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Items: 1 to 20 of 27

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3907258copy number variation1nstd102humanBenign GRCh37 chr16: 11,762,023-11,764,677 , GRCh38.p12 chr16: 11,668,167-11,670,821 SNN
    nsv3909516copy number variation1nstd102humanBenign GRCh37 chr16: 11,762,100-11,762,770 , GRCh38.p12 chr16: 11,668,244-11,668,914 SNN
    nsv3898358copy number variation1nstd102humanBenign GRCh37 chr16: 11,762,200-11,762,770 , GRCh38.p12 chr16: 11,668,344-11,668,914 SNN
    nsv3899422copy number variation1nstd102humanBenign GRCh37 chr16: 11,762,200-11,762,756 , GRCh38.p12 chr16: 11,668,344-11,668,900 SNN
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 SNN, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 SNN, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 SNN, LINC02175, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 SNN, PRSS53, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 SNN, FTLP14, 1868 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 SNN, LOC105371069, 654 more genes
    nsv1398297copy number variation1nstd102humanPathogenic GRCh37 chr16: 102,839-28,327,676 , GRCh38.p12 chr16: 52,839-28,316,355 SNN, BMERB1, 701 more genes
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 SNN, NPIPB9, 597 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 SNN, 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 SNN, LOC729945, 450 more genes
    nsv3903116copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-22,442,007 , GRCh38.p12 chr16: 35,880-22,430,686 SNN, NPIPA8, 616 more genes
    nsv3900978copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-19,806,921 , GRCh38.p12 chr16: 35,880-19,795,599 SNN, LOC105371091, 543 more genes
    nsv3915829copy number variation1nstd102humanPathogenic NCBI36 chr16: 656,663-15,744,462 , GRCh38 chr16: 666,662-15,743,104 , GRCh37 chr16: 716,662-15,836,961 SNN, RPL35AP34, 429 more genes
    nsv3923267copy number variation1nstd102humanPathogenic GRCh37 chr16: 93,732-13,420,663 , GRCh38 chr16: 43,732-13,326,806 , NCBI36 chr16: 33,732-13,328,164 SNN, METRN, 413 more genes
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 SNN, ABAT, 876 more genes
    nsv3886214copy number variation1nstd102humanLikely pathogenic GRCh38 chr16: 11,369,400-13,577,493 , GRCh37.p13 chr16: 11,463,257-13,671,350 SNN, TNFRSF17, 30 more genes
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