nsv6637542copy number variation1nstd102humanPathogenic GRCh37 chr10: 82,595,472-93,542,416 , GRCh38.p12 chr10: 80,835,716-91,782,659 WAPL, IFIT6P, 166 more genes
    nsv3891568copy number variation1nstd102humanPathogenic GRCh37 chr10: 83,379,241-93,219,169 , GRCh38.p12 chr10: 81,619,485-91,459,412 WAPL, NAPGP1, 157 more genes
    nsv6634458copy number variation1nstd102humanPathogenic GRCh37 chr10: 83,533,660-91,913,077 , GRCh38.p12 chr10: 81,773,904-90,153,320 WAPL, IFIT5, 140 more genes
    nsv4729484copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,457,752-89,253,430 , GRCh38.p12 chr10: 79,697,996-87,493,673 WAPL, DPY19L2P5, 115 more genes
    nsv3923084copy number variation1nstd102humanPathogenic NCBI36 chr10: 81,149,191-89,108,131 , GRCh38 chr10: 79,719,429-87,358,394 , GRCh37 chr10: 81,479,185-89,118,151 WAPL, LINC02650, 110 more genes
    nsv3910996copy number variation1nstd102humanPathogenic NCBI36 chr10: 81,541,288-89,108,131 , GRCh38 chr10: 79,802,022-87,358,394 , GRCh37 chr10: 81,561,459-89,118,151 WAPL, HMGN2P8, 110 more genes
    nsv3910032copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,449,116-88,983,530 , NCBI36 chr10: 81,119,122-88,973,510 , GRCh38 chr10: 79,689,360-87,223,773 WAPL, LINC02655, 109 more genes
    nsv4729317copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,617,260-89,146,780 , GRCh38.p12 chr10: 79,857,504-87,387,023 WAPL, LOC105378390, 109 more genes
    nsv4728260copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,585,301-89,101,700 , GRCh38.p12 chr10: 79,825,545-87,341,943 WAPL, C1DP3, 109 more genes
    nsv3910650copy number variation1nstd102humanPathogenic NCBI36 chr10: 81,648,252-89,108,131 , GRCh38 chr10: 79,898,516-87,358,394 , GRCh37 chr10: 81,658,272-89,118,151 WAPL, ZNRF2P3, 103 more genes
    nsv3891947copy number variation2nstd102humanPathogenic GRCh37 chr10: 81,617,260-88,980,961 , GRCh38.p12 chr10: 79,857,504-87,221,204 WAPL, RNU1-65P, 104 more genes
    nsv3897099copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,597,767-88,951,347 , GRCh38.p12 chr10: 79,838,011-87,191,590 WAPL, NRG3, 104 more genes
    nsv6315478copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,630,468-88,980,961 , GRCh38.p12 chr10: 79,870,712-87,221,204 WAPL, RNU1-19P, 102 more genes
    nsv3911129copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,640,994-88,940,429 , GRCh38 chr10: 79,881,238-87,180,672 , NCBI36 chr10: 81,630,974-88,930,409 WAPL, LOC100130698, 99 more genes
    nsv3922892copy number variation1nstd102humanPathogenic GRCh38 chr10: 79,802,022-87,068,261 , GRCh37 chr10: 81,561,459-88,828,018 , NCBI36 chr10: 81,263,385-88,817,998 WAPL, LINC02655, 103 more genes
    nsv3922465copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,658,272-88,869,584 , GRCh38 chr10: 79,898,516-87,109,827 , NCBI36 chr10: 81,648,252-88,859,564 WAPL, FARSBP1, 97 more genes
    nsv3918925copy number variation1nstd102humanPathogenic NCBI36 chr10: 81,631,898-88,817,998 , GRCh38 chr10: 79,882,162-87,068,261 , GRCh37 chr10: 81,641,918-88,828,018 WAPL, LOC105378387, 97 more genes
    nsv3891414copy number variation1nstd102humanPathogenic GRCh37 chr10: 82,013,260-89,166,455 , GRCh38.p12 chr10: 80,253,504-87,406,698 WAPL, LOC105378392, 90 more genes
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