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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5887973copy number variation1nstd209human GRCh38 chr6: 32,812,043-32,885,630 , GRCh37.p13 chr6: 32,779,820-32,853,407 HLA-DOB, PSMB8, 5 more genes
    nsv5300641copy number variation1nstd204human GRCh37.p13 chr6: 32,812,212-32,816,784 , GRCh38.p13 chr6: 32,844,435-32,849,007 PSMB8, TAP1, 1 more genes
    nsv5236657copy number variation1nstd204human GRCh38.p13 chr6: 32,844,154-32,849,392 , GRCh37.p13 chr6: 32,811,931-32,817,169 PSMB8, PSMB8-AS1, 1 more genes
    nsv5224698copy number variation1nstd204human GRCh38.p13 chr6: 32,839,701-32,856,400 , GRCh37.p13 chr6: 32,807,478-32,824,177 PSMB9, PSMB8, 2 more genes
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 ABCF1, ACTG1P9, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 ABCF1, ACTG1P9, 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, ZRF1PS, 1075 more genes
    nsv4675941copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 31,036,397-34,088,832 , GRCh38.p12 chr6: 31,068,620-34,121,055 AGER, AIF1, 219 more genes
    nsv4598541copy number variation1nstd183human GRCh37 chr6: 32,819,110-32,825,125 , GRCh38.p12 chr6: 32,851,333-32,857,348 TAP1, PSMB9
    nsv4592477copy number variation1nstd183human GRCh37 chr6: 32,811,878-32,814,805 , GRCh38.p12 chr6: 32,844,101-32,847,028 TAP1, PSMB8-AS1, 1 more genes
    nsv4382945copy number variation1nstd173human GRCh37 chr6: 32,315,384-33,052,094 , GRCh38.p12 chr6: 32,347,607-33,084,317 HLA-DRB1, RPL32P1, 35 more genes
    nsv4381819copy number variation1nstd173human GRCh37 chr6: 32,315,654-32,857,364 , GRCh38.p12 chr6: 32,347,877-32,889,587 LOC102725019, MTCO3P1, 26 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 RPL35AP18, LOC100421517, 1016 more genes
    nsv3959229copy number variation1nstd168human GRCh38 chr6: 32,787,838-32,849,403 , GRCh37.p13 chr6: 32,755,615-32,817,180 PSMB8, TAP2, 3 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 LOC102724851, FGFR3P1, 1426 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 H4C3, RPL17P25, 2989 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 CNPY3, CT69, 2989 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 LOC105375024, SCIRT, 2995 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 LOC105374992, LOC105374995, 2999 more genes
    nsv3169066inversion1nstd158human GRCh37 chr6: 5,923,377-99,717,885 , GRCh38.p12 chr6: 5,923,144-99,270,009 , ABCF1, 1877 more genes
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