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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5896771copy number variation1nstd209human GRCh38 chr6: 33,912,123-33,912,174 , GRCh37.p13 chr6: 33,879,900-33,879,951 LOC105375026
    nsv5896718copy number variation1nstd209human GRCh38 chr6: 33,903,867-33,935,725 , GRCh37.p13 chr6: 33,871,644-33,903,502 LOC107986590, LOC105375026
    nsv5845249copy number variation1nstd209human GRCh38 chr6: 33,903,867-33,911,126 , GRCh37.p13 chr6: 33,871,644-33,878,903 LOC107986590, LOC105375026
    nsv5691299mobile element insertion1nstd211human GRCh38 chr6: 33,897,381-33,897,381 , GRCh37.p13 chr6: 33,865,158-33,865,158 LINC01016, MIR7159, 1 more genes
    nsv5465133copy number variation1nstd206human GRCh38 chr6: 33,897,799-33,898,726 , GRCh37.p13 chr6: 33,865,576-33,866,503 LOC105375026, MIR7159
    nsv5378383translocation1nstd200human GRCh38 chr6: 33,906,690-33,906,690 , GRCh38 chr6: 33,907,057-33,907,057 , GRCh37.p13 chr6: 33,874,834-33,874,834 , GRCh37.p13 chr6: 33,874,467-33,874,467 LOC105375026
    nsv5378381translocation1nstd200human GRCh38 chr6: 33,906,602-33,906,602 , GRCh38 chr6: 33,908,728-33,908,728 , GRCh37.p13 chr6: 33,876,505-33,876,505 , GRCh37.p13 chr6: 33,874,379-33,874,379 LOC105375026
    nsv4940786copy number variation1nstd200human GRCh38 chr6: 33,904,650-33,906,687 , GRCh37.p13 chr6: 33,872,427-33,874,464 LOC107986590, LOC105375026
    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
    nsv4675941copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 31,036,397-34,088,832 , GRCh38.p12 chr6: 31,068,620-34,121,055 AGER, AIF1, 217 more genes
    nsv4523071copy number variation1nstd166human GRCh37.p13 chr6: 33,874,834-33,876,546 , GRCh38.p12 chr6: 33,907,057-33,908,769 LOC105375026
    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
    nsv4332466sequence alteration1nstd166human GRCh37.p13 chr6: 33,872,427-33,876,504 , GRCh38.p12 chr6: 33,904,650-33,908,727 LOC105375026, LOC107986590
    nsv4126637copy number variation1nstd166human GRCh37.p13 chr6: 33,872,427-33,874,464 , GRCh38.p12 chr6: 33,904,650-33,906,687 LOC107986590, LOC105375026
    nsv3924793copy number variation1nstd102humanUncertain significance NCBI36 chr6: 33,912,089-34,252,040 , GRCh37 chr6: 33,804,111-34,144,062 , GRCh38 chr6: 33,836,334-34,176,285 MIR7159, LOC105375027, 5 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 TRR-ACG1-2, TMEM217, 1385 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
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