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 313

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147076insertion1nstd232human GRCh37.p13 chr5: 137,767,257-137,767,257 , GRCh38.p12 chr5: 138,431,568-138,431,568 KDM3B
    nsv7143792insertion1nstd232human GRCh37.p13 chr5: 137,763,777-137,763,777 , GRCh38.p12 chr5: 138,428,088-138,428,088 KDM3B
    nsv7140097insertion1nstd232human GRCh37.p13 chr5: 137,761,271-137,761,271 , GRCh38.p12 chr5: 138,425,582-138,425,582 KDM3B
    nsv7097022copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,957,787-138,861,289 , GRCh38.p12 chr5: 137,622,098-139,481,704 CDC25C, SLC23A1, 55 more genes
    nsv7096751copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,957,787-140,078,137 , GRCh38.p12 chr5: 137,622,098-140,698,552 CDC25C, LOC100128966, 94 more genes
    nsv6796183copy number variation1nstd229human GRCh38 chr5: 138,357,650-138,360,883 , GRCh37.p13 chr5: 137,693,339-137,696,572 KDM3B
    nsv6793835copy number variation1nstd229human GRCh38 chr5: 138,039,501-138,538,500 , GRCh37.p13 chr5: 137,375,190-137,874,189 RNU6-460P, RNU6-1148P, 17 more genes
    nsv6787305copy number variation1nstd229human GRCh38 chr5: 138,378,786-138,378,814 , GRCh37.p13 chr5: 137,714,475-137,714,503 KDM3B
    nsv6785798copy number variation1nstd229human GRCh38 chr5: 138,357,850-138,358,339 , GRCh37.p13 chr5: 137,693,539-137,694,028 KDM3B
    nsv6782321copy number variation1nstd229human GRCh38 chr5: 138,400,530-138,402,267 , GRCh37.p13 chr5: 137,736,219-137,737,956 KDM3B
    nsv6780763copy number variation1nstd229human GRCh38 chr5: 138,368,314-138,368,348 , GRCh37.p13 chr5: 137,704,003-137,704,037 KDM3B
    nsv6574185inversion1nstd223human GRCh38 chr5: 138,370,823-138,371,277 , GRCh37.p13 chr5: 137,706,512-137,706,966 KDM3B
    nsv6567256inversion1nstd223human GRCh38 chr5: 138,406,105-138,407,221 , GRCh37.p13 chr5: 137,741,794-137,742,910 KDM3B
    nsv6565946inversion1nstd223human GRCh38 chr5: 138,422,411-138,422,967 , GRCh37.p13 chr5: 137,758,100-137,758,656 KDM3B
    nsv6565924inversion1nstd223human GRCh38 chr5: 138,384,385-138,385,319 , GRCh37.p13 chr5: 137,720,074-137,721,008 KDM3B
    nsv6563448inversion1nstd223human GRCh38 chr5: 138,367,888-138,368,461 , GRCh37.p13 chr5: 137,703,577-137,704,150 KDM3B
    nsv6563218inversion1nstd223human GRCh38 chr5: 138,413,322-138,413,802 , GRCh37.p13 chr5: 137,749,011-137,749,491 KDM3B
    nsv6563084inversion1nstd223human GRCh38 chr5: 138,395,922-138,397,339 , GRCh37.p13 chr5: 137,731,611-137,733,028 KDM3B
    nsv6561916inversion1nstd223human GRCh38 chr5: 138,383,159-138,383,698 , GRCh37.p13 chr5: 137,718,848-137,719,387 KDM3B
    nsv6559781inversion1nstd223human GRCh38 chr5: 138,404,349-138,404,794 , GRCh37.p13 chr5: 137,740,038-137,740,483 KDM3B
    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