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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148238copy number variation1nstd102humanPathogenic GRCh38 chr8: 115,586,904-135,607,135 , GRCh37.p13 chr8: 116,599,131-136,619,378 CCDC26, EFR3A, 238 more genes
    nsv7148132copy number variation1nstd102humanPathogenic GRCh37 chr8: 131,138,343-143,473,913 , GRCh38.p12 chr8: 130,126,097-142,392,552 LOC107983985, MIR30DHG, 104 more genes
    nsv6868534copy number variation1nstd229human GRCh38 chr8: 134,813,969-134,820,320 , GRCh37.p13 chr8: 135,826,212-135,832,563 MIR30DHG
    nsv6841646copy number variation1nstd229human GRCh38 chr8: 133,664,760-134,825,246 , GRCh37.p13 chr8: 134,677,003-135,837,489 ZFAT, LINC03024, 9 more genes
    nsv6841401copy number variation1nstd229human GRCh38 chr8: 133,010,316-136,879,429 , GRCh37.p13 chr8: 134,022,561-137,891,672 LOC107986978, LOC101927822, 35 more genes
    nsv6839883copy number variation1nstd229human GRCh38 chr8: 133,763,935-134,799,914 , GRCh37.p13 chr8: 134,776,178-135,812,157 LOC101927798, MIR30DHG, 5 more genes
    nsv6637931copy number variation1nstd102humanUncertain significance GRCh37 chr8: 134,229,655-137,934,713 , GRCh38.p12 chr8: 133,217,412-136,922,470 KHDRBS3, LINC03024, 28 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6571657inversion1nstd223human GRCh38 chr8: 134,812,435-134,813,607 , GRCh37.p13 chr8: 135,824,678-135,825,850 MIR30DHG
    nsv6422056copy number variation1nstd223human GRCh38 chr8: 134,798,201-134,799,100 , GRCh37.p13 chr8: 135,810,444-135,811,343 MIR30DHG, MIR30B
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
    nsv6314744copy number variation1nstd102humanPathogenic GRCh37 chr8: 96,496,503-146,295,711 , GRCh38.p12 chr8: 95,484,275-145,070,325 OSR2, LOC392268, 676 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6313487copy number variation1nstd102humanPathogenic GRCh37 chr8: 130,863,093-146,295,771 , GRCh38.p12 chr8: 129,850,847-145,070,385 LOC105375784, CYP11B2, 253 more genes
    nsv6290242copy number variation1nstd102humanUncertain significance GRCh37 chr8: 128,878,931-141,662,233 , GRCh38.p12 chr8: 127,866,685-140,652,134 LINC02055, LOC101927798, 100 more genes
    nsv6136329copy number variation1nstd213human GRCh37 chr8: 135,550,000-136,160,001 , GRCh38.p12 chr8: 134,537,757-135,147,758 ZFAT, MIR30B, 6 more genes
    nsv6136253copy number variation1nstd213human GRCh37 chr8: 135,020,000-135,930,001 , GRCh38.p12 chr8: 134,007,757-134,917,758 ZFAT, MIR30B, 5 more genes
    nsv6136082copy number variation1nstd213human GRCh37 chr8: 86,730,000-142,740,001 , GRCh38.p12 chr8: 85,717,771-141,729,803 ANXA13, ATP6V1C1, 658 more genes
    nsv6136008copy number variation1nstd213human GRCh37 chr8: 135,250,000-137,550,001 , GRCh38.p12 chr8: 134,237,757-136,537,758 ZFAT, MAPRE1P1, 15 more genes
    nsv6136003copy number variation1nstd213human GRCh37 chr8: 133,920,000-137,040,001 , GRCh38.p12 chr8: 132,907,755-136,027,758 SLA, RPL32P20, 33 more genes
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