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Items: 1 to 20 of 253

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095062copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,556,653-89,851,392 , GRCh38.p12 chr16: 89,490,245-89,784,984 SNORD68, CHMP1A, 15 more genes
    nsv7095060copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,167,090-89,883,023 , GRCh38.p12 chr16: 89,100,682-89,816,615 VPS9D1, ZNF276, 26 more genes
    nsv7094940copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,611,036-90,106,937 , GRCh38.p12 chr16: 89,544,628-90,040,529 SPATA2L, LINC02166, 25 more genes
    nsv7094939copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,371,594-89,730,828 , GRCh38.p12 chr16: 89,305,186-89,664,420 LOC101930112, LOC101927863, 12 more genes
    nsv7094704copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,334,886-89,723,996 , GRCh38.p12 chr16: 89,268,478-89,657,588 LOC101930112, LOC101927863, 13 more genes
    nsv7094699copy number variation2nstd102humanUncertain significance GRCh37 chr16: 87,636,753-90,109,753 , GRCh38.p12 chr16: 87,603,147-90,043,345 HSALR1, LOC105371412, 87 more genes
    nsv7073763inversion1nstd229human GRCh38 chr16: 89,536,886-89,757,402 , GRCh37.p13 chr16: 89,603,294-89,823,810 SPATA33, SNORD68, 12 more genes
    nsv7068879inversion1nstd229human GRCh38 chr16: 89,563,448-89,590,395 , GRCh37.p13 chr16: 89,629,856-89,656,803 CPNE7, RPL13
    nsv6995211copy number variation1nstd229human GRCh38 chr16: 89,417,001-89,678,600 , GRCh37.p13 chr16: 89,483,409-89,745,008 LOC101927817, CPNE7, 11 more genes
    nsv6994002copy number variation1nstd229human GRCh38 chr16: 89,564,787-89,564,817 , GRCh37.p13 chr16: 89,631,195-89,631,225 RPL13
    nsv6992944copy number variation1nstd229human GRCh38 chr16: 89,301,591-89,661,186 , GRCh37.p13 chr16: 89,367,999-89,727,594 CMPK1P2, LOC101927863, 12 more genes
    nsv6985866copy number variation1nstd229human GRCh38 chr16: 89,473,541-89,719,269 , GRCh37.p13 chr16: 89,539,949-89,785,677 ANKRD11, SPATA33, 14 more genes
    nsv6634465copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 71,610,276-90,354,753 , GRCh38.p12 chr16: 71,576,373-90,228,345 AP1G1, AFG3L1P, 349 more genes
    nsv6509402copy number variation1nstd223human GRCh38 chr16: 89,544,513-89,596,810 , GRCh37.p13 chr16: 89,610,921-89,663,218 SPG7, SNORD68, 2 more genes
    nsv6504603copy number variation1nstd223human GRCh38 chr16: 89,558,590-89,558,871 , GRCh37.p13 chr16: 89,624,998-89,625,279 RPL13
    nsv6496218copy number variation1nstd223human GRCh38 chr16: 89,346,802-89,674,039 , GRCh37.p13 chr16: 89,413,210-89,740,447 CPNE7, RNU6-430P, 11 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6291643copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,337,891-90,155,062 , GRCh38.p12 chr16: 89,271,483-90,088,654 DBNDD1, AFG3L1P, 34 more genes
    nsv6291569copy number variation1nstd102humanUncertain significance GRCh37 chr16: 88,000,389-90,155,062 , GRCh38.p12 chr16: 87,966,783-90,088,654 CTU2, CDT1, 78 more genes
    nsv6290331copy number variation1nstd102humanPathogenic GRCh37 chr16: 80,386,595-90,163,348 , GRCh38.p12 chr16: 80,352,698-90,096,940 GINS2, TCF25, 220 more genes
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