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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5620536insertion1nstd207human GRCh38 chr1: 41,369,871-41,369,871 , GRCh37.p13 chr1: 41,835,543-41,835,543 FOXO6
    nsv5611623insertion1nstd207human GRCh38 chr1: 41,382,200-41,382,200 , GRCh37.p13 chr1: 41,847,872-41,847,872 FOXO6
    nsv5550951insertion1nstd206human GRCh38 chr1: 41,369,873-41,369,922 , GRCh37.p13 chr1: 41,835,545-41,835,594 FOXO6
    nsv5294491copy number variation1nstd204human GRCh38.p13 chr1: 41,382,467-41,382,629 , GRCh37.p13 chr1: 41,848,139-41,848,301 FOXO6
    nsv5068719mobile element insertion1nstd203human GRCh38 chr1: 41,361,216-41,361,216 , GRCh37.p13 chr1: 41,826,888-41,826,888 FOXO6
    nsv4906132copy number variation1nstd200human GRCh38 chr1: 41,373,447-41,375,347 , GRCh37.p13 chr1: 41,839,119-41,841,019 FOXO6-AS1, FOXO6
    nsv4773232copy number variation1nstd200human GRCh37 chr1: 41,839,119-41,841,019 , GRCh38.p12 chr1|NW_009646194.1: 123,176-125,076 , GRCh38.p12 chr1: 41,373,447-41,375,347 FOXO6, FOXO6-AS1
    nsv4768901insertion1nstd186human GRCh37 chr1: 41,847,873-41,847,873 , GRCh38.p12 chr1: 41,382,201-41,382,201 , GRCh38.p12 chr1|NW_009646194.1: 131,897-131,897 FOXO6
    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
    nsv4758273insertion1nstd199human GRCh37 chr1: 41,835,541-41,835,541 , GRCh38.p12 chr1|NW_009646194.1: 119,544-119,544 , GRCh38.p12 chr1: 41,369,869-41,369,869 FOXO6
    nsv4756327insertion1nstd199human GRCh37 chr1: 41,847,872-41,847,872 , GRCh38.p12 chr1|NW_009646194.1: 131,896-131,896 , GRCh38.p12 chr1: 41,382,200-41,382,200 FOXO6
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4684700insertion1nstd194human GRCh37 chr1: 41,847,873-41,847,873 , GRCh38.p12 chr1: 41,382,201-41,382,201 , GRCh38.p12 chr1|NW_009646194.1: 131,897-131,897 FOXO6
    nsv4445312insertion1nstd175human GRCh37 chr1: 41,835,543-41,835,543 , GRCh38.p12 chr1: 41,369,871-41,369,871 , GRCh38.p12 chr1|NW_009646194.1: 119,546-119,546 FOXO6
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 LINC01776, IGSF21-AS1, 1853 more genes
    nsv4326932inversion1nstd166human GRCh37.p13 chr1: 35,173,490-93,458,530 , GRCh38.p12 chr1: 34,707,889-92,992,973 , ATP6V0B, 1069 more genes
    nsv3947929insertion1nstd167human GRCh37 chr1: 41,847,872-41,847,872 , GRCh38.p12 chr1: 41,382,200-41,382,200 , GRCh38.p12 chr1|NW_009646194.1: 131,896-131,896 FOXO6
    nsv3944197insertion1nstd167human GRCh37 chr1: 41,835,543-41,835,543 , GRCh38.p12 chr1: 41,369,871-41,369,871 , GRCh38.p12 chr1|NW_009646194.1: 119,546-119,546 FOXO6
    nsv3908884copy number variation1nstd102humanPathogenic GRCh37 chr1: 41,300,076-43,588,742 , GRCh38 chr1: 40,834,404-43,123,071 , NCBI36 chr1: 41,072,663-43,361,329 PPCS, ZNF691, 46 more genes
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