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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048441inversion1nstd229human GRCh38 chr3: 148,697,295-148,703,974 , GRCh37.p13 chr3: 148,415,082-148,421,761 AGTR1
    nsv6734550copy number variation1nstd229human GRCh38 chr3: 148,212,198-148,778,023 , GRCh37.p13 chr3: 147,929,985-148,495,810 AGTR1, LOC105374147, 5 more genes
    nsv6721378copy number variation1nstd229human GRCh38 chr3: 148,715,781-148,718,631 , GRCh37.p13 chr3: 148,433,568-148,436,418 AGTR1
    nsv6721268copy number variation1nstd229human GRCh38 chr3: 148,718,846-148,723,919 , GRCh37.p13 chr3: 148,436,633-148,441,706 AGTR1
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6372973copy number variation1nstd223human GRCh38 chr3: 148,695,001-148,699,800 , GRCh37.p13 chr3: 148,412,788-148,417,587 RPL38P1, AGTR1
    nsv6357095copy number variation1nstd223human GRCh38 chr3: 148,717,478-148,718,122 , GRCh37.p13 chr3: 148,435,265-148,435,909 AGTR1
    nsv6313678copy number variation1nstd102humanPathogenic GRCh37 chr3: 145,486,960-160,504,834 , GRCh38.p12 chr3: 145,769,173-160,787,046 RNU6-901P, RPL32P8, 229 more genes
    nsv6311444copy number variation1nstd102humanPathogenic GRCh37 chr3: 148,447,967-151,176,497 , GRCh38.p12 chr3: 148,730,180-151,458,709 TM4SF1, FKBP1AP4, 68 more genes
    nsv6290273copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,729,607-157,921,084 , GRCh38.p12 chr3: 143,010,765-158,203,295 LINC02066, TM4SF1-AS1, 206 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 LOC102724145, C3orf80, 273 more genes
    nsv6262863copy number variation1nstd214human GRCh38 chr3: 148,696,802-148,696,915 , GRCh37.p13 chr3: 148,414,589-148,414,702 AGTR1
    nsv6259785mobile element insertion1nstd215human GRCh38 chr3: 148,715,276-148,715,276 , GRCh37.p13 chr3: 148,433,063-148,433,063 AGTR1
    nsv6134997copy number variation1nstd213human GRCh37 chr3: 148,320,000-148,590,001 , GRCh38.p12 chr3: 148,602,213-148,872,214 AGTR1, CPA3, 3 more genes
    nsv6134994copy number variation1nstd213human GRCh37 chr3: 139,490,000-150,360,001 , GRCh38.p12 chr3: 139,771,158-150,642,214 , ATP1B3, 147 more genes
    nsv5694189mobile element insertion2nstd211human GRCh38 chr3: 148,715,276-148,715,276 , GRCh37.p13 chr3: 148,433,063-148,433,063 AGTR1
    nsv5676766mobile element insertion1nstd211human GRCh38 chr3: 148,726,650-148,726,650 , GRCh37.p13 chr3: 148,444,437-148,444,437 AGTR1
    nsv5437560copy number variation1nstd206human GRCh38 chr3: 148,696,328-148,696,546 , GRCh37.p13 chr3: 148,414,115-148,414,333 RPL38P1, AGTR1
    nsv5411034mobile element insertion1nstd206human GRCh38 chr3: 148,715,276-148,715,327 , GRCh37.p13 chr3: 148,433,063-148,433,114 AGTR1
    nsv5410348mobile element insertion1nstd206human GRCh38 chr3: 148,726,650-148,726,701 , GRCh37.p13 chr3: 148,444,437-148,444,488 AGTR1
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