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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965518insertion1nstd209human GRCh38 chr1: 173,985,417-173,985,417 , GRCh37.p13 chr1: 173,954,555-173,954,555 RC3H1
    nsv5881827copy number variation1nstd209human GRCh38 chr1: 174,003,125-174,007,126 , GRCh37.p13 chr1: 173,972,263-173,976,264 RC3H1
    nsv5879382copy number variation1nstd209human GRCh38 chr1: 173,975,599-173,975,928 , GRCh37.p13 chr1: 173,944,737-173,945,066 RC3H1
    nsv5873036copy number variation1nstd209human GRCh38 chr1: 174,008,953-174,013,541 , GRCh37.p13 chr1: 173,978,091-173,982,679 RC3H1
    nsv5871345copy number variation1nstd209human GRCh38 chr1: 173,994,208-173,998,957 , GRCh37.p13 chr1: 173,963,346-173,968,095 RC3H1
    nsv5828737copy number variation1nstd209human GRCh38 chr1: 173,994,182-173,998,981 , GRCh37.p13 chr1: 173,963,320-173,968,119 RC3H1
    nsv5828549copy number variation1nstd209human GRCh38 chr1: 174,009,089-174,012,488 , GRCh37.p13 chr1: 173,978,227-173,981,626 RC3H1
    nsv5828548copy number variation1nstd209human GRCh38 chr1: 174,004,136-174,007,166 , GRCh37.p13 chr1: 173,973,274-173,976,304 RC3H1
    nsv5675020mobile element insertion1nstd211human GRCh38 chr1: 173,932,415-173,932,415 , GRCh37.p13 chr1: 173,901,553-173,901,553 RC3H1
    nsv5575386copy number variation1nstd207human GRCh38 chr1: 173,975,599-173,975,928 , GRCh37.p13 chr1: 173,944,737-173,945,066 RC3H1
    nsv5561122sequence alteration1nstd206human GRCh38 chr1: 173,979,223-173,979,925 , GRCh37.p13 chr1: 173,948,361-173,949,063 RC3H1
    nsv5542599insertion1nstd206human GRCh38 chr1: 173,979,918-173,979,918 , GRCh37.p13 chr1: 173,949,056-173,949,056 RC3H1
    nsv5429739copy number variation1nstd206human GRCh38 chr1: 173,994,211-173,998,958 , GRCh37.p13 chr1: 173,963,349-173,968,096 RC3H1
    nsv5428574copy number variation1nstd206human GRCh38 chr1: 173,989,844-173,990,720 , GRCh37.p13 chr1: 173,958,982-173,959,858 RC3H1
    nsv5420153copy number variation1nstd206human GRCh38 chr1: 173,975,617-173,975,929 , GRCh37.p13 chr1: 173,944,755-173,945,067 RC3H1
    nsv5418964copy number variation1nstd206human GRCh38 chr1: 174,008,933-174,013,564 , GRCh37.p13 chr1: 173,978,071-173,982,702 RC3H1
    nsv5417107copy number variation1nstd206human GRCh38 chr1: 174,003,102-174,007,172 , GRCh37.p13 chr1: 173,972,240-173,976,310 RC3H1
    nsv5410648mobile element insertion1nstd206human GRCh38 chr1: 173,932,415-173,932,440 , GRCh37.p13 chr1: 173,901,553-173,901,578 RC3H1
    nsv5382702mobile element deletion2nstd186human GRCh37 chr1: 173,944,755-173,945,067 , GRCh38.p12 chr1: 173,975,617-173,975,929 RC3H1
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
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