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Items: 1 to 20 of 452

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970372inversion1nstd209human GRCh38 chr1: 25,350,900-25,370,016 , GRCh37.p13 chr1: 25,677,391-25,696,507 RHCE, TMEM50A
    nsv5873119copy number variation1nstd209human GRCh38 chr1: 25,376,348-25,379,174 , GRCh37.p13 chr1: 25,702,839-25,705,665 RHCE
    nsv5870847copy number variation1nstd209human GRCh38 chr1: 25,287,187-25,405,613 , GRCh37.p13 chr1: 25,613,678-25,732,104 RHCE, RHD, 4 more genes
    nsv5829961copy number variation1nstd209human GRCh38 chr1: 25,409,658-25,411,225 , GRCh37.p13 chr1: 25,736,149-25,737,716 RHCE
    nsv5829960copy number variation2nstd209human GRCh38 chr1: 25,399,589-25,405,301 , GRCh37.p13 chr1: 25,726,080-25,731,792 SDHDP7, RHCE
    nsv5829959copy number variation2nstd209human GRCh38 chr1: 25,398,687-25,400,665 , GRCh37.p13 chr1: 25,725,178-25,727,156 SDHDP7, RHCE
    nsv5829958copy number variation1nstd209human GRCh38 chr1: 25,350,231-25,360,357 , GRCh37.p13 chr1: 25,676,722-25,686,848 RHCE, TMEM50A
    nsv5829926copy number variation1nstd209human GRCh38 chr1: 25,414,042-25,416,918 , GRCh37.p13 chr1: 25,740,533-25,743,409 RHCE
    nsv5829925copy number variation2nstd209human GRCh38 chr1: 25,405,603-25,409,326 , GRCh37.p13 chr1: 25,732,094-25,735,817 RHCE
    nsv5829924copy number variation2nstd209human GRCh38 chr1: 25,375,741-25,377,269 , GRCh37.p13 chr1: 25,702,232-25,703,760 RHCE
    nsv5829805copy number variation2nstd209human GRCh38 chr1: 25,400,966-25,404,100 , GRCh37.p13 chr1: 25,727,457-25,730,591 RHCE
    nsv5829804copy number variation2nstd209human GRCh38 chr1: 25,381,354-25,393,334 , GRCh37.p13 chr1: 25,707,845-25,719,825 RHCE
    nsv5829803copy number variation2nstd209human GRCh38 chr1: 25,367,669-25,375,352 , GRCh37.p13 chr1: 25,694,160-25,701,843 RHCE
    nsv5829660copy number variation1nstd209human GRCh38 chr1: 25,405,602-25,407,967 , GRCh37.p13 chr1: 25,732,093-25,734,458 RHCE
    nsv5829659copy number variation2nstd209human GRCh38 chr1: 25,402,530-25,404,895 , GRCh37.p13 chr1: 25,729,021-25,731,386 RHCE
    nsv5829658copy number variation2nstd209human GRCh38 chr1: 25,374,215-25,381,253 , GRCh37.p13 chr1: 25,700,706-25,707,744 RHCE
    nsv5721982mobile element insertion1nstd211human GRCh38 chr1: 25,359,547-25,359,547 , GRCh37.p13 chr1: 25,686,038-25,686,038 TMEM50A, RHCE
    nsv5693028mobile element insertion1nstd211human GRCh38 chr1: 25,429,243-25,429,243 , GRCh37.p13 chr1: 25,755,734-25,755,734 RHCE, MACO1
    nsv5669492inversion1nstd207human GRCh38 chr1: 25,338,356-25,362,421 , GRCh37.p13 chr1: 25,664,847-25,688,912 RHCE, TMEM50A, 1 more genes
    nsv5622340insertion1nstd207human GRCh38 chr1: 25,405,607-25,405,607 , GRCh37.p13 chr1: 25,732,098-25,732,098 RHCE
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