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Items: 1 to 20 of 533

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964435insertion1nstd209human GRCh38 chr2: 158,550,142-158,550,142 , GRCh37.p13 chr2: 159,406,654-159,406,654 PKP4
    nsv5900612copy number variation1nstd209human GRCh38 chr2: 158,548,494-158,548,640 , GRCh37.p13 chr2: 159,405,006-159,405,152 RPL7AP22, PKP4
    nsv5897508copy number variation1nstd209human GRCh38 chr2: 158,554,009-158,554,211 , GRCh37.p13 chr2: 159,410,521-159,410,723 PKP4
    nsv5890169copy number variation1nstd209human GRCh38 chr2: 158,501,698-158,501,757 , GRCh37.p13 chr2: 159,358,210-159,358,269 PKP4
    nsv5729884mobile element insertion1nstd211human GRCh38 chr2: 158,528,649-158,528,649 , GRCh37.p13 chr2: 159,385,161-159,385,161 PKP4
    nsv5723497mobile element insertion1nstd211human GRCh38 chr2: 158,587,603-158,587,603 , GRCh37.p13 chr2: 159,444,115-159,444,115 PKP4, LOC105373715
    nsv5683189mobile element insertion1nstd211human GRCh38 chr2: 158,628,450-158,628,450 , GRCh37.p13 chr2: 159,484,962-159,484,962 PKP4
    nsv5681957mobile element insertion1nstd211human GRCh38 chr2: 158,489,799-158,489,799 , GRCh37.p13 chr2: 159,346,311-159,346,311 PKP4
    nsv5674509mobile element insertion1nstd211human GRCh38 chr2: 158,482,524-158,482,524 , GRCh37.p13 chr2: 159,339,036-159,339,036 PKP4
    nsv5621286insertion1nstd207human GRCh38 chr2: 158,550,141-158,550,141 , GRCh37.p13 chr2: 159,406,653-159,406,653 PKP4
    nsv5616104insertion1nstd207human GRCh38 chr2: 158,501,698-158,501,698 , GRCh37.p13 chr2: 159,358,210-159,358,210 PKP4
    nsv5608117insertion1nstd207human GRCh38 chr2: 158,548,494-158,548,494 , GRCh37.p13 chr2: 159,405,006-159,405,006 RPL7AP22, PKP4
    nsv5563729mobile element insertion1nstd206human GRCh38 chr2: 158,587,603-158,587,654 , GRCh37.p13 chr2: 159,444,115-159,444,166 PKP4, LOC105373715
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5547294insertion1nstd206human GRCh38 chr2: 158,678,836-158,678,885 , GRCh37.p13 chr2: 159,535,348-159,535,397 PKP4, PKP4-AS1
    nsv5453303copy number variation1nstd206human GRCh38 chr2: 158,548,494-158,548,644 , GRCh37.p13 chr2: 159,405,006-159,405,156 RPL7AP22, PKP4
    nsv5451265copy number variation1nstd206human GRCh38 chr2: 158,459,370-158,462,801 , GRCh37.p13 chr2: 159,315,882-159,319,313 PKP4
    nsv5442042copy number variation1nstd206human GRCh38 chr2: 158,458,971-158,465,944 , GRCh37.p13 chr2: 159,315,483-159,322,456 PKP4
    nsv5437990copy number variation1nstd206human GRCh38 chr2: 158,458,357-158,458,826 , GRCh37.p13 chr2: 159,314,869-159,315,338 PKP4
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