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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5443004copy number variation1nstd206human GRCh38 chr2: 74,668,936-75,021,425 , GRCh37.p13 chr2: 74,896,063-75,248,552 , POLE4, 8 more genes
    nsv5300067copy number variation1nstd204human GRCh38.p13 chr2: 74,921,327-75,014,271 , GRCh37.p13 chr2: 75,148,454-75,241,398 LINC01291, POLE4, 2 more genes
    nsv5211282copy number variation1nstd204human GRCh38.p13 chr2: 74,955,685-75,007,171 , GRCh37.p13 chr2: 75,182,812-75,234,298 POLE4, LOC105374809
    nsv5211003copy number variation1nstd204human GRCh38.p13 chr2: 74,955,685-74,962,655 , GRCh37.p13 chr2: 75,182,812-75,189,782 LOC105374809, POLE4
    nsv5210870copy number variation1nstd204human GRCh38.p13 chr2: 74,933,201-75,014,500 , GRCh37.p13 chr2: 75,160,328-75,241,627 LINC01293, LOC105374809, 2 more genes
    nsv5190837mobile element insertion1nstd203human GRCh38 chr2: 74,967,696-74,967,710 , GRCh37.p13 chr2: 75,194,823-75,194,837 POLE4
    nsv5068291mobile element insertion1nstd203human GRCh38 chr2: 74,957,870-74,957,879 , GRCh37.p13 chr2: 75,184,997-75,185,006 POLE4, LOC105374809
    nsv4908829copy number variation1nstd200human GRCh38 chr2: 74,921,354-75,014,244 , GRCh37.p13 chr2: 75,148,481-75,241,371 POLE4, LINC01291, 2 more genes
    nsv4908828copy number variation1nstd200human GRCh38 chr2: 74,889,407-75,041,729 , GRCh37.p13 chr2: 75,116,534-75,268,856 LINC01293, LOC105374809, 3 more genes
    nsv4908826copy number variation1nstd200human GRCh38 chr2: 74,725,737-74,958,478 , GRCh37.p13 chr2: 74,952,864-75,185,605 LOC102724482, HK2, 6 more genes
    nsv4908825copy number variation1nstd200human GRCh38 chr2: 74,722,485-75,154,898 , GRCh37.p13 chr2: 74,949,612-75,382,024 LOC105374811, LOC102724482, 9 more genes
    nsv4908823copy number variation1nstd200human GRCh38 chr2: 74,593,093-75,089,577 , GRCh37.p13 chr2: 74,820,220-75,316,704 , LOC105374809, 13 more genes
    nsv4901951copy number variation1nstd200human GRCh38 chr2: 74,967,269-74,968,656 , GRCh37.p13 chr2: 75,194,396-75,195,783 POLE4
    nsv4781581copy number variation1nstd200human GRCh37 chr2: 75,148,481-75,241,371 , GRCh38.p12 chr2: 74,921,354-75,014,244 POLE4, LINC01291, 2 more genes
    nsv4781579copy number variation1nstd200human GRCh37 chr2: 75,116,534-75,268,856 , GRCh38.p12 chr2: 74,889,407-75,041,729 LINC01291, HK2, 3 more genes
    nsv4781578copy number variation1nstd200human GRCh37 chr2: 74,949,612-75,382,024 , GRCh38.p12 chr2: 74,722,485-75,154,898 HK2, MIR5000, 9 more genes
    nsv4728304copy number variation1nstd102humanUncertain significance GRCh37 chr2: 74,780,969-75,444,113 , GRCh38.p12 chr2: 74,553,842-75,216,987 TVP23BP2, LOC105374809, 15 more genes
    nsv4728163copy number variation1nstd102humanLikely benign GRCh37 chr2: 74,825,161-75,308,974 , GRCh38.p12 chr2: 74,598,034-75,081,847 LOC102724482, LOC102724497, 11 more genes
    nsv4680988copy number variation1nstd189human GRCh37.p13 chr2: 74,933,879-75,229,934 , GRCh38.p12 chr2: 74,706,752-75,002,807 , HK2, 7 more genes
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