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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099020copy number variation1nstd102humanLikely pathogenic GRCh38 chr12: 32,843,315-32,868,927 , GRCh37.p13 chr12: 32,996,249-33,021,861 PKP2, RPL35AP27
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7098793copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 32,993,961-33,003,908 , GRCh38 chr12: 32,841,027-32,850,974 PKP2
    nsv7094044copy number variation1nstd102humanUncertain significance GRCh37 chr12: 33,021,841-33,049,665 , GRCh38.p12 chr12: 32,868,907-32,896,731 PKP2
    nsv7094043copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 32,975,391-32,977,106 , GRCh38.p12 chr12: 32,822,457-32,824,172 PKP2
    nsv7094042copy number variation1nstd102humanPathogenic GRCh37 chr12: 32,949,023-32,955,510 , GRCh38.p12 chr12: 32,796,089-32,802,576 PKP2
    nsv7094041copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 32,949,023-32,949,252 , GRCh38.p12 chr12: 32,796,089-32,796,318 PKP2
    nsv7094040copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 32,945,558-32,949,252 , GRCh38.p12 chr12: 32,792,624-32,796,318 PKP2
    nsv7073306inversion1nstd229human GRCh38 chr12: 32,891,918-32,931,987 , GRCh37.p13 chr12: 33,044,852-33,084,921 PKP2
    nsv7066078inversion1nstd229human GRCh38 chr12: 32,761,089-32,830,878 , GRCh37.p13 chr12: 32,914,023-32,983,812 PKP2
    nsv7061155inversion1nstd229human GRCh38 chr12: 32,811,473-32,846,820 , GRCh37.p13 chr12: 32,964,407-32,999,754 PKP2
    nsv6938086copy number variation1nstd229human GRCh38 chr12: 32,890,569-32,897,499 , GRCh37.p13 chr12: 33,043,503-33,050,433 PKP2
    nsv6938046copy number variation1nstd229human GRCh38 chr12: 32,869,106-32,869,284 , GRCh37.p13 chr12: 33,022,040-33,022,218 PKP2
    nsv6937850copy number variation1nstd229human GRCh38 chr12: 32,803,986-32,804,033 , GRCh37.p13 chr12: 32,956,920-32,956,967 PKP2
    nsv6936662copy number variation1nstd229human GRCh38 chr12: 32,870,519-32,876,167 , GRCh37.p13 chr12: 33,023,453-33,029,101 PKP2
    nsv6936610copy number variation1nstd229human GRCh38 chr12: 32,856,511-32,934,243 , GRCh37.p13 chr12: 33,009,445-33,087,177 PKP2, RPL35AP27
    nsv6935899copy number variation1nstd229human GRCh38 chr12: 32,803,265-32,806,424 , GRCh37.p13 chr12: 32,956,199-32,959,358 PKP2
    nsv6931430copy number variation1nstd229human GRCh38 chr12: 32,788,876-32,788,909 , GRCh37.p13 chr12: 32,941,810-32,941,843 PKP2
    nsv6930078copy number variation1nstd229human GRCh38 chr12: 32,803,069-32,816,723 , GRCh37.p13 chr12: 32,956,003-32,969,657 PKP2
    nsv6927511copy number variation1nstd229human GRCh38 chr12: 32,861,681-32,869,347 , GRCh37.p13 chr12: 33,014,615-33,022,281 PKP2, RPL35AP27
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