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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971027inversion1nstd209human GRCh38 chr5: 124,139,652-125,371,416 , GRCh37.p13 chr5: 123,475,345-124,707,109 ZNF608, RPL28P3, 11 more genes
    nsv5095594mobile element insertion1nstd203human GRCh38 chr5: 124,959,919-124,959,937 , GRCh37.p13 chr5: 124,295,612-124,295,630 LOC107986391
    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
    nsv4938347copy number variation1nstd200human GRCh38 chr5: 124,958,177-124,961,000 , GRCh37.p13 chr5: 124,293,870-124,296,693 LOC107986391
    nsv4938345copy number variation1nstd200human GRCh38 chr5: 124,937,624-124,952,363 , GRCh37.p13 chr5: 124,273,317-124,288,056 LOC107986391
    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
    nsv4803801copy number variation1nstd200human GRCh37 chr5: 124,295,228-124,295,864 , GRCh38.p12 chr5: 124,959,535-124,960,171 LOC107986391
    nsv4803800copy number variation1nstd200human GRCh37 chr5: 124,293,870-124,296,693 , GRCh38.p12 chr5: 124,958,177-124,961,000 LOC107986391
    nsv4803799copy number variation1nstd200human GRCh37 chr5: 124,273,317-124,288,056 , GRCh38.p12 chr5: 124,937,624-124,952,363 LOC107986391
    nsv4492192mobile element insertion1nstd166human GRCh37.p13 chr5: 124,299,375-124,299,375 , GRCh38.p12 chr5: 124,963,682-124,963,682 LOC107986391
    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
    nsv4345524sequence alteration1nstd166human GRCh37.p13 chr5: 120,941,265-127,230,417 , GRCh38.p12 chr5: 121,605,570-127,894,725 LOX, PPIC, 78 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
    nsv4123495copy number variation1nstd166human GRCh37.p13 chr5: 124,287,108-124,326,577 , GRCh38.p12 chr5: 124,951,415-124,990,884 LOC107986391, LOC105379158
    nsv3924205copy number variation1nstd102humanPathogenic GRCh37 chr5: 110,023,143-129,439,531 , GRCh38 chr5: 110,687,442-130,103,838 , NCBI36 chr5: 110,051,042-129,467,430 CSNK1G3, EPB41L4A-AS1, 231 more genes
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