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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6856506copy number variation1nstd229human GRCh38 chr8: 32,086,752-32,091,020 , GRCh37.p13 chr8: 31,944,268-31,948,536 NRG1, NRG1-IT1
    nsv6856278copy number variation1nstd229human GRCh38 chr8: 32,109,889-32,117,737 , GRCh37.p13 chr8: 31,967,405-31,975,253 NRG1, NRG1-IT1
    nsv6855407copy number variation1nstd229human GRCh38 chr8: 32,093,908-32,102,020 , GRCh37.p13 chr8: 31,951,424-31,959,536 NRG1-IT1, NRG1
    nsv6851788copy number variation1nstd229human GRCh38 chr8: 32,027,801-32,033,300 , GRCh37.p13 chr8: 31,885,317-31,890,816 NRG1, NRG1-IT1
    nsv6849345copy number variation1nstd229human GRCh38 chr8: 32,071,696-32,071,727 , GRCh37.p13 chr8: 31,929,212-31,929,243 NRG1, NRG1-IT1
    nsv6849124copy number variation1nstd229human GRCh38 chr8: 32,112,501-32,119,100 , GRCh37.p13 chr8: 31,970,017-31,976,616 NRG1, NRG1-IT1
    nsv6846945copy number variation1nstd229human GRCh38 chr8: 32,073,101-32,076,400 , GRCh37.p13 chr8: 31,930,617-31,933,916 NRG1, NRG1-IT1
    nsv6846413copy number variation1nstd229human GRCh38 chr8: 32,094,030-32,094,381 , GRCh37.p13 chr8: 31,951,546-31,951,897 NRG1, NRG1-IT1
    nsv6845828copy number variation1nstd229human GRCh38 chr8: 32,022,301-32,039,600 , GRCh37.p13 chr8: 31,879,817-31,897,116 NRG1-IT1, NRG1
    nsv6845568copy number variation1nstd229human GRCh38 chr8: 32,026,076-32,034,987 , GRCh37.p13 chr8: 31,883,592-31,892,503 NRG1, NRG1-IT1
    nsv6844786copy number variation1nstd229human GRCh38 chr8: 32,086,501-32,088,800 , GRCh37.p13 chr8: 31,944,017-31,946,316 NRG1, NRG1-IT1
    nsv6844526copy number variation1nstd229human GRCh38 chr8: 32,027,780-32,033,353 , GRCh37.p13 chr8: 31,885,296-31,890,869 NRG1-IT1, NRG1
    nsv6843368copy number variation1nstd229human GRCh38 chr8: 31,134,762-32,502,958 , GRCh37.p13 chr8: 30,992,278-32,360,474 NRG1-IT1, NRG1-IT3, 10 more genes
    nsv6841929copy number variation1nstd229human GRCh38 chr8: 32,104,362-32,139,309 , GRCh37.p13 chr8: 31,961,878-31,996,825 NRG1-IT1, NRG1
    nsv6838984copy number variation1nstd229human GRCh38 chr8: 32,092,001-32,107,800 , GRCh37.p13 chr8: 31,949,517-31,965,316 NRG1, NRG1-IT1
    nsv6637025copy number variation1nstd102humanPathogenic GRCh37 chr8: 26,808,969-38,346,383 , GRCh38.p12 chr8: 26,951,452-38,488,865 LINC02948, LOC105379354, 185 more genes
    nsv6636401copy number variation1nstd102humanUncertain significance GRCh37 chr8: 31,406,614-32,010,201 , GRCh38.p12 chr8: 31,549,098-32,152,685 RNA5SP261, NRG1, 1 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6574563inversion1nstd223human GRCh38 chr8: 32,137,168-32,138,866 , GRCh37.p13 chr8: 31,994,684-31,996,382 NRG1, NRG1-IT1
    nsv6572740inversion1nstd223human GRCh38 chr8: 32,090,550-32,091,073 , GRCh37.p13 chr8: 31,948,066-31,948,589 NRG1, NRG1-IT1
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