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Items: 1 to 20 of 243

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096530copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,130,113-10,133,956 , GRCh38.p12 chr3: 10,088,429-10,092,272 FANCD2OS, FANCD2
    nsv7096528copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,094,051-11,078,652 , GRCh38.p12 chr3: 10,052,367-11,036,966 LINC00606, MIR378B, 19 more genes
    nsv7096432copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,127,476-10,136,978 , GRCh38.p12 chr3: 10,085,792-10,095,294 FANCD2OS, FANCD2
    nsv7055847inversion1nstd229human GRCh38 chr3: 5,111,802-11,290,661 , GRCh37.p13 chr3: 5,153,487-11,332,347 GHRLOS, LHFPL4, 96 more genes
    nsv7042755inversion1nstd229human GRCh38 chr3: 8,982,205-12,221,239 , GRCh37.p13 chr3: 9,023,889-12,262,739 SYN2, MTCO1P5, 74 more genes
    nsv6716092copy number variation1nstd229human GRCh38 chr3: 10,078,920-10,248,061 , GRCh37.p13 chr3: 10,120,604-10,289,745 VHL, FANCD2OS, 4 more genes
    nsv6715869copy number variation1nstd229human GRCh38 chr3: 9,686,801-10,627,600 , GRCh37.p13 chr3: 9,728,485-10,669,285 FANCD2OS, CRELD1, 40 more genes
    nsv6708961copy number variation1nstd229human GRCh38 chr3: 10,083,101-10,103,479 , GRCh37.p13 chr3: 10,124,785-10,145,163 FANCD2, FANCD2OS
    nsv6705199copy number variation1nstd229human GRCh38 chr3: 10,101,484-10,103,581 , GRCh37.p13 chr3: 10,143,168-10,145,265 FANCD2OS, FANCD2
    nsv6702167copy number variation1nstd229human GRCh38 chr3: 10,101,483-10,106,105 , GRCh37.p13 chr3: 10,143,167-10,147,789 FANCD2OS, FANCD2
    nsv6698744copy number variation1nstd229human GRCh38 chr3: 10,083,301-10,510,500 , GRCh37.p13 chr3: 10,124,985-10,552,184 MIR885, IRAK2, 12 more genes
    nsv6637145copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,931-10,687,964 , GRCh38.p12 chr3: 19,253-10,646,279 RN7SL120P, LOC105376940, 132 more genes
    nsv6637039copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,024,917-11,917,048 , GRCh38.p12 chr3: 9,983,233-11,875,574 ATG7, GHRL, 35 more genes
    nsv6636952copy number variation1nstd102humanUncertain significance GRCh37 chr3: 9,908,803-10,265,564 , GRCh38.p12 chr3: 9,867,119-10,223,880 CIDECP1, CIDEC, 19 more genes
    nsv6636289copy number variation1nstd102humanUncertain significance GRCh37 chr3: 9,754,612-10,295,828 , GRCh38.p12 chr3: 9,712,928-10,254,144 FANCD2P1, RNU6-882P, 30 more genes
    nsv6636276copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,892-11,679,509 , GRCh38.p12 chr3: 20,214-11,638,035 RPL23AP39, LOC107986059, 144 more genes
    nsv6628615copy number variation1nstd224human GRCh37 chr3: 10,134,996-10,219,689 , GRCh38.p12 chr3: 10,093,312-10,178,005 BRK1, FANCD2OS, 3 more genes
    nsv6554571inversion1nstd223human GRCh38 chr3: 10,100,379-10,101,069 , GRCh37.p13 chr3: 10,142,063-10,142,753 FANCD2, FANCD2OS
    nsv6549423inversion1nstd223human GRCh38 chr3: 10,089,203-10,089,667 , GRCh37.p13 chr3: 10,130,887-10,131,351 FANCD2OS, FANCD2
    nsv6546998inversion1nstd223human GRCh38 chr3: 10,102,144-10,102,763 , GRCh37.p13 chr3: 10,143,828-10,144,447 FANCD2, FANCD2OS
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