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Items: 1 to 20 of 356

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970929insertion1nstd209human GRCh38 chr12: 50,383,278-50,383,278 , GRCh37.p13 chr12: 50,777,061-50,777,061 FAM186A
    nsv5939238copy number variation1nstd209human GRCh38 chr12: 50,255,984-50,346,488 , GRCh37.p13 chr12: 50,649,767-50,740,271 RNU6-1093P, LOC100418734, 3 more genes
    nsv5937680copy number variation1nstd209human GRCh38 chr12: 50,358,863-50,359,337 , GRCh37.p13 chr12: 50,752,646-50,753,120 FAM186A
    nsv5936213copy number variation1nstd209human GRCh38 chr12: 50,384,862-50,391,371 , GRCh37.p13 chr12: 50,778,645-50,785,154 FAM186A
    nsv5930278copy number variation1nstd209human GRCh38 chr12: 50,375,232-50,390,333 , GRCh37.p13 chr12: 50,769,015-50,784,116 FAM186A
    nsv5929461copy number variation1nstd209human GRCh38 chr12: 50,393,918-50,394,222 , GRCh37.p13 chr12: 50,787,701-50,788,005 FAM186A
    nsv5867486copy number variation2nstd209human GRCh38 chr12: 50,384,249-50,390,048 , GRCh37.p13 chr12: 50,778,032-50,783,831 FAM186A
    nsv5856104copy number variation1nstd209human GRCh38 chr12: 50,336,015-50,338,735 , GRCh37.p13 chr12: 50,729,798-50,732,518 FAM186A
    nsv5853301copy number variation1nstd209human GRCh38 chr12: 50,375,221-50,384,548 , GRCh37.p13 chr12: 50,769,004-50,778,331 FAM186A
    nsv5851591copy number variation1nstd209human GRCh38 chr12: 50,378,775-50,381,916 , GRCh37.p13 chr12: 50,772,558-50,775,699 FAM186A
    nsv5725858mobile element insertion1nstd211human GRCh38 chr12: 50,338,711-50,338,711 , GRCh37.p13 chr12: 50,732,494-50,732,494 FAM186A
    nsv5719049mobile element insertion2nstd211human GRCh38 chr12: 50,358,442-50,358,442 , GRCh37.p13 chr12: 50,752,225-50,752,225 FAM186A
    nsv5716440mobile element insertion1nstd211human GRCh38 chr12: 50,386,564-50,386,564 , GRCh37.p13 chr12: 50,780,347-50,780,347 FAM186A
    nsv5645112insertion1nstd207human GRCh38 chr12: 50,352,003-50,352,003 , GRCh37.p13 chr12: 50,745,786-50,745,786 FAM186A
    nsv5512156copy number variation1nstd206human GRCh38 chr12: 50,376,825-50,376,879 , GRCh37.p13 chr12: 50,770,608-50,770,662 FAM186A
    nsv5508478copy number variation1nstd206human GRCh38 chr12: 50,375,232-50,390,334 , GRCh37.p13 chr12: 50,769,015-50,784,117 FAM186A
    nsv5504072copy number variation1nstd206human GRCh38 chr12: 50,372,532-50,372,808 , GRCh37.p13 chr12: 50,766,315-50,766,591 FAM186A
    nsv5497704copy number variation1nstd206human GRCh38 chr12: 50,392,137-50,399,649 , GRCh37.p13 chr12: 50,785,920-50,793,432 FAM186A, LARP4
    nsv5194316mobile element insertion1nstd203human GRCh38 chr12: 50,338,711-50,338,728 , GRCh37.p13 chr12: 50,732,494-50,732,511 FAM186A
    nsv5129831mobile element insertion1nstd203human GRCh38 chr12: 50,374,451-50,374,466 , GRCh37.p13 chr12: 50,768,234-50,768,249 FAM186A
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