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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137115copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,467,726-29,044,717 , GRCh38.p12 chr16: 21,456,405-29,033,396 OTOAP1, GGA2, 148 more genes
    nsv6992078copy number variation1nstd229human GRCh38 chr16: 26,975,134-27,204,892 , GRCh37.p13 chr16: 26,986,455-27,216,213 KDM8, LOC105371154, 4 more genes
    nsv6990562copy number variation1nstd229human GRCh38 chr16: 27,222,157-27,225,267 , GRCh37.p13 chr16: 27,233,478-27,236,588 KDM8, NSMCE1
    nsv6984493copy number variation1nstd229human GRCh38 chr16: 26,445,367-27,411,745 , GRCh37.p13 chr16: 26,456,688-27,423,066 LOC105371153, KDM8, 9 more genes
    nsv6981784copy number variation1nstd229human GRCh38 chr16: 27,185,024-27,226,724 , GRCh37.p13 chr16: 27,196,345-27,238,045 KDM8, NSMCE1
    nsv6637633copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,576,803-30,177,240 , GRCh38.p12 chr16: 21,565,482-30,165,919 USP31, CA5AP1, 200 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    nsv6499029copy number variation1nstd223human GRCh38 chr16: 27,222,157-27,225,258 , GRCh37.p13 chr16: 27,233,478-27,236,579 NSMCE1, KDM8
    nsv6498423copy number variation1nstd223human GRCh38 chr16: 27,185,024-27,226,722 , GRCh37.p13 chr16: 27,196,345-27,238,043 KDM8, NSMCE1
    nsv6290289copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,594,997-29,625,302 , GRCh38.p12 chr16: 21,583,676-29,613,981 LOC105371149, SLX1B, 166 more genes
    nsv6289847copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,530,207-29,332,245 , GRCh38.p12 chr16: 21,518,886-29,320,924 GAPDHP35, NSMCE1, 154 more genes
    nsv6133268copy number variation1nstd213human GRCh37 chr16: 22,710,000-32,010,001 , GRCh38.p12 chr16: 22,698,679-31,998,680 ALDOA, AQP8, 269 more genes
    nsv6133267copy number variation1nstd213human GRCh37 chr16: 22,710,000-30,200,001 , GRCh38.p12 chr16: 22,698,679-30,188,680 ALDOA, AQP8, 169 more genes
    nsv5940135copy number variation1nstd209human GRCh38 chr16: 27,205,658-27,207,227 , GRCh37.p13 chr16: 27,216,979-27,218,548 KDM8
    nsv5530262copy number variation1nstd206human GRCh38 chr16: 27,215,152-27,215,279 , GRCh37.p13 chr16: 27,226,473-27,226,600 KDM8
    nsv5523610copy number variation1nstd206human GRCh38 chr16: 27,201,257-27,316,154 , GRCh37.p13 chr16: 27,212,578-27,327,475 IL4R, NSMCE1, 2 more genes
    nsv5003353copy number variation1nstd200human GRCh38 chr16: 27,222,157-27,225,258 , GRCh37.p13 chr16: 27,233,478-27,236,579 KDM8, NSMCE1
    nsv4864080copy number variation1nstd200human GRCh37 chr16: 26,413,712-27,385,346 , GRCh38.p12 chr16: 26,402,391-27,374,025 KDM8, EEF1A1P38, 8 more genes
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 NPIPB9, TMEM219, 597 more genes
    nsv4729822copy number variation1nstd102humanUncertain significance GRCh37 chr16: 26,457,597-27,420,153 , GRCh38.p12 chr16: 26,446,276-27,408,832 LINC02195, LOC105371155, 9 more genes
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