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Items: 1 to 20 of 199

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073286inversion1nstd229human GRCh38 chr16: 84,799,664-85,287,657 , GRCh37.p13 chr16: 84,833,270-85,321,263 LOC123862, MIR12128, 13 more genes
    nsv6997566copy number variation1nstd229human GRCh38 chr16: 85,284,415-85,328,860 , GRCh37.p13 chr16: 85,318,021-85,362,466 LINC00311, GSE1, 3 more genes
    nsv6997223copy number variation1nstd229human GRCh38 chr16: 85,285,519-85,285,770 , GRCh37.p13 chr16: 85,319,125-85,319,376 GSE1, LINC00311
    nsv6993674copy number variation1nstd229human GRCh38 chr16: 85,149,101-85,291,800 , GRCh37.p13 chr16: 85,182,707-85,325,406 GSE1, LINC02139, 4 more genes
    nsv6990775copy number variation1nstd229human GRCh38 chr16: 85,281,229-85,284,445 , GRCh37.p13 chr16: 85,314,835-85,318,051 GSE1, LINC00311
    nsv6988348copy number variation1nstd229human GRCh38 chr16: 85,279,359-85,287,967 , GRCh37.p13 chr16: 85,312,965-85,321,573 LINC00311, GSE1, 1 more genes
    nsv6988186copy number variation1nstd229human GRCh38 chr16: 84,765,972-85,486,232 , GRCh37.p13 chr16: 84,799,578-85,519,838 KIAA0513, MIR5093, 17 more genes
    nsv6985778copy number variation1nstd229human GRCh38 chr16: 84,931,263-85,452,308 , GRCh37.p13 chr16: 84,964,869-85,485,914 KIAA0513, MIR12128, 12 more genes
    nsv6984346copy number variation1nstd229human GRCh38 chr16: 84,940,101-85,330,600 , GRCh37.p13 chr16: 84,973,707-85,364,206 LOC101928502, LOC107984830, 12 more genes
    nsv6984163copy number variation1nstd229human GRCh38 chr16: 85,142,364-85,459,522 , GRCh37.p13 chr16: 85,175,970-85,493,128 GSE1, MIR5093, 7 more genes
    nsv6982259copy number variation1nstd229human GRCh38 chr16: 85,286,174-85,332,922 , GRCh37.p13 chr16: 85,319,780-85,366,528 LOC107984830, LOC101928502, 3 more genes
    nsv6980319copy number variation1nstd229human GRCh38 chr16: 84,592,847-85,544,248 , GRCh37.p13 chr16: 84,626,453-85,577,854 COX6CP16, LINC02176, 20 more genes
    nsv6978784copy number variation1nstd229human GRCh38 chr16: 85,260,869-85,311,275 , GRCh37.p13 chr16: 85,294,475-85,344,881 LINC00311, MIR5093, 4 more genes
    nsv6978407copy number variation1nstd229human GRCh38 chr16: 85,169,601-85,611,300 , GRCh37.p13 chr16: 85,203,207-85,644,906 GSE1, LINC00311, 5 more genes
    nsv6634465copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 71,610,276-90,354,753 , GRCh38.p12 chr16: 71,576,373-90,228,345 AP1G1, AFG3L1P, 349 more genes
    nsv6623996copy number variation1nstd224human GRCh37 chr16: 85,201,970-85,462,981 , GRCh38.p12 chr16: 85,168,364-85,429,375 GSE1, LINC00311, 6 more genes
    nsv6590742inversion1nstd223human GRCh38 chr16: 83,952,013-85,834,110 , GRCh37.p13 chr16: 83,985,618-85,867,716 LOC101928502, LOC105371382, 47 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6314016copy number variation1nstd102humanUncertain significance GRCh37 chr16: 84,134,463-85,705,611 , GRCh38.p12 chr16: 84,100,858-85,672,005 DNAAF1, COTL1, 34 more genes
    nsv6290331copy number variation1nstd102humanPathogenic GRCh37 chr16: 80,386,595-90,163,348 , GRCh38.p12 chr16: 80,352,698-90,096,940 GINS2, TCF25, 220 more genes
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