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Items: 1 to 20 of 101

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097337copy number variation1nstd102humanPathogenic GRCh37 chr6: 51,483,879-51,949,731 , GRCh38.p12 chr6: 51,619,081-52,084,933 LOC101927082, LOC105375087, 2 more genes
    nsv7056672inversion1nstd229human GRCh38 chr6: 51,226,717-52,446,371 , GRCh37.p13 chr6: 51,095,293-52,311,169 MIR206, LOC101927082, 16 more genes
    nsv6792102copy number variation1nstd229human GRCh38 chr6: 51,943,801-51,976,700 , GRCh37.p13 chr6: 51,808,599-51,841,498 RN7SL580P, PKHD1
    nsv6789534copy number variation1nstd229human GRCh38 chr6: 51,967,192-51,977,720 , GRCh37.p13 chr6: 51,831,990-51,842,518 PKHD1, RN7SL580P
    nsv6784375copy number variation1nstd229human GRCh38 chr6: 51,945,370-52,013,731 , GRCh37.p13 chr6: 51,810,168-51,878,529 PKHD1, RN7SL580P
    nsv6783962copy number variation1nstd229human GRCh38 chr6: 51,971,400-51,977,156 , GRCh37.p13 chr6: 51,836,198-51,841,954 PKHD1, RN7SL580P
    nsv6780101copy number variation1nstd229human GRCh38 chr6: 51,942,801-51,979,700 , GRCh37.p13 chr6: 51,807,599-51,844,498 RN7SL580P, PKHD1
    nsv6414097copy number variation1nstd223human GRCh38 chr6: 51,945,370-52,013,727 , GRCh37.p13 chr6: 51,810,168-51,878,525 PKHD1, RN7SL580P
    nsv6412191copy number variation1nstd223human GRCh38 chr6: 51,974,181-51,974,949 , GRCh37.p13 chr6: 51,838,979-51,839,747 RN7SL580P, PKHD1
    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
    nsv6312043copy number variation1nstd102humanPathogenic GRCh37 chr6: 51,483,869-51,949,741 , GRCh38.p12 chr6: 51,619,071-52,084,943 PKHD1, RN7SL580P, 2 more genes
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv6135848copy number variation1nstd213human GRCh37 chr6: 50,080,000-52,650,001 , GRCh38.p12 chr6: 50,112,287-52,785,203 SLC25A20P1, FTH1P5, 32 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
    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
    nsv4729270copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 48,626,041-55,575,545 , GRCh38.p12 chr6: 48,658,305-55,710,747 CRISP1, SLC25A20P1, 105 more genes
    nsv4685731copy number variation1nstd102humanPathogenic GRCh37 chr6: 51,695,623-52,371,918 , GRCh38.p12 chr6: 51,830,825-52,507,120 TRAM2, SLC25A20P1, 11 more genes
    nsv4457082copy number variation1nstd102humanUncertain significance GRCh37 chr6: 51,637,152-52,303,162 , GRCh38.p12 chr6: 51,772,354-52,438,364 IL17A, PKHD1, 10 more genes
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