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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5938739copy number variation1nstd209human GRCh38 chr12: 50,469,860-50,470,071 , GRCh37.p13 chr12: 50,863,643-50,863,854 LARP4
    nsv5937667copy number variation1nstd209human GRCh38 chr12: 50,467,378-50,470,376 , GRCh37.p13 chr12: 50,861,161-50,864,159 LARP4
    nsv5850853copy number variation1nstd209human GRCh38 chr12: 50,467,568-50,470,317 , GRCh37.p13 chr12: 50,861,351-50,864,100 LARP4
    nsv5712751mobile element insertion2nstd211human GRCh38 chr12: 50,437,402-50,437,402 , GRCh37.p13 chr12: 50,831,185-50,831,185 LARP4
    nsv5701001mobile element insertion1nstd211human GRCh38 chr12: 50,408,213-50,408,213 , GRCh37.p13 chr12: 50,801,996-50,801,996 LARP4
    nsv5658729insertion1nstd207human GRCh38 chr12: 50,446,356-50,446,356 , GRCh37.p13 chr12: 50,840,139-50,840,139 LARP4
    nsv5650196insertion1nstd207human GRCh38 chr12: 50,446,374-50,446,374 , GRCh37.p13 chr12: 50,840,157-50,840,157 LARP4
    nsv5509187copy number variation1nstd206human GRCh38 chr12: 50,418,076-50,423,971 , GRCh37.p13 chr12: 50,811,859-50,817,754 LARP4
    nsv5507022copy number variation1nstd206human GRCh38 chr12: 50,467,378-50,470,377 , GRCh37.p13 chr12: 50,861,161-50,864,160 LARP4
    nsv5497704copy number variation1nstd206human GRCh38 chr12: 50,392,137-50,399,649 , GRCh37.p13 chr12: 50,785,920-50,793,432 FAM186A, LARP4
    nsv5496788copy number variation1nstd206human GRCh38 chr12: 50,455,516-50,457,238 , GRCh37.p13 chr12: 50,849,299-50,851,021 LARP4, SNORD133
    nsv5422632mobile element insertion1nstd206human GRCh38 chr12: 50,437,402-50,437,453 , GRCh37.p13 chr12: 50,831,185-50,831,236 LARP4
    nsv5138948mobile element insertion1nstd203human GRCh38 chr12: 50,449,923-50,449,952 , GRCh37.p13 chr12: 50,843,706-50,843,735 LARP4
    nsv5138621mobile element insertion1nstd203human GRCh38 chr12: 50,437,389-50,437,402 , GRCh37.p13 chr12: 50,831,172-50,831,185 LARP4
    nsv5138328mobile element insertion1nstd203human GRCh38 chr12: 50,437,392-50,437,402 , GRCh37.p13 chr12: 50,831,175-50,831,185 LARP4
    nsv5134286mobile element insertion1nstd203human GRCh38 chr12: 50,437,394-50,437,402 , GRCh37.p13 chr12: 50,831,177-50,831,185 LARP4
    nsv5132526mobile element insertion1nstd203human GRCh38 chr12: 50,437,388-50,437,402 , GRCh37.p13 chr12: 50,831,171-50,831,185 LARP4
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv4985586copy number variation1nstd200human GRCh38 chr12: 50,432,547-50,451,567 , GRCh37.p13 chr12: 50,826,330-50,845,350 LARP4
    nsv4985585copy number variation1nstd200human GRCh38 chr12: 50,418,189-50,423,685 , GRCh37.p13 chr12: 50,811,972-50,817,468 LARP4
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