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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3917670copy number variation1nstd102humanUncertain significance NCBI36 chr16: 28,045,350-28,285,087 , GRCh37.p13 chr16: 28,137,849-28,377,586 , GRCh38.p12 chr16: 28,126,528-28,366,265 XPO6, NPIPB6, 3 more genes
    nsv3919862copy number variation1nstd102humanUncertain significance NCBI36 chr16: 28,045,350-28,246,173 , GRCh37.p13 chr16: 28,137,849-28,338,672 , GRCh38.p12 chr16: 28,126,528-28,327,351 XPO6, SBK1, 2 more genes
    nsv3905855copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,596,299-30,399,167 , GRCh38.p12 chr16: 21,584,978-30,387,846 XPO6, LOC107984874, 217 more genes
    nsv6290289copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,594,997-29,625,302 , GRCh38.p12 chr16: 21,583,676-29,613,981 XPO6, LOC105371149, 166 more genes
    nsv3891271copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,379,628-29,379,768 , GRCh38.p12 chr16: 21,368,307-29,368,447 XPO6, LOC101927814, 159 more genes
    nsv6289847copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,530,207-29,332,245 , GRCh38.p12 chr16: 21,518,886-29,320,924 XPO6, GAPDHP35, 154 more genes
    nsv7137115copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,467,726-29,044,717 , GRCh38.p12 chr16: 21,456,405-29,033,396 XPO6, OTOAP1, 148 more genes
    nsv3924349copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,612,313-28,334,665 , GRCh38 chr16: 21,600,992-28,323,344 , NCBI36 chr16: 21,519,814-28,242,166 XPO6, SLC5A11, 111 more genes
    nsv7094777copy number variation1nstd102humanPathogenic GRCh37 chr16: 27,441,393-29,001,333 , GRCh38.p12 chr16: 27,430,072-28,990,012 XPO6, NUPR1, 45 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 XPO6, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 XPO6, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 XPO6, LINC02175, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 XPO6, PRSS53, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 XPO6, FTLP14, 1868 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 XPO6, LOC105371069, 654 more genes
    nsv1398297copy number variation1nstd102humanPathogenic GRCh37 chr16: 102,839-28,327,676 , GRCh38.p12 chr16: 52,839-28,316,355 XPO6, BMERB1, 701 more genes
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 XPO6, NPIPB9, 597 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 XPO6, MIR6511B2, 535 more genes
    nsv3910441copy number variation1nstd102humanPathogenic NCBI36 chr16: 4,634,894-29,089,642 , GRCh37 chr16: 4,694,893-29,182,141 , GRCh38 chr16: 4,644,892-29,170,820 XPO6, LOC729945, 450 more genes
    nsv3917409copy number variation1nstd102humanPathogenic NCBI36 chr16: 14,956,252-28,225,665 , GRCh37 chr16: 15,048,751-28,318,164 , GRCh38 chr16: 14,954,894-28,306,843 XPO6, SLC7A5P2, 251 more genes
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