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Items: 1 to 20 of 284

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966724insertion1nstd209human GRCh38 chr6: 31,498,593-31,498,593 , GRCh37.p13 chr6: 31,466,370-31,466,370 MICB
    nsv5906090copy number variation1nstd209human GRCh38 chr6: 31,410,306-31,505,274 , GRCh37.p13 chr6: 31,378,083-31,473,051 MICB, HCP5, 5 more genes
    nsv5901262copy number variation1nstd209human GRCh38 chr6: 31,400,855-31,495,065 , GRCh37.p13 chr6: 31,368,632-31,462,842 MICB, HCP5, 6 more genes
    nsv5897239copy number variation1nstd209human GRCh38 chr6: 31,498,988-31,499,044 , GRCh37.p13 chr6: 31,466,765-31,466,821 MICB
    nsv5845232copy number variation1nstd209human GRCh38 chr6: 31,496,585-31,501,467 , GRCh37.p13 chr6: 31,464,362-31,469,244 MICB
    nsv5845131copy number variation1nstd209human GRCh38 chr6: 31,488,419-31,494,834 , GRCh37.p13 chr6: 31,456,196-31,462,611 MICB-DT, MICB
    nsv5680437mobile element insertion1nstd211human GRCh38 chr6: 31,502,943-31,502,943 , GRCh37.p13 chr6: 31,470,720-31,470,720 MICB
    nsv5643641insertion1nstd207human GRCh38 chr6: 31,498,593-31,498,593 , GRCh37.p13 chr6: 31,466,370-31,466,370 MICB
    nsv5574365copy number variation1nstd207human GRCh38 chr6: 31,498,988-31,499,044 , GRCh37.p13 chr6: 31,466,765-31,466,821 MICB
    nsv5552839insertion1nstd206human GRCh38 chr6: 31,498,593-31,498,593 , GRCh37.p13 chr6: 31,466,370-31,466,370 MICB
    nsv5463152copy number variation1nstd206human GRCh38 chr6: 31,493,115-31,498,087 , GRCh37.p13 chr6: 31,460,892-31,465,864 MICB, MICB-DT
    nsv5460182copy number variation1nstd206human GRCh38 chr6: 31,493,110-31,495,073 , GRCh37.p13 chr6: 31,460,887-31,462,850 MICB-DT, MICB
    nsv5398356mobile element insertion1nstd206human GRCh38 chr6: 31,502,943-31,502,994 , GRCh37.p13 chr6: 31,470,720-31,470,771 MICB
    nsv5382643mobile element deletion1nstd186human GRCh37 chr6: 31,472,022-31,472,335 , GRCh38.p12 chr6: 31,504,245-31,504,558 MICB
    nsv5378352translocation1nstd200human GRCh38 chr6: 31,402,396-31,402,396 , GRCh38 chr6: 31,496,857-31,496,857 , GRCh37.p13 chr6: 31,464,634-31,464,634 , GRCh37.p13 chr6: 31,370,173-31,370,173 MICA, MICB
    nsv5344592translocation1nstd200human GRCh37 chr6: 31,370,173-31,370,173 , GRCh37 chr6: 31,464,634-31,464,634 , GRCh38.p12 chr6: 31,402,396-31,402,396 , GRCh38.p12 chr6: 31,496,857-31,496,857 MICA, MICB
    nsv5234405copy number variation1nstd204human GRCh38.p13 chr6: 30,240,001-32,313,700 , GRCh37.p13 chr6: 30,207,778-32,281,477 DDAH2, LOC105375018, 175 more genes
    nsv5229879copy number variation1nstd204human GRCh38.p13 chr6: 31,502,001-32,151,900 , GRCh37.p13 chr6: 31,469,778-32,119,677 LTB, PPT2, 80 more genes
    nsv5118587mobile element insertion1nstd203human GRCh38 chr6: 31,498,447-31,498,456 , GRCh37.p13 chr6: 31,466,224-31,466,233 MICB
    nsv5115612mobile element insertion1nstd203human GRCh38 chr6: 31,498,626-31,498,640 , GRCh37.p13 chr6: 31,466,403-31,466,417 MICB
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