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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148130copy number variation1nstd102humanPathogenic GRCh37 chr8: 36,763,176-50,929,707 , GRCh38.p12 chr8: 36,905,658-50,017,147 SNTG1, RN7SL806P, 193 more genes
    nsv6843025copy number variation1nstd229human GRCh38 chr8: 37,730,639-37,733,887 , GRCh37.p13 chr8: 37,588,157-37,591,405 LOC102723701, LOC101929622
    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
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6424090copy number variation1nstd223human GRCh38 chr8: 37,737,128-37,738,419 , GRCh37.p13 chr8: 37,594,646-37,595,937 ERLIN2, LOC102723701
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6312909copy number variation5nstd102humanUncertain significance, Pathogenic GRCh37 chr8: 37,595,441-38,961,219 , GRCh38.p12 chr8: 37,737,923-39,103,700 LSM1, BAG4, 33 more genes
    nsv6291079copy number variation1nstd102humanUncertain significance GRCh37 chr8: 37,544,476-37,818,465 , GRCh38.p12 chr8: 37,686,958-37,960,947 ZNF703, BRF2, 10 more genes
    nsv6137281copy number variation1nstd213human GRCh37 chr8: 37,350,000-38,410,001 , GRCh38.p12 chr8: 37,492,482-38,552,483 ADRB3, EIF4EBP1, 32 more genes
    nsv6136578copy number variation1nstd213human GRCh37 chr8: 37,570,000-37,710,001 , GRCh38.p12 chr8: 37,712,482-37,852,483 ERLIN2, PLPBP, 6 more genes
    nsv5965403insertion1nstd209human GRCh38 chr8: 37,734,482-37,734,482 , GRCh37.p13 chr8: 37,592,000-37,592,000 LOC102723701
    nsv5643983insertion1nstd207human GRCh38 chr8: 37,734,478-37,734,478 , GRCh37.p13 chr8: 37,591,996-37,591,996 LOC102723701
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4960215copy number variation1nstd200human GRCh38 chr8: 37,737,128-37,738,419 , GRCh37.p13 chr8: 37,594,646-37,595,937 LOC102723701, ERLIN2
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 , ADRA1A, 411 more genes
    nsv4756879inversion1nstd199human GRCh37 chr8: 23,474,453-53,323,933 , GRCh38.p12 chr8: 23,616,940-52,411,373 , ADRA1A, 411 more genes
    nsv4703839copy number variation1nstd195human GRCh37 chr8: 37,323,851-37,784,501 , GRCh38.p12 chr8: 37,466,333-37,926,983 LOC101929622, LOC102723701, 14 more genes
    nsv4545294insertion1nstd166human GRCh37.p13 chr8: 37,592,008-37,592,008 , GRCh38.p12 chr8: 37,734,490-37,734,490 LOC102723701
    nsv4544244insertion1nstd166human GRCh37.p13 chr8: 37,591,996-37,591,996 , GRCh38.p12 chr8: 37,734,478-37,734,478 LOC102723701
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
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