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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6123124copy number variation1nstd186human GRCh37 chr15: 34,691,063-34,850,075 , GRCh38.p12 chr15: 34,398,862-34,557,874 GOLGA8A, FSCN1P1, 6 more genes
    nsv5945067copy number variation1nstd209human GRCh38 chr15: 34,437,508-34,437,713 , GRCh37.p13 chr15: 34,729,709-34,729,914 GOLGA8A
    nsv5935552copy number variation1nstd209human GRCh38 chr15: 34,437,459-34,583,542 , GRCh37.p13 chr15: 34,729,660-34,875,743 GOLGA8A, FSCN1P1, 5 more genes
    nsv5855991copy number variation3nstd209human GRCh38 chr15: 34,423,612-34,426,333 , GRCh37.p13 chr15: 34,715,813-34,718,534 GOLGA8A
    nsv5853865copy number variation3nstd209human GRCh38 chr15: 34,421,173-34,449,525 , GRCh37.p13 chr15: 34,713,374-34,741,726 GOLGA8A
    nsv5713768mobile element insertion1nstd211human GRCh38 chr15: 34,403,410-34,403,410 , GRCh37.p13 chr15: 34,695,611-34,695,611 GOLGA8A
    nsv5712533mobile element insertion1nstd211human GRCh38 chr15: 34,384,137-34,384,137 , GRCh37.p13 chr15: 34,676,338-34,676,338 GOLGA8A
    nsv5662377insertion1nstd207human GRCh38 chr15: 34,437,425-34,437,425 , GRCh37.p13 chr15: 34,729,626-34,729,626 GOLGA8A
    nsv5659569insertion1nstd207human GRCh38 chr15: 34,419,422-34,419,422 , GRCh37.p13 chr15: 34,711,623-34,711,623 GOLGA8A
    nsv5652006insertion1nstd207human GRCh38 chr15: 34,381,729-34,381,729 , GRCh37.p13 chr15: 34,673,930-34,673,930 GOLGA8A, MIR1233-1
    nsv5603619copy number variation1nstd207human GRCh38 chr15: 34,412,578-34,414,610 , GRCh37.p13 chr15: 34,704,779-34,706,811 GOLGA8A
    nsv5602887copy number variation1nstd207human GRCh38 chr15: 34,437,525-34,437,713 , GRCh37.p13 chr15: 34,729,726-34,729,914 GOLGA8A
    nsv5588254copy number variation1nstd207human GRCh38 chr15: 34,437,425-34,437,475 , GRCh37.p13 chr15: 34,729,626-34,729,676 GOLGA8A
    nsv5585877copy number variation1nstd207human GRCh38 chr15: 34,431,339-34,431,401 , GRCh37.p13 chr15: 34,723,540-34,723,602 GOLGA8A
    nsv5510591copy number variation1nstd206human GRCh38 chr15: 34,398,862-34,557,874 , GRCh37.p13 chr15: 34,691,063-34,850,075 GOLGA8A, FSCN1P1, 6 more genes
    nsv5497794copy number variation1nstd206human GRCh38 chr15: 34,384,155-34,564,874 , GRCh37.p13 chr15: 34,676,356-34,857,075 GOLGA8A, FSCN1P1, 6 more genes
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5357792translocation1nstd200human GRCh38 chr15: 34,522,668-34,522,668 , GRCh38 chr15: 34,379,360-34,379,360 , GRCh37.p13 chr15: 34,671,561-34,671,561 , GRCh37.p13 chr15: 34,814,869-34,814,869 GOLGA8A, DNM1P5
    nsv5332542translocation1nstd200human GRCh37 chr15: 34,729,707-34,729,707 , GRCh37 chr15: 34,729,841-34,729,841 , GRCh38.p12 chr15: 34,437,640-34,437,640 , GRCh38.p12 chr15: 34,437,506-34,437,506 GOLGA8A
    nsv5280167copy number variation1nstd204human GRCh37.p13 chr15: 34,717,402-34,825,801 , GRCh38.p13 chr15: 34,425,201-34,533,600 GOLGA8A, FSCN1P1, 4 more genes
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