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Items: 1 to 20 of 306

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112722copy number variation1nstd102humanPathogenic GRCh37 chrX: 42,069,104-45,843,277 , GRCh38.p12 chrX: 42,209,851-45,983,842 TATDN2P1, RRM2P3, 36 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5976000copy number variation1nstd209human GRCh38 chrX: 43,948,881-43,965,684 , GRCh37.p13 chrX: 43,808,127-43,824,930 NDP, NDP-AS1
    nsv5873682copy number variation1nstd209human GRCh38 chrX: 41,560,623-47,265,899 , GRCh37.p13 chrX: 41,419,876-47,125,298 , CTNNBL1P1, 80 more genes
    nsv5423676copy number variation1nstd206human GRCh38 chrX: 43,964,271-43,964,353 , GRCh37.p13 chrX: 43,823,517-43,823,599 NDP-AS1, NDP
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5381750copy number variation1nstd102humanUncertain significance GRCh37 chrX: 43,809,045-43,817,891 , GRCh38.p12 chrX: 43,949,799-43,958,645 NDP, NDP-AS1
    nsv5381749copy number variation1nstd102humanPathogenic GRCh37 chrX: 39,645,568-44,199,000 , GRCh38.p12 chrX: 39,786,314-44,339,754 EFHC2, GPR82, 58 more genes
    nsv5381697copy number variation1nstd102humanPathogenic GRCh37 chrX: 41,342,834-43,901,936 , GRCh38.p12 chrX: 41,483,581-44,042,690 GPR82, RNU6-1124P, 22 more genes
    nsv5376156translocation1nstd200human GRCh38 chrX: 43,964,271-43,964,271 , GRCh38 chrX: 43,964,353-43,964,353 , GRCh37.p13 chrX: 43,823,599-43,823,599 , GRCh37.p13 chrX: 43,823,517-43,823,517 NDP-AS1, NDP
    nsv5330060translocation1nstd200human GRCh37 chrX: 43,816,833-43,816,833 , GRCh37 chrX: 43,817,260-43,817,260 , GRCh38.p12 chrX: 43,957,587-43,957,587 , GRCh38.p12 chrX: 43,958,014-43,958,014 NDP, NDP-AS1
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4905438copy number variation1nstd200human GRCh38 chrX: 43,818,631-43,951,183 , GRCh37.p13 chrX: 43,677,878-43,810,429 NDP-AS1, MAOB, 1 more genes
    nsv4771319copy number variation1nstd200human GRCh37 chrX: 43,823,517-43,823,599 , GRCh38.p12 chrX: 43,964,271-43,964,353 NDP, NDP-AS1
    nsv4728486copy number variation1nstd102humanPathogenic GRCh37 chrX: 219,609-55,466,476 , GRCh38.p12 chrX: 302,942-55,440,043 CDK16, WASF4P, 772 more genes
    nsv4728434copy number variation1nstd102humanUncertain significance GRCh37 chrX: 43,740,441-43,858,706 , GRCh38.p12 chrX: 43,881,195-43,999,460 NDP, NDP-AS1, 1 more genes
    nsv4685953copy number variation1nstd102humanPathogenic GRCh37 chrX: 41,150,139-43,976,458 , GRCh38.p12 chrX: 41,290,886-44,117,212 GEMIN7P1, PINCR, 28 more genes
    nsv4684016inversion1nstd191human GRCh37.p13 chrX: 32,933,886-87,244,324 , GRCh38 chrX: 32,915,769-87,989,324 , ABCB7, 816 more genes
    nsv4674588copy number variation1nstd102humanPathogenic GRCh37 chrX: 539,722-55,509,385 , GRCh38.p12 chrX: 578,987-55,482,952 LOC392440, SSX4, 769 more genes
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