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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5656104insertion1nstd207human GRCh38 chr13: 51,348,694-51,348,694 , GRCh37.p13 chr13: 51,922,830-51,922,830 SERPINE3, MIR5693
    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
    nsv5513011copy number variation1nstd206human GRCh38 chr13: 51,348,686-51,348,848 , GRCh37.p13 chr13: 51,922,822-51,922,984 MIR5693, SERPINE3
    nsv5511517copy number variation1nstd206human GRCh38 chr13: 51,345,804-51,346,771 , GRCh37.p13 chr13: 51,919,940-51,920,907 SERPINE3, MIR5693
    nsv5390353copy number variation2nstd186human GRCh37 chr13: 51,922,822-51,922,984 , GRCh38.p12 chr13: 51,348,686-51,348,848 MIR5693, SERPINE3
    nsv5389798copy number variation1nstd186human GRCh37 chr13: 51,922,822-51,922,983 , GRCh38.p12 chr13: 51,348,686-51,348,847 MIR5693, SERPINE3
    nsv5303989copy number variation1nstd204human GRCh38.p13 chr13: 51,348,686-51,348,847 , GRCh37.p13 chr13: 51,922,822-51,922,983 MIR5693, SERPINE3
    nsv5004597copy number variation1nstd200human GRCh38 chr13: 51,348,686-51,348,847 , GRCh37.p13 chr13: 51,922,822-51,922,983 MIR5693, SERPINE3
    nsv4997204copy number variation1nstd200human GRCh38 chr13: 43,050,454-56,920,222 , GRCh37.p13 chr13: 43,624,590-57,494,356 , RNY3P2, 222 more genes
    nsv4841264copy number variation1nstd200human GRCh37 chr13: 51,922,822-51,922,984 , GRCh38.p12 chr13: 51,348,686-51,348,848 SERPINE3, MIR5693
    nsv4752712insertion1nstd199human GRCh37 chr13: 51,922,901-51,922,901 , GRCh38.p12 chr13: 51,348,765-51,348,765 SERPINE3, MIR5693
    nsv4738802copy number variation1nstd199human GRCh38.p12 chr13: 51,348,765-51,348,933 , GRCh37 chr13: 51,922,901-51,923,069 SERPINE3, MIR5693
    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
    nsv4675995copy number variation1nstd102humanPathogenic GRCh37 chr13: 51,512,603-91,631,111 , GRCh38.p12 chr13: 50,938,467-90,978,857 RNU7-88P, LINC00564, 396 more genes
    nsv4456820copy number variation1nstd102humanUncertain significance GRCh37 chr13: 49,586,017-61,311,845 , GRCh38.p12 chr13: 49,011,881-60,737,711 MIR759, CAB39L, 149 more genes
    nsv4444856insertion1nstd175human GRCh37 chr13: 51,922,815-51,922,815 , GRCh38.p12 chr13: 51,348,679-51,348,679 SERPINE3, MIR5693
    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
    nsv3942045insertion1nstd167human GRCh37 chr13: 51,922,830-51,922,830 , GRCh38.p12 chr13: 51,348,694-51,348,694 SERPINE3, MIR5693
    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
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