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Items: 1 to 20 of 112

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5893768copy number variation1nstd209human GRCh38 chr5: 135,933,751-135,934,106 , GRCh37.p13 chr5: 135,269,440-135,269,795 FBXL21P
    nsv5841675copy number variation1nstd209human GRCh38 chr5: 135,929,768-135,931,403 , GRCh37.p13 chr5: 135,265,457-135,267,092 FBXL21P
    nsv5637967insertion1nstd207human GRCh38 chr5: 135,933,998-135,933,998 , GRCh37.p13 chr5: 135,269,687-135,269,687 FBXL21P
    nsv5462255copy number variation1nstd206human GRCh38 chr5: 135,933,751-135,934,029 , GRCh37.p13 chr5: 135,269,440-135,269,718 FBXL21P
    nsv5387146copy number variation1nstd186human GRCh37 chr5: 135,269,440-135,269,833 , GRCh38.p12 chr5: 135,933,751-135,934,144 FBXL21P
    nsv5386387copy number variation1nstd186human GRCh37 chr5: 135,269,440-135,269,834 , GRCh38.p12 chr5: 135,933,751-135,934,145 FBXL21P
    nsv5312102copy number variation1nstd204human GRCh38.p13 chr5: 135,933,741-135,934,154 , GRCh37.p13 chr5: 135,269,430-135,269,843 FBXL21P
    nsv5038943inversion1nstd200human GRCh38 chr5: 135,468,456-136,310,303 , GRCh37.p13 chr5: 134,804,146-135,645,991 SMAD5, SMAD5-AS1, 15 more genes
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4945105copy number variation1nstd200human GRCh38 chr5: 135,933,751-135,934,144 , GRCh37.p13 chr5: 135,269,440-135,269,833 FBXL21P
    nsv4938731copy number variation1nstd200human GRCh38 chr5: 135,938,637-135,943,039 , GRCh37.p13 chr5: 135,274,326-135,278,728 FBXL21P
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4805847copy number variation1nstd200human GRCh37 chr5: 135,269,440-135,269,834 , GRCh38.p12 chr5: 135,933,751-135,934,145 FBXL21P
    nsv4804076copy number variation1nstd200human GRCh37 chr5: 135,274,326-135,278,728 , GRCh38.p12 chr5: 135,938,637-135,943,039 FBXL21P
    nsv4561332mobile element insertion1nstd166human GRCh37.p13 chr5: 135,275,804-135,275,804 , GRCh38.p12 chr5: 135,940,115-135,940,115 FBXL21P
    nsv4497315mobile element insertion1nstd166human GRCh37.p13 chr5: 135,275,202-135,275,202 , GRCh38.p12 chr5: 135,939,513-135,939,513 FBXL21P
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4320566inversion1nstd166human GRCh37.p13 chr5: 114,283,102-148,759,757 , GRCh38.p12 chr5: 114,947,405-149,380,194 , ACTBP4, 606 more genes
    nsv3971975copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 126,377,719-136,270,989 , GRCh38.p12 chr5: 127,042,027-136,935,300 ACTBP4, CAMLG, 157 more genes
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