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 949

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055263inversion1nstd229human GRCh38 chr5: 108,248,180-108,248,225 , GRCh37.p13 chr5: 107,583,881-107,583,926 FBXL17
    nsv7049880inversion1nstd229human GRCh38 chr5: 108,159,797-108,166,558 , GRCh37.p13 chr5: 107,495,498-107,502,259 FBXL17
    nsv7049376inversion1nstd229human GRCh38 chr5: 107,783,355-108,301,181 , GRCh37.p13 chr5: 107,119,056-107,636,882 RN7SKP122, FBXL17
    nsv7047442inversion1nstd229human GRCh38 chr5: 107,891,052-107,891,066 , GRCh37.p13 chr5: 107,226,753-107,226,767 FBXL17
    nsv7043464inversion1nstd229human GRCh38 chr5: 107,784,298-108,240,504 , GRCh37.p13 chr5: 107,119,999-107,576,205 FBXL17, RN7SKP122
    nsv7042567inversion1nstd229human GRCh38 chr5: 107,890,946-107,891,070 , GRCh37.p13 chr5: 107,226,647-107,226,771 FBXL17
    nsv7042543inversion1nstd229human GRCh38 chr5: 108,258,330-108,260,002 , GRCh37.p13 chr5: 107,594,031-107,595,703 FBXL17
    nsv6777869copy number variation1nstd229human GRCh38 chr5: 108,255,601-108,263,400 , GRCh37.p13 chr5: 107,591,302-107,599,101 FBXL17
    nsv6777717copy number variation1nstd229human GRCh38 chr5: 108,301,909-108,316,934 , GRCh37.p13 chr5: 107,637,610-107,652,635 FBXL17
    nsv6777376copy number variation1nstd229human GRCh38 chr5: 108,138,726-108,143,220 , GRCh37.p13 chr5: 107,474,427-107,478,921 FBXL17
    nsv6777297copy number variation1nstd229human GRCh38 chr5: 107,972,255-107,979,915 , GRCh37.p13 chr5: 107,307,956-107,315,616 FBXL17
    nsv6776847copy number variation1nstd229human GRCh38 chr5: 108,073,009-108,077,707 , GRCh37.p13 chr5: 107,408,710-107,413,408 FBXL17
    nsv6776549copy number variation1nstd229human GRCh38 chr5: 108,340,140-108,346,432 , GRCh37.p13 chr5: 107,675,841-107,682,133 FBXL17
    nsv6776513copy number variation1nstd229human GRCh38 chr5: 107,862,784-107,863,620 , GRCh37.p13 chr5: 107,198,485-107,199,321 FBXL17
    nsv6776217copy number variation1nstd229human GRCh38 chr5: 108,323,663-108,336,004 , GRCh37.p13 chr5: 107,659,364-107,671,705 FBXL17
    nsv6776147copy number variation1nstd229human GRCh38 chr5: 108,089,101-108,094,700 , GRCh37.p13 chr5: 107,424,802-107,430,401 FBXL17
    nsv6775852copy number variation1nstd229human GRCh38 chr5: 108,382,004-108,408,612 , GRCh37.p13 chr5: 107,717,705-107,744,313 FBXL17
    nsv6775574copy number variation1nstd229human GRCh38 chr5: 108,167,382-108,174,701 , GRCh37.p13 chr5: 107,503,083-107,510,402 FBXL17
    nsv6774872copy number variation1nstd229human GRCh38 chr5: 108,128,247-108,169,773 , GRCh37.p13 chr5: 107,463,948-107,505,474 FBXL17
    nsv6774254copy number variation1nstd229human GRCh38 chr5: 107,912,301-107,971,800 , GRCh37.p13 chr5: 107,248,002-107,307,501 FBXL17
    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