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Items: 1 to 20 of 377

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5950920insertion1nstd209human GRCh38 chr1: 92,005,005-92,005,005 , GRCh37.p13 chr1: 92,470,562-92,470,562 BRDT
    nsv5873413copy number variation1nstd209human GRCh38 chr1: 91,943,566-91,947,454 , GRCh37.p13 chr1: 92,409,123-92,413,011 BRDT
    nsv5830848copy number variation1nstd209human GRCh38 chr1: 91,943,592-91,947,402 , GRCh37.p13 chr1: 92,409,149-92,412,959 BRDT
    nsv5692108mobile element insertion1nstd211human GRCh38 chr1: 91,950,708-91,950,708 , GRCh37.p13 chr1: 92,416,265-92,416,265 BRDT
    nsv5688359mobile element insertion2nstd211human GRCh38 chr1: 91,982,750-91,982,750 , GRCh37.p13 chr1: 92,448,307-92,448,307 BRDT
    nsv5676460mobile element insertion1nstd211human GRCh38 chr1: 91,963,804-91,963,804 , GRCh37.p13 chr1: 92,429,361-92,429,361 BRDT
    nsv5676410mobile element insertion2nstd211human GRCh38 chr1: 92,005,018-92,005,018 , GRCh37.p13 chr1: 92,470,575-92,470,575 BRDT
    nsv5569132copy number variation1nstd207human GRCh38 chr1: 91,962,197-91,962,318 , GRCh37.p13 chr1: 92,427,754-92,427,875 BRDT
    nsv5398472mobile element insertion1nstd206human GRCh38 chr1: 92,005,018-92,005,069 , GRCh37.p13 chr1: 92,470,575-92,470,626 BRDT
    nsv5396939mobile element insertion1nstd206human GRCh38 chr1: 91,982,735-91,982,735 , GRCh37.p13 chr1: 92,448,292-92,448,292 BRDT
    nsv5335817translocation1nstd200human GRCh37 chr1: 92,431,375-92,431,375 , GRCh37 chr1: 92,431,518-92,431,518 , GRCh38.p12 chr1: 91,965,961-91,965,961 , GRCh38.p12 chr1: 91,965,818-91,965,818 BRDT
    nsv5079839mobile element insertion1nstd203human GRCh38 chr1: 91,962,312-91,962,328 , GRCh37.p13 chr1: 92,427,869-92,427,885 BRDT
    nsv5071883mobile element insertion1nstd203human GRCh38 chr1: 91,962,167-91,962,192 , GRCh37.p13 chr1: 92,427,724-92,427,749 BRDT
    nsv5069269mobile element insertion1nstd203human GRCh38 chr1: 91,962,322-91,962,362 , GRCh37.p13 chr1: 92,427,879-92,427,919 BRDT
    nsv5067355mobile element insertion1nstd203human GRCh38 chr1: 92,005,005-92,005,018 , GRCh37.p13 chr1: 92,470,562-92,470,575 BRDT
    nsv5065983mobile element insertion1nstd203human GRCh38 chr1: 91,962,309-91,962,322 , GRCh37.p13 chr1: 92,427,866-92,427,879 BRDT
    nsv5065386mobile element insertion1nstd203human GRCh38 chr1: 91,982,735-91,982,750 , GRCh37.p13 chr1: 92,448,292-92,448,307 BRDT
    nsv5064462mobile element insertion1nstd203human GRCh38 chr1: 91,987,588-91,987,603 , GRCh37.p13 chr1: 92,453,145-92,453,160 BRDT
    nsv5063065mobile element insertion1nstd203human GRCh38 chr1: 91,962,313-91,962,322 , GRCh37.p13 chr1: 92,427,870-92,427,879 BRDT
    nsv4903766copy number variation1nstd200human GRCh38 chr1: 91,878,631-92,090,814 , GRCh37.p13 chr1: 92,344,188-92,556,371 LPCAT2BP, BRDT, 4 more genes
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