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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057713inversion1nstd229human GRCh38 chr6: 56,332,234-57,502,028 , GRCh37.p13 chr6: 56,197,032-57,366,927 OSTCP6, MIR548U, 16 more genes
    nsv7041912inversion1nstd229human GRCh38 chr6: 57,221,902-57,393,257 , GRCh37.p13 chr6: 57,086,700-57,258,055 LINC03001, PRIM2, 2 more genes
    nsv6790278copy number variation1nstd229human GRCh38 chr6: 57,234,380-57,298,394 , GRCh37.p13 chr6: 57,099,178-57,163,192 LINC03001
    nsv6638066copy number variation1nstd102humanUncertain significance GRCh38 chr6: 53,151,508-58,400,428 , GRCh37.p13 chr6: 53,016,306-58,726,706 NPM1P36, LINC00680-GUSBP4, 73 more genes
    nsv6631070copy number variation1nstd224human GRCh37 chr6: 54,531,949-57,262,543 , GRCh38.p12 chr6: 54,667,151-57,397,745 DST, BAG2, 28 more genes
    nsv6560587inversion1nstd223human GRCh38 chr6: 56,332,312-57,501,978 , GRCh37.p13 chr6: 56,197,110-57,366,877 RCC2P7, COL21A1, 16 more genes
    nsv6410304copy number variation1nstd223human GRCh38 chr6: 57,234,376-57,298,390 , GRCh37.p13 chr6: 57,099,174-57,163,188 LINC03001
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 ACTG1P9, CRISP1, 245 more genes
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5471969copy number variation1nstd206human GRCh38 chr6: 57,237,237-57,328,440 , GRCh37.p13 chr6: 57,102,035-57,193,238 LINC03001, PRIM2
    nsv5464263copy number variation1nstd206human GRCh38 chr6: 57,236,000-57,268,000 , GRCh37.p13 chr6: 57,100,798-57,132,798 LINC03001
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4598661copy number variation1nstd183human GRCh37 chr6: 57,102,054-57,133,174 , GRCh38.p12 chr6: 57,237,256-57,268,376 LINC03001
    nsv4406669copy number variation1nstd174human GRCh37 chr6: 57,102,041-57,162,808 , GRCh38.p12 chr6: 57,237,243-57,298,010 LINC03001
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
    nsv4145434copy number variation1nstd166human GRCh37.p13 chr6: 57,122,148-57,126,768 , GRCh38.p12 chr6: 57,257,350-57,261,970 LINC03001
    nsv4136903copy number variation1nstd166human GRCh37.p13 chr6: 57,101,000-57,133,000 , GRCh38.p12 chr6: 57,236,202-57,268,202 LINC03001
    nsv3922315copy number variation1nstd102humanPathogenic GRCh37 chr6: 50,938,895-57,297,586 , NCBI36 chr6: 51,046,854-57,405,545 , GRCh38 chr6: 50,971,182-57,432,788 MLIP-AS1, GSTA9P, 100 more genes
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