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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5869627copy number variation1nstd209human GRCh38 chr17: 75,844,028-75,845,096 , GRCh37.p13 chr17: 73,840,109-73,841,177 WBP2, UNC13D
    nsv5700257mobile element insertion1nstd211human GRCh38 chr17: 75,825,557-75,825,557 , GRCh37.p13 chr17: 73,821,638-73,821,638 UNC13D, UNK
    nsv5646828insertion1nstd207human GRCh38 chr17: 75,828,429-75,828,429 , GRCh37.p13 chr17: 73,824,510-73,824,510 UNC13D
    nsv5564314copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,824,026-73,826,583 , GRCh38.p12 chr17: 75,827,945-75,830,502 UNC13D
    nsv5526103copy number variation1nstd206human GRCh38 chr17: 75,825,964-75,826,058 , GRCh37.p13 chr17: 73,822,045-73,822,139 UNC13D, UNK
    nsv5432446mobile element insertion1nstd206human GRCh38 chr17: 75,825,557-75,825,608 , GRCh37.p13 chr17: 73,821,638-73,821,689 UNK, UNC13D
    nsv5293343copy number variation1nstd204human GRCh38.p13 chr17: 74,899,101-76,684,700 , GRCh37.p13 chr17: 72,895,199-74,680,782 , RNU6-24P, 92 more genes
    nsv5282319copy number variation1nstd204human GRCh38.p13 chr17: 75,609,901-75,917,300 , GRCh37.p13 chr17: 73,605,982-73,913,381 ITGB4, TRIM65, 15 more genes
    nsv5016711copy number variation1nstd200human GRCh38 chr17: 75,832,522-75,833,601 , GRCh37.p13 chr17: 73,828,603-73,829,682 UNC13D
    nsv4858994copy number variation1nstd200human GRCh37 chr17: 73,828,603-73,829,682 , GRCh38.p12 chr17: 75,832,522-75,833,601 UNC13D
    nsv4676104copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963 LLGL2, TSEN54, 165 more genes
    nsv4622832copy number variation1nstd183human GRCh37 chr17: 73,832,077-73,832,351 , GRCh38.p12 chr17: 75,835,996-75,836,270 UNC13D
    nsv4569850inversion1nstd166human GRCh37.p13 chr17: 73,573,022-73,825,589 , GRCh38.p12 chr17: 75,576,941-75,829,508 GALK1, H3-3B, 10 more genes
    nsv4515102mobile element insertion1nstd166human GRCh37.p13 chr17: 73,831,391-73,831,391 , GRCh38.p12 chr17: 75,835,310-75,835,310 UNC13D
    nsv4500590mobile element insertion1nstd166human GRCh37.p13 chr17: 73,821,624-73,821,624 , GRCh38.p12 chr17: 75,825,543-75,825,543 UNC13D, UNK
    nsv4457679copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,596,063-73,959,466 , GRCh38.p12 chr17: 75,599,982-75,963,385 MIR4738, RECQL5, 16 more genes
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4365771copy number variation1nstd173human GRCh37 chr17: 73,820,227-73,895,909 , GRCh38.p12 chr17: 75,824,146-75,899,828 WBP2, TRIM47, 4 more genes
    nsv3972399copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 64,159,738-74,891,024 , GRCh38.p12 chr17: 66,163,620-76,894,942 AANAT, ACOX1, 243 more genes
    nsv3919795copy number variation1nstd102humanPathogenic NCBI36 chr17: 71,144,026-71,478,420 , GRCh37 chr17: 73,632,431-73,966,825 , GRCh38 chr17: 75,636,351-75,970,744 ITGB4, TRIM65, 15 more genes
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