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Items: 1 to 20 of 121

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148267copy number variation1nstd102humanPathogenic GRCh38 chr20: 87,153-23,635,465 , GRCh37.p13 chr20: 67,794-23,616,102 KRT18P3, RSPO4, 413 more genes
    nsv7096088copy number variation1nstd102humanUncertain significance GRCh37 chr20: 8,608,921-8,862,496 , GRCh38.p12 chr20: 8,628,274-8,881,849 LOC105372521, RNU105B, 1 more genes
    nsv7061818inversion1nstd229human GRCh38 chr20: 7,416,632-9,615,935 , GRCh37.p13 chr20: 7,397,279-9,596,582 RNU105B, RN7SL547P, 15 more genes
    nsv7035195copy number variation1nstd229human GRCh38 chr20: 8,740,721-8,922,615 , GRCh37.p13 chr20: 8,721,368-8,903,262 RNU105B, PLCB1
    nsv7032101copy number variation1nstd229human GRCh38 chr20: 8,742,916-9,418,528 , GRCh37.p13 chr20: 8,723,563-9,399,175 RNU105B, LOC105372522, 2 more genes
    nsv7032056copy number variation1nstd229human GRCh38 chr20: 8,791,423-8,864,459 , GRCh37.p13 chr20: 8,772,070-8,845,106 RNU105B, PLCB1
    nsv7028502copy number variation1nstd229human GRCh38 chr20: 7,054,114-8,875,895 , GRCh37.p13 chr20: 7,034,761-8,856,542 RNU105B, RN7SL547P, 13 more genes
    nsv7023763copy number variation1nstd229human GRCh38 chr20: 8,797,138-9,336,143 , GRCh37.p13 chr20: 8,777,785-9,316,790 PLCB1, PLCB4, 2 more genes
    nsv7022729copy number variation1nstd229human GRCh38 chr20: 7,235,562-10,519,088 , GRCh37.p13 chr20: 7,216,209-10,499,736 MKKS, PHKBP1, 30 more genes
    nsv7022067copy number variation1nstd229human GRCh38 chr20: 7,868,752-11,491,709 , GRCh37.p13 chr20: 7,849,399-11,472,357 LOC339593, LOC105372522, 36 more genes
    nsv7021544copy number variation1nstd229human GRCh38 chr20: 8,816,699-8,886,455 , GRCh37.p13 chr20: 8,797,346-8,867,102 RNU105B, PLCB1
    nsv6637576copy number variation1nstd102humanUncertain significance GRCh37 chr20: 8,725,348-9,399,410 , GRCh38.p12 chr20: 8,744,701-9,418,763 RNU105B, LOC105372522, 2 more genes
    nsv6626808copy number variation1nstd224human GRCh37 chr20: 8,783,279-9,308,828 , GRCh38.p12 chr20: 8,802,632-9,328,181 PLCB4, PLCB1, 2 more genes
    nsv6626733copy number variation1nstd224human GRCh37 chr20: 8,783,279-9,298,258 , GRCh38.p12 chr20: 8,802,632-9,317,611 PLCB4, PLCB1, 2 more genes
    nsv6534931copy number variation1nstd223human GRCh38 chr20: 8,742,916-9,418,531 , GRCh37.p13 chr20: 8,723,563-9,399,178 LOC105372522, RNU105B, 2 more genes
    nsv6315526copy number variation1nstd102humanPathogenic GRCh37 chr20: 3,178,539-11,848,383 , GRCh38.p12 chr20: 3,197,893-11,867,735 LRRN4, MCM8-AS1, 129 more genes
    nsv6314176copy number variation1nstd102humanUncertain significance GRCh37 chr20: 8,243,107-9,680,538 , GRCh38.p12 chr20: 8,262,460-9,699,890 LOC101929348, PLCB1, 8 more genes
    nsv6314008copy number variation1nstd102humanUncertain significance GRCh37 chr20: 8,720,511-9,398,938 , GRCh38.p12 chr20: 8,739,864-9,418,291 PLCB1, PLCB4, 2 more genes
    nsv6311245copy number variation1nstd102humanUncertain significance GRCh37 chr20: 7,812,350-10,654,278 , GRCh38.p12 chr20: 7,831,703-10,673,630 LOC100421490, RNU105B, 27 more genes
    nsv6311154copy number variation1nstd102humanUncertain significance GRCh37 chr20: 8,696,891-8,862,496 , GRCh38.p12 chr20: 8,716,244-8,881,849 RNU105B, PLCB1
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