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Items: 1 to 20 of 167

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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
    nsv6867252copy number variation1nstd229human GRCh38 chr8: 134,840,046-134,857,039 , GRCh37.p13 chr8: 135,852,289-135,869,282 LOC101927845, NCRNA00250
    nsv6864457copy number variation1nstd229human GRCh38 chr8: 134,842,596-134,845,644 , GRCh37.p13 chr8: 135,854,839-135,857,887 NCRNA00250
    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
    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
    nsv6632322copy number variation1nstd224human GRCh37 chr8: 135,855,079-135,882,012 , GRCh38.p12 chr8: 134,842,836-134,869,769 NCRNA00250, LOC101927845
    nsv6433594copy number variation1nstd223human GRCh38 chr8: 134,832,601-134,836,600 , GRCh37.p13 chr8: 135,844,844-135,848,843 NCRNA00250
    nsv6424785copy number variation1nstd223human GRCh38 chr8: 134,837,826-134,870,392 , GRCh37.p13 chr8: 135,850,069-135,882,635 LOC101927845, NCRNA00250
    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
    nsv6246697mobile element insertion1nstd215human GRCh38 chr8: 134,836,544-134,836,544 , GRCh37.p13 chr8: 135,848,787-135,848,787 NCRNA00250
    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
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