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Items: 1 to 20 of 344

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071638inversion1nstd229human GRCh38 chr13: 55,583,879-63,209,085 , GRCh37.p13 chr13: 56,158,014-63,783,218 MIR3169, PCDH20, 66 more genes
    nsv7067987inversion1nstd229human GRCh38 chr13: 59,595,201-60,245,086 , GRCh37.p13 chr13: 60,169,335-60,819,220 DIAPH3-AS2, LOC105370227, 5 more genes
    nsv6957798copy number variation1nstd229human GRCh38 chr13: 60,220,058-60,220,106 , GRCh37.p13 chr13: 60,794,192-60,794,240 LINC00434
    nsv6955320copy number variation1nstd229human GRCh38 chr13: 60,139,401-60,348,800 , GRCh37.p13 chr13: 60,713,535-60,922,934 LOC105370228, RNY4P28, 5 more genes
    nsv6954647copy number variation1nstd229human GRCh38 chr13: 59,914,801-60,316,300 , GRCh37.p13 chr13: 60,488,935-60,890,434 LOC105370227, DIAPH3-AS2, 6 more genes
    nsv6952934copy number variation1nstd229human GRCh38 chr13: 60,219,106-60,219,123 , GRCh37.p13 chr13: 60,793,240-60,793,257 LINC00434
    nsv6952328copy number variation1nstd229human GRCh38 chr13: 60,211,308-60,253,316 , GRCh37.p13 chr13: 60,785,442-60,827,450 LINC00434
    nsv6951815copy number variation1nstd229human GRCh38 chr13: 60,239,812-60,252,711 , GRCh37.p13 chr13: 60,813,946-60,826,845 LINC00434
    nsv6948105copy number variation1nstd229human GRCh38 chr13: 60,181,301-60,227,200 , GRCh37.p13 chr13: 60,755,435-60,801,334 LINC00434, RNY4P28
    nsv6947793copy number variation1nstd229human GRCh38 chr13: 60,198,829-60,224,979 , GRCh37.p13 chr13: 60,772,963-60,799,113 LINC00434
    nsv6945186copy number variation1nstd229human GRCh38 chr13: 60,208,654-60,216,993 , GRCh37.p13 chr13: 60,782,788-60,791,127 LINC00434
    nsv6945095copy number variation1nstd229human GRCh38 chr13: 60,232,841-60,233,068 , GRCh37.p13 chr13: 60,806,975-60,807,202 LINC00434
    nsv6944025copy number variation1nstd229human GRCh38 chr13: 60,244,001-60,260,800 , GRCh37.p13 chr13: 60,818,135-60,834,934 LINC00434
    nsv6941794copy number variation1nstd229human GRCh38 chr13: 60,264,292-60,264,318 , GRCh37.p13 chr13: 60,838,426-60,838,452 LINC00434
    nsv6938284copy number variation1nstd229human GRCh38 chr13: 59,992,801-60,410,900 , GRCh37.p13 chr13: 60,566,935-60,985,034 DIAPH3, LOC105370227, 8 more genes
    nsv6637880copy number variation1nstd102humanUncertain significance GRCh37 chr13: 56,897,737-64,074,025 , GRCh38.p12 chr13: 56,323,603-63,499,892 DIAPH3-AS2, LOC107984625, 64 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6491047copy number variation1nstd223human GRCh38 chr13: 60,242,701-60,245,800 , GRCh37.p13 chr13: 60,816,835-60,819,934 LINC00434
    nsv6487937copy number variation1nstd223human GRCh38 chr13: 60,239,852-60,240,312 , GRCh37.p13 chr13: 60,813,986-60,814,446 LINC00434
    nsv6483363copy number variation1nstd223human GRCh38 chr13: 60,181,318-60,227,223 , GRCh37.p13 chr13: 60,755,452-60,801,357 LINC00434, RNY4P28
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