U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 604

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5954388insertion1nstd209human GRCh38 chr4: 94,659,531-94,659,531 , GRCh37.p13 chr4: 95,580,682-95,580,682 PDLIM5
    nsv5947976insertion1nstd209human GRCh38 chr4: 94,492,115-94,492,115 , GRCh37.p13 chr4: 95,413,266-95,413,266 PDLIM5
    nsv5894896copy number variation1nstd209human GRCh38 chr4: 94,577,813-94,578,128 , GRCh37.p13 chr4: 95,498,964-95,499,279 PDLIM5
    nsv5731004mobile element insertion2nstd211human GRCh38 chr4: 94,622,284-94,622,284 , GRCh37.p13 chr4: 95,543,435-95,543,435 PDLIM5
    nsv5686365mobile element insertion2nstd211human GRCh38 chr4: 94,492,129-94,492,129 , GRCh37.p13 chr4: 95,413,280-95,413,280 PDLIM5
    nsv5681433mobile element insertion1nstd211human GRCh38 chr4: 94,527,890-94,527,890 , GRCh37.p13 chr4: 95,449,041-95,449,041 PDLIM5
    nsv5679446mobile element insertion1nstd211human GRCh38 chr4: 94,568,022-94,568,022 , GRCh37.p13 chr4: 95,489,173-95,489,173 PDLIM5
    nsv5678295mobile element insertion2nstd211human GRCh38 chr4: 94,454,226-94,454,226 , GRCh37.p13 chr4: 95,375,377-95,375,377 PDLIM5
    nsv5609274insertion1nstd207human GRCh38 chr4: 94,454,208-94,454,208 , GRCh37.p13 chr4: 95,375,359-95,375,359 PDLIM5
    nsv5608094insertion1nstd207human GRCh38 chr4: 94,473,144-94,473,144 , GRCh37.p13 chr4: 95,394,295-95,394,295 PDLIM5
    nsv5605215insertion1nstd207human GRCh38 chr4: 94,492,115-94,492,115 , GRCh37.p13 chr4: 95,413,266-95,413,266 PDLIM5
    nsv5571718copy number variation1nstd207human GRCh38 chr4: 94,577,813-94,578,128 , GRCh37.p13 chr4: 95,498,964-95,499,279 PDLIM5
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5559292mobile element insertion1nstd206human GRCh38 chr4: 94,622,284-94,622,335 , GRCh37.p13 chr4: 95,543,435-95,543,486 PDLIM5
    nsv5553422insertion1nstd206human GRCh38 chr4: 94,509,703-94,509,753 , GRCh37.p13 chr4: 95,430,854-95,430,904 PDLIM5
    nsv5552610insertion1nstd206human GRCh38 chr4: 94,492,129-94,492,180 , GRCh37.p13 chr4: 95,413,280-95,413,331 PDLIM5
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5465005copy number variation1nstd206human GRCh38 chr4: 94,577,823-94,578,129 , GRCh37.p13 chr4: 95,498,974-95,499,280 PDLIM5
    nsv5402557mobile element insertion1nstd206human GRCh38 chr4: 94,527,890-94,527,941 , GRCh37.p13 chr4: 95,449,041-95,449,092 PDLIM5
    nsv5401489mobile element insertion1nstd206human GRCh38 chr4: 94,568,022-94,568,073 , GRCh37.p13 chr4: 95,489,173-95,489,224 PDLIM5
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center