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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5728039mobile element insertion1nstd211human GRCh38 chr13: 46,249,845-46,249,845 , GRCh37.p13 chr13: 46,823,980-46,823,980 RN7SKP5, LRRC63
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5561330sequence alteration1nstd206human GRCh38 chr13: 44,983,377-49,709,767 , GRCh37.p13 chr13: 45,557,512-50,283,903 , ESD, 103 more genes
    nsv5559366mobile element insertion1nstd206human GRCh38 chr13: 46,249,861-46,249,896 , GRCh37.p13 chr13: 46,823,996-46,824,031 LRRC63, RN7SKP5
    nsv5513317copy number variation1nstd206human GRCh38 chr13: 46,232,316-46,407,940 , GRCh37.p13 chr13: 46,806,451-46,982,075 RUBCNL, LRRC63, 5 more genes
    nsv5495655copy number variation1nstd206human GRCh38 chr13: 46,052,372-46,294,537 , GRCh37.p13 chr13: 46,626,507-46,868,672 LCP1, LOC107984578, 10 more genes
    nsv5196411mobile element insertion1nstd203human GRCh38 chr13: 46,250,366-46,250,384 , GRCh37.p13 chr13: 46,824,501-46,824,519 RN7SKP5, LRRC63
    nsv5150124mobile element insertion1nstd203human GRCh38 chr13: 46,250,622-46,250,635 , GRCh37.p13 chr13: 46,824,757-46,824,770 RN7SKP5, LRRC63
    nsv4997204copy number variation1nstd200human GRCh38 chr13: 43,050,454-56,920,222 , GRCh37.p13 chr13: 43,624,590-57,494,356 , RNY3P2, 222 more genes
    nsv4728809copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 45,487,628-52,639,336 , GRCh38.p12 chr13: 44,913,493-52,065,200 ATP7B, RCBTB2, 155 more genes
    nsv4679126copy number variation1nstd189human GRCh37.p13 chr13: 44,655,843-47,186,905 , GRCh38.p12 chr13: 44,081,707-46,612,770 , CPB2, 69 more genes
    nsv4607802copy number variation1nstd183human GRCh37 chr13: 46,707,942-46,828,580 , GRCh38.p12 chr13: 46,133,807-46,254,445 LCP1, LRRC63, 4 more genes
    nsv4381419copy number variation1nstd173human GRCh37 chr13: 46,589,256-51,939,619 , GRCh38.p12 chr13: 46,015,121-51,365,483 , RNU6-68P, 105 more genes
    nsv4225806copy number variation1nstd166human GRCh37.p13 chr13: 46,806,451-46,982,075 , GRCh38.p12 chr13: 46,232,316-46,407,940 RUBCNL, LRRC63, 5 more genes
    nsv3958789copy number variation1nstd168human GRCh38 chr13: 46,218,312-46,339,105 , GRCh37.p13 chr13: 46,792,447-46,913,240 LINC00563, RN7SKP5, 3 more genes
    nsv3924676copy number variation1nstd102humanPathogenic GRCh38 chr13: 18,456,040-114,340,285 , GRCh37 chr13: 19,030,180-115,105,760 , NCBI36 chr13: 17,928,180-114,123,862 GRTP1, FABP5P1, 1334 more genes
    nsv3924528copy number variation1nstd102humanPathogenic GRCh37 chr13: 41,516,434-115,085,141 , GRCh38 chr13: 40,942,298-114,340,331 , NCBI36 chr13: 40,414,434-114,123,908 LOC105370271, OR7E33P, 925 more genes
    nsv3924173copy number variation1nstd102humanPathogenic GRCh38 chr13: 43,505,396-49,983,668 , NCBI36 chr13: 42,977,532-49,455,805 , GRCh37 chr13: 44,079,532-50,557,804 PCNPP5, LOC105370198, 131 more genes
    nsv3924052copy number variation1nstd102humanPathogenic GRCh38 chr13: 41,288,493-85,137,552 , NCBI36 chr13: 40,760,629-84,609,688 , GRCh37 chr13: 41,862,629-85,711,687 TMEM272, LOC105370241, 535 more genes
    nsv3923911copy number variation1nstd102humanPathogenic GRCh37 chr13: 38,438,363-68,537,920 , GRCh38 chr13: 37,864,226-67,963,788 , NCBI36 chr13: 37,336,363-67,435,921 MLNR, SIAH3, 422 more genes
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