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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5900259copy number variation1nstd209human GRCh38 chr6: 39,905,999-39,906,090 , GRCh37.p13 chr6: 39,873,775-39,873,866 MOCS1
    nsv5845500copy number variation1nstd209human GRCh38 chr6: 39,918,251-39,939,181 , GRCh37.p13 chr6: 39,885,995-39,906,920 MOCS1, LOC102723789
    nsv5844894copy number variation1nstd209human GRCh38 chr6: 39,913,751-39,917,500 , GRCh37.p13 chr6: 39,881,495-39,885,244 MOCS1
    nsv5636887insertion1nstd207human GRCh38 chr6: 39,926,747-39,926,747 , GRCh37.p13 chr6: 39,894,491-39,894,491 MOCS1
    nsv5636112insertion1nstd207human GRCh38 chr6: 39,906,030-39,906,030 , GRCh37.p13 chr6: 39,873,806-39,873,806 MOCS1
    nsv5564438copy number variation1nstd102humanUncertain significance GRCh37 chr6: 39,876,803-39,902,176 , GRCh38.p12 chr6: 39,909,027-39,934,437 MOCS1, LOC102723789
    nsv5468425copy number variation1nstd206human GRCh38 chr6: 39,905,999-39,906,091 , GRCh37.p13 chr6: 39,873,775-39,873,867 MOCS1
    nsv5381624copy number variation1nstd102humanUncertain significance GRCh37 chr6: 39,881,041-39,902,176 , GRCh38.p12 chr6: 39,913,297-39,934,437 MOCS1, LOC102723789
    nsv5031134inversion1nstd200human GRCh38 chr6: 35,178,266-40,407,996 , GRCh37.p13 chr6: 35,146,043-40,375,735 , LOC105375040, 114 more genes
    nsv4872414inversion1nstd200human GRCh37 chr6: 35,146,053-40,375,735 , GRCh38.p12 chr6: 35,178,276-40,407,996 , RPL36P9, 114 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
    nsv4755375insertion1nstd199human GRCh37 chr6: 39,873,835-39,873,835 , GRCh38.p12 chr6: 39,906,059-39,906,059 MOCS1
    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
    nsv4649218copy number variation1nstd186human GRCh37 chr6: 39,873,775-39,873,867 , GRCh38.p12 chr6: 39,905,999-39,906,091 MOCS1
    nsv4522847copy number variation1nstd166human GRCh37.p13 chr6: 39,873,775-39,873,867 , GRCh38.p12 chr6: 39,905,999-39,906,091 MOCS1
    nsv4455638copy number variation1nstd102humanUncertain significance GRCh37 chr6: 39,895,018-39,942,774 , GRCh38.p12 chr6: 39,927,279-39,975,035 LOC102723789, MOCS1, 1 more genes
    nsv4439741insertion1nstd175human GRCh37 chr6: 39,894,489-39,894,489 , GRCh38.p12 chr6: 39,926,745-39,926,745 MOCS1
    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
    nsv3957000insertion1nstd168human GRCh38 chr6: 39,917,909-39,939,265 , GRCh37.p13 chr6: 39,885,653-39,907,004 LOC102723789, MOCS1
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