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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112729copy number variation1nstd102humannot provided GRCh37 chr5: 116,419,511-120,022,321 , GRCh38.p12 chr5: 117,083,815-120,686,626 RN7SL174P, LINC02148, 35 more genes
    nsv5840722copy number variation1nstd209human GRCh38 chr5: 119,153,597-119,155,096 , GRCh37.p13 chr5: 118,489,292-118,490,791 DMXL1, MIR5706
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4872282inversion1nstd200human GRCh37 chr5: 98,106,197-132,803,784 , GRCh38.p12 chr5: 98,770,493-133,468,092 , LEAP2, 395 more genes
    nsv4676031copy number variation1nstd102humanUncertain significance GRCh37 chr5: 118,248,051-118,852,095 , GRCh38.p12 chr5: 118,912,356-119,516,400 LOC102723444, PTMAP2, 14 more genes
    nsv4675678copy number variation1nstd102humanUncertain significance GRCh37 chr5: 118,200,792-118,529,935 , GRCh38.p12 chr5: 118,865,097-119,194,240 DMXL1, PTMAP2, 9 more genes
    nsv4589930copy number variation1nstd183human GRCh37 chr5: 118,468,658-118,622,011 , GRCh38.p12 chr5: 119,132,963-119,286,316 DMXL1, TNFAIP8, 3 more genes
    nsv4456203copy number variation1nstd102humanUncertain significance GRCh37 chr5: 117,373,700-121,001,806 , GRCh38.p12 chr5: 118,038,005-121,666,111 RPL18P3, DMXL1-DT, 34 more genes
    nsv4456071copy number variation1nstd102humanPathogenic GRCh37 chr5: 108,304,806-121,335,239 , GRCh38.p12 chr5: 108,969,105-121,999,544 HMGN1P13, LOC101927023, 153 more genes
    nsv4455983copy number variation1nstd102humanPathogenic GRCh37 chr5: 89,949,118-129,317,455 , GRCh38.p12 chr5: 90,653,301-129,981,762 LOC345576, LOC107986436, 419 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4384659copy number variation1nstd173human GRCh37 chr5: 118,463,422-118,626,761 , GRCh38.p12 chr5: 119,127,727-119,291,066 DMXL1, TNFAIP8, 4 more genes
    nsv4382279copy number variation1nstd173human GRCh37 chr5: 118,462,868-118,626,761 , GRCh38.p12 chr5: 119,127,173-119,291,066 SEPTIN7P10, MIR5706, 4 more genes
    nsv4321173inversion1nstd166human GRCh37.p13 chr5: 86,365,040-130,339,409 , GRCh38.p12 chr5: 87,069,223-131,003,716 , APC, 481 more genes
    nsv4320566inversion1nstd166human GRCh37.p13 chr5: 114,283,102-148,759,757 , GRCh38.p12 chr5: 114,947,405-149,380,194 , ACTBP4, 606 more genes
    nsv4119754copy number variation1nstd166human GRCh37.p13 chr5: 118,257,722-118,490,053 , GRCh38.p12 chr5: 118,922,027-119,154,358 PTMAP2, SEPTIN7P10, 9 more genes
    nsv3956922copy number variation1nstd168human GRCh38 chr5: 118,941,934-119,223,391 , GRCh37.p13 chr5: 118,277,629-118,559,086 DMXL1, MIR1244-2, 9 more genes
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