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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5948463insertion1nstd209human GRCh38 chr10: 30,325,833-30,325,833 , GRCh37.p13 chr10: 30,614,762-30,614,762 MTPAP
    nsv5914382copy number variation1nstd209human GRCh38 chr10: 27,312,316-36,846,398 , GRCh37.p13 chr10: 27,601,245-37,135,326 , RN7SL241P, 160 more genes
    nsv5711719mobile element insertion2nstd211human GRCh38 chr10: 30,325,849-30,325,849 , GRCh37.p13 chr10: 30,614,778-30,614,778 MTPAP
    nsv5625184insertion1nstd207human GRCh38 chr10: 30,325,833-30,325,833 , GRCh37.p13 chr10: 30,614,762-30,614,762 MTPAP
    nsv5550023insertion1nstd206human GRCh38 chr10: 30,317,511-30,317,561 , GRCh37.p13 chr10: 30,606,440-30,606,490 MTPAP
    nsv5490436copy number variation1nstd206human GRCh38 chr10: 30,333,081-30,335,936 , GRCh37.p13 chr10: 30,622,010-30,624,865 MTPAP
    nsv5487712copy number variation1nstd206human GRCh38 chr10: 30,349,785-30,350,719 , GRCh37.p13 chr10: 30,638,714-30,639,648 MTPAP
    nsv5486867copy number variation1nstd206human GRCh38 chr10: 30,323,395-30,324,114 , GRCh37.p13 chr10: 30,612,324-30,613,043 MTPAP
    nsv5397522mobile element insertion1nstd206human GRCh38 chr10: 30,325,833-30,325,833 , GRCh37.p13 chr10: 30,614,762-30,614,762 MTPAP
    nsv5246248copy number variation1nstd204human GRCh38.p13 chr10: 30,325,491-30,326,523 , GRCh37.p13 chr10: 30,614,420-30,615,452 MTPAP
    nsv5139628mobile element insertion1nstd203human GRCh38 chr10: 30,325,838-30,325,849 , GRCh37.p13 chr10: 30,614,767-30,614,778 MTPAP
    nsv5138971mobile element insertion1nstd203human GRCh38 chr10: 30,325,836-30,325,849 , GRCh37.p13 chr10: 30,614,765-30,614,778 MTPAP
    nsv5133434mobile element insertion1nstd203human GRCh38 chr10: 30,338,056-30,338,085 , GRCh37.p13 chr10: 30,626,985-30,627,014 MTPAP
    nsv5131038mobile element insertion1nstd203human GRCh38 chr10: 30,338,289-30,338,289 , GRCh37.p13 chr10: 30,627,218-30,627,218 MTPAP
    nsv5126904mobile element insertion1nstd203human GRCh38 chr10: 30,325,840-30,325,849 , GRCh37.p13 chr10: 30,614,769-30,614,778 MTPAP
    nsv5124417mobile element insertion1nstd203human GRCh38 chr10: 30,325,832-30,325,849 , GRCh37.p13 chr10: 30,614,761-30,614,778 MTPAP
    nsv5120667mobile element insertion1nstd203human GRCh38 chr10: 30,325,833-30,325,849 , GRCh37.p13 chr10: 30,614,762-30,614,778 MTPAP
    nsv4988714copy number variation1nstd200human GRCh38 chr10: 30,056,047-30,401,336 , GRCh37.p13 chr10: 30,344,976-30,690,265 DNM1P17, MIR7162, 11 more genes
    nsv4975648copy number variation1nstd200human GRCh38 chr10: 30,316,979-30,318,340 , GRCh37.p13 chr10: 30,605,908-30,607,269 MTPAP
    nsv4846314copy number variation1nstd200human GRCh37 chr10: 30,616,268-30,617,973 , GRCh38.p12 chr10: 30,327,339-30,329,044 MTPAP
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