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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv7068303inversion1nstd229human GRCh38 chr16: 89,906,627-89,911,425 , GRCh37.p13 chr16: 89,973,035-89,977,833 TCF25
    nsv7062628inversion1nstd229human GRCh38 chr16: 89,906,790-89,913,891 , GRCh37.p13 chr16: 89,973,198-89,980,299 TCF25
    nsv6983724copy number variation1nstd229human GRCh38 chr16: 89,879,022-89,881,749 , GRCh37.p13 chr16: 89,945,430-89,948,157 TCF25
    nsv6980013copy number variation1nstd229human GRCh38 chr16: 89,888,001-89,890,200 , GRCh37.p13 chr16: 89,954,409-89,956,608 TCF25
    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
    nsv6588750inversion1nstd223human GRCh38 chr16: 89,875,540-89,876,952 , GRCh37.p13 chr16: 89,941,948-89,943,360 TCF25
    nsv6514632copy number variation1nstd223human GRCh38 chr16: 89,886,409-89,886,710 , GRCh37.p13 chr16: 89,952,817-89,953,118 TCF25
    nsv6513305copy number variation1nstd223human GRCh38 chr16: 89,876,901-89,880,600 , GRCh37.p13 chr16: 89,943,309-89,947,008 TCF25
    nsv6510878copy number variation1nstd223human GRCh38 chr16: 89,882,266-89,882,799 , GRCh37.p13 chr16: 89,948,674-89,949,207 TCF25
    nsv6508146copy number variation1nstd223human GRCh38 chr16: 89,890,283-89,890,577 , GRCh37.p13 chr16: 89,956,691-89,956,985 TCF25
    nsv6500661copy number variation1nstd223human GRCh38 chr16: 89,839,303-90,017,373 , GRCh37.p13 chr16: 89,905,711-90,083,781 DEF8, SPIRE2, 8 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
    nsv6314206copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,763,758-89,961,958 , GRCh38.p12 chr16: 89,697,350-89,895,550 VPS9D1, ZNF276, 6 more genes
    nsv6306654copy number variation1nstd186human GRCh37 chr16: 89,974,265-89,974,332 , GRCh38.p12 chr16: 89,907,857-89,907,924 TCF25
    nsv6305856copy number variation1nstd186human GRCh37 chr16: 89,974,342-89,975,139 , GRCh38.p12 chr16: 89,907,934-89,908,731 TCF25
    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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