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Items: 1 to 20 of 159

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4960216copy number variation1nstd200human GRCh38 chr8: 37,748,384-37,748,502 , GRCh37.p13 chr8: 37,605,902-37,606,020 LOC728024, ERLIN2
    nsv4960215copy number variation1nstd200human GRCh38 chr8: 37,737,128-37,738,419 , GRCh37.p13 chr8: 37,594,646-37,595,937 LOC102723701, ERLIN2
    nsv4827414copy number variation1nstd200human GRCh37 chr8: 37,605,902-37,606,020 , GRCh38.p12 chr8: 37,748,384-37,748,502 ERLIN2, LOC728024
    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
    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
    nsv4456199copy number variation1nstd102humanUncertain significance GRCh37 chr8: 36,094,421-43,822,214 , GRCh38.p12 chr8: 36,236,903-43,967,071 AFG3L2P1, BRF2, 136 more genes
    nsv4436744copy number variation1nstd102humanUncertain significance GRCh37 chr8: 36,486,830-37,992,515 , GRCh38.p12 chr8: 36,629,312-38,134,997 LOC105379380, LOC728024, 29 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4166590copy number variation1nstd166human GRCh37.p13 chr8: 37,591,000-37,597,000 , GRCh38.p12 chr8: 37,733,482-37,739,482 LOC101929622, LOC102723701, 1 more genes
    nsv3923517copy number variation1nstd102humanPathogenic NCBI36 chr8: 36,556,779-60,694,111 , GRCh37 chr8: 36,437,621-60,531,557 , GRCh38 chr8: 36,580,103-59,618,998 LOC105379380, TPT1P8, 320 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
    nsv3922311copy number variation1nstd102humanPathogenic NCBI36 chr8: 37,428,611-47,058,107 , GRCh37.p13 chr8: 37,309,453-46,938,942 , GRCh38.p12 chr8: 37,451,935-46,027,320 CHRNB3, LOC105379380, 120 more genes
    nsv3921773copy number variation1nstd102humanPathogenic NCBI36 chr8: 12,511,855-43,310,472 , GRCh38 chr8: 12,609,975-43,336,172 , GRCh37 chr8: 12,467,484-43,191,315 RPL5P22, ZMAT4, 481 more genes
    nsv3921545copy number variation1nstd102humanPathogenic NCBI36 chr8: 33,964,607-47,058,107 , GRCh37.p13 chr8: 33,845,065-46,938,942 , GRCh38.p12 chr8: 33,987,547-46,027,320 SFRP1, DKK4, 148 more genes
    nsv3921539copy number variation1nstd102humanPathogenic NCBI36 chr8: 153,682-47,058,107 , GRCh37.p13 chr8: 163,682-46,938,942 , GRCh38.p12 chr8: 213,682-46,027,320 HSPD1P3, RNA5SP253, 770 more genes
    nsv3921035copy number variation2nstd102humanPathogenic GRCh38 chr8: 12,728,904-43,673,207 , GRCh37 chr8: 12,586,413-43,528,350 , NCBI36 chr8: 12,630,784-43,647,507 MIR4287, RNU6-533P, 477 more genes
    nsv3920952copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,452-37,879,246 , GRCh38 chr8: 226,452-38,021,728 , NCBI36 chr8: 166,452-37,998,403 MTUS1, LINC00208, 666 more genes
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