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Items: 1 to 20 of 208

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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
    nsv4969110copy number variation1nstd200human GRCh38 chr8: 15,790,559-16,415,221 , GRCh37.p13 chr8: 15,648,068-16,272,730 CCT3P1, MSR1, 4 more genes
    nsv4969107copy number variation1nstd200human GRCh38 chr8: 15,441,140-15,812,860 , GRCh37.p13 chr8: 15,298,649-15,670,369 PPM1AP1, LOC100431174, 1 more genes
    nsv4825641copy number variation1nstd200human GRCh37 chr8: 15,648,068-16,272,730 , GRCh38.p12 chr8: 15,790,559-16,415,221 MSR1, MRPL49P2, 4 more genes
    nsv4728911copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,528,482-29,886,483 , GRCh38.p12 chr8: 12,670,973-30,028,967 NAT1, NAT2, 272 more genes
    nsv4679591copy number variation1nstd189human GRCh38.p12 chr8: 15,722,383-15,911,607 , GRCh37.p13 chr8: 15,579,892-15,769,116 TUSC3, PPM1AP1
    nsv4675451copy number variation1nstd102humanUncertain significance GRCh37 chr8: 15,607,855-15,935,440 , GRCh38.p12 chr8: 15,750,346-16,077,931 RPL32P19, PPM1AP1, 1 more genes
    nsv4613305copy number variation1nstd183human GRCh37 chr8: 15,547,450-15,669,601 , GRCh38.p12 chr8: 15,689,941-15,812,092 TUSC3, LOC100431174, 1 more genes
    nsv4605353copy number variation1nstd183human GRCh37 chr8: 14,836,265-16,162,075 , GRCh38.p12 chr8: 14,978,756-16,304,566 MSR1, TUSC3, 5 more genes
    nsv4603812copy number variation1nstd183human GRCh37 chr8: 15,664,027-15,714,840 , GRCh38.p12 chr8: 15,806,518-15,857,331 PPM1AP1
    nsv4525445copy number variation1nstd166human GRCh37.p13 chr8: 14,300,997-16,419,000 , GRCh38.p12 chr8: 14,443,488-16,561,491 LOC100431174, CCT3P1, 9 more genes
    nsv4524760copy number variation1nstd166human GRCh37.p13 chr8: 15,644,499-15,764,000 , GRCh38.p12 chr8: 15,786,990-15,906,491 PPM1AP1
    nsv4456945copy number variation1nstd102humanUncertain significance GRCh37 chr8: 14,515,179-16,846,319 , GRCh38.p12 chr8: 14,657,670-16,988,810 MRPL49P2, LOC101929028, 10 more genes
    nsv4397309copy number variation1nstd174human GRCh37 chr8: 15,649,603-16,356,154 , GRCh38.p12 chr8: 15,792,094-16,498,645 MSR1, PPM1AP1, 4 more genes
    nsv4396939copy number variation1nstd174human GRCh37 chr8: 15,642,213-15,885,126 , GRCh38.p12 chr8: 15,784,704-16,027,617 PPM1AP1, RPL32P19
    nsv4393715copy number variation1nstd174human GRCh37 chr8: 15,493,122-15,669,601 , GRCh38.p12 chr8: 15,635,613-15,812,092 PPM1AP1, TUSC3, 1 more genes
    nsv4374556copy number variation1nstd173human GRCh37 chr8: 15,512,688-16,278,556 , GRCh38.p12 chr8: 15,655,179-16,421,047 CCT3P1, MRPL49P2, 6 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
    nsv4348018copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,546,855-35,816,855 , GRCh38.p12 chr8: 12,689,346-35,959,337 NAT1, NAT2, 343 more genes
    nsv4169050copy number variation1nstd166human GRCh37.p13 chr8: 15,644,689-15,685,083 , GRCh38.p12 chr8: 15,787,180-15,827,574 PPM1AP1
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