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Items: 1 to 20 of 268

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5886920copy number variation1nstd209human GRCh38 chr1: 90,921,984-90,922,049 , GRCh37.p13 chr1: 91,387,541-91,387,606 ZNF644
    nsv5874088copy number variation1nstd209human GRCh38 chr1: 90,927,082-90,927,138 , GRCh37.p13 chr1: 91,392,639-91,392,695 ZNF644
    nsv5618715insertion1nstd207human GRCh38 chr1: 90,950,292-90,950,292 , GRCh37.p13 chr1: 91,415,849-91,415,849 ZNF644
    nsv5611788insertion1nstd207human GRCh38 chr1: 90,950,319-90,950,319 , GRCh37.p13 chr1: 91,415,876-91,415,876 ZNF644
    nsv5608151insertion1nstd207human GRCh38 chr1: 90,950,307-90,950,307 , GRCh37.p13 chr1: 91,415,864-91,415,864 ZNF644
    nsv5534522insertion1nstd206human GRCh38 chr1: 90,972,367-90,972,371 , GRCh37.p13 chr1: 91,437,924-91,437,928 ZNF644
    nsv5433035copy number variation1nstd206human GRCh38 chr1: 90,946,732-90,949,181 , GRCh37.p13 chr1: 91,412,289-91,414,738 ZNF644
    nsv5423880copy number variation1nstd206human GRCh38 chr1: 90,987,684-90,987,742 , GRCh37.p13 chr1: 91,453,241-91,453,299 ZNF644
    nsv5420094copy number variation1nstd206human GRCh38 chr1: 90,927,095-90,927,208 , GRCh37.p13 chr1: 91,392,652-91,392,765 ZNF644
    nsv5353566translocation1nstd200human GRCh38 chr1: 90,927,095-90,927,095 , GRCh38 chr1: 90,927,208-90,927,208 , GRCh37.p13 chr1: 91,392,765-91,392,765 , GRCh37.p13 chr1: 91,392,652-91,392,652 ZNF644
    nsv5344908translocation1nstd200human GRCh37 chr1: 91,387,607-91,387,607 , GRCh37 chr1: 91,387,544-91,387,544 , GRCh38.p12 chr1: 90,922,050-90,922,050 , GRCh38.p12 chr1: 90,921,987-90,921,987 ZNF644
    nsv5338569translocation1nstd200human GRCh37 chr1: 91,392,696-91,392,696 , GRCh37 chr1: 91,392,640-91,392,640 , GRCh38.p12 chr1: 90,927,139-90,927,139 , GRCh38.p12 chr1: 90,927,083-90,927,083 ZNF644
    nsv5077926mobile element insertion1nstd203human GRCh38 chr1: 90,958,896-90,958,898 , GRCh37.p13 chr1: 91,424,453-91,424,455 ZNF644
    nsv5062122mobile element insertion1nstd203human GRCh38 chr1: 90,927,654-90,927,669 , GRCh37.p13 chr1: 91,393,211-91,393,226 ZNF644
    nsv4896932copy number variation1nstd200human GRCh38 chr1: 90,993,618-91,001,636 , GRCh37.p13 chr1: 91,459,175-91,467,193 ZNF644
    nsv4896931copy number variation1nstd200human GRCh38 chr1: 90,988,327-90,988,377 , GRCh37.p13 chr1: 91,453,884-91,453,934 ZNF644
    nsv4888344inversion1nstd200human GRCh37 chr1: 51,769,169-94,478,994 , GRCh38.p12 chr1: 51,303,497-94,013,438 , ST13P20, 664 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4759437insertion1nstd199human GRCh37 chr1: 91,415,838-91,415,838 , GRCh38.p12 chr1: 90,950,281-90,950,281 ZNF644
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