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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906086copy number variation1nstd209human GRCh38 chr6: 42,785,329-42,785,825 , GRCh37.p13 chr6: 42,753,067-42,753,563 LOC401261, BICRAL
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5470853copy number variation1nstd206human GRCh38 chr6: 42,783,355-42,783,443 , GRCh37.p13 chr6: 42,751,093-42,751,181 BICRAL, LOC401261
    nsv5224950copy number variation1nstd204human GRCh38.p13 chr6: 42,543,301-43,041,600 , GRCh37.p13 chr6: 42,511,039-43,009,338 , RPL7L1, 20 more genes
    nsv5221097copy number variation1nstd204human GRCh38.p13 chr6: 42,781,801-42,843,700 , GRCh37.p13 chr6: 42,749,539-42,811,438 BICRAL, LOC401261
    nsv4941122copy number variation1nstd200human GRCh38 chr6: 42,784,067-42,785,459 , GRCh37.p13 chr6: 42,751,805-42,753,197 LOC401261, BICRAL
    nsv4816189copy number variation1nstd200human GRCh37 chr6: 42,751,805-42,753,197 , GRCh38.p12 chr6: 42,784,067-42,785,459 LOC401261, BICRAL
    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
    nsv4593609copy number variation1nstd183human GRCh37 chr6: 42,742,307-42,750,036 , GRCh38.p12 chr6: 42,774,569-42,782,298 LOC401261, BICRAL
    nsv4592683copy number variation1nstd183human GRCh37 chr6: 42,627,455-43,357,404 , GRCh38.p12 chr6: 42,659,717-43,389,666 , PEX6, 36 more genes
    nsv4559701mobile element insertion1nstd166human GRCh37.p13 chr6: 42,758,352-42,758,352 , GRCh38.p12 chr6: 42,790,614-42,790,614 BICRAL, LOC401261
    nsv4523001copy number variation1nstd166human GRCh37.p13 chr6: 42,753,270-42,753,925 , GRCh38.p12 chr6: 42,785,532-42,786,187 LOC401261, BICRAL
    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
    nsv4134478copy number variation1nstd166human GRCh37.p13 chr6: 42,753,057-42,753,623 , GRCh38.p12 chr6: 42,785,319-42,785,885 LOC401261, BICRAL
    nsv3969370copy number variation1nstd168human GRCh38 chr6: 42,774,374-42,898,769 , GRCh37.p13 chr6: 42,742,112-42,866,507 , C6orf226, 3 more genes
    nsv3924318copy number variation1nstd102humanPathogenic GRCh37 chr6: 42,336,296-44,558,281 , NCBI36 chr6: 42,444,274-44,666,259 , GRCh38 chr6: 42,368,558-44,590,544 MIR4642, SRF, 82 more genes
    nsv3919521copy number variation1nstd102humanPathogenic NCBI36 chr6: 37,853,123-45,729,558 , GRCh37 chr6: 37,745,145-45,621,580 , GRCh38 chr6: 37,777,369-45,653,843 RPL23P6, LOC102723789, 184 more genes
    nsv3919402copy number variation1nstd102humanPathogenic NCBI36 chr6: 42,769,519-46,417,784 , GRCh37.p13 chr6: 42,661,541-46,309,825 , GRCh38.p12 chr6: 42,693,803-46,342,088 LOC101929770, MRPS18A, 94 more genes
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