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Items: 1 to 20 of 364

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6121586copy number variation1nstd186human GRCh37 chr12: 69,871,216-69,871,674 , GRCh38.p12 chr12: 69,477,436-69,477,894 FRS2
    nsv6112755copy number variation1nstd102humanPathogenic GRCh37 chr12: 65,251,705-75,263,379 , GRCh38.p12 chr12: 64,857,925-74,869,599 LINC02421, TBC1D15, 144 more genes
    nsv5940095copy number variation1nstd209human GRCh38 chr12: 69,488,557-69,494,678 , GRCh37.p13 chr12: 69,882,337-69,888,458 FRS2
    nsv5939022copy number variation1nstd209human GRCh38 chr12: 69,484,338-69,494,718 , GRCh37.p13 chr12: 69,878,118-69,888,498 FRS2
    nsv5934529copy number variation1nstd209human GRCh38 chr12: 69,483,547-69,483,622 , GRCh37.p13 chr12: 69,877,327-69,877,402 FRS2
    nsv5930688copy number variation1nstd209human GRCh38 chr12: 69,549,013-69,552,462 , GRCh37.p13 chr12: 69,942,793-69,946,242 FRS2
    nsv5862635copy number variation1nstd209human GRCh38 chr12: 69,490,507-69,494,756 , GRCh37.p13 chr12: 69,884,287-69,888,536 FRS2
    nsv5857540copy number variation1nstd209human GRCh38 chr12: 69,549,058-69,552,698 , GRCh37.p13 chr12: 69,942,838-69,946,478 FRS2
    nsv5852063copy number variation2nstd209human GRCh38 chr12: 69,493,657-69,494,756 , GRCh37.p13 chr12: 69,887,437-69,888,536 FRS2
    nsv5730735mobile element insertion1nstd211human GRCh38 chr12: 69,509,178-69,509,178 , GRCh37.p13 chr12: 69,902,958-69,902,958 FRS2
    nsv5604411copy number variation1nstd207human GRCh38 chr12: 69,477,436-69,477,893 , GRCh37.p13 chr12: 69,871,216-69,871,673 FRS2
    nsv5561907mobile element insertion1nstd206human GRCh38 chr12: 69,509,178-69,509,229 , GRCh37.p13 chr12: 69,902,958-69,903,009 FRS2
    nsv5504157copy number variation1nstd206human GRCh38 chr12: 69,483,550-69,483,623 , GRCh37.p13 chr12: 69,877,330-69,877,403 FRS2
    nsv5501647copy number variation1nstd206human GRCh38 chr12: 69,539,940-69,545,690 , GRCh37.p13 chr12: 69,933,720-69,939,470 FRS2
    nsv5501590copy number variation1nstd206human GRCh38 chr12: 69,477,436-69,477,894 , GRCh37.p13 chr12: 69,871,216-69,871,674 FRS2
    nsv5356063translocation1nstd200human GRCh38 chr12: 69,519,387-69,519,387 , GRCh38 chr12: 69,519,475-69,519,475 , GRCh37.p13 chr12: 69,913,255-69,913,255 , GRCh37.p13 chr12: 69,913,167-69,913,167 FRS2
    nsv5356062translocation1nstd200human GRCh38 chr12: 69,483,550-69,483,550 , GRCh38 chr12: 69,483,623-69,483,623 , GRCh37.p13 chr12: 69,877,330-69,877,330 , GRCh37.p13 chr12: 69,877,403-69,877,403 FRS2
    nsv5317371copy number variation1nstd204human GRCh38.p13 chr12: 69,477,428-69,477,907 , GRCh37.p13 chr12: 69,871,208-69,871,687 FRS2
    nsv5316456copy number variation1nstd204human GRCh38.p13 chr12: 69,557,601-69,557,996 , GRCh37.p13 chr12: 69,951,381-69,951,776 FRS2
    nsv5315262copy number variation1nstd204human GRCh38.p13 chr12: 69,516,287-69,521,713 , GRCh37.p13 chr12: 69,910,067-69,915,493 FRS2
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