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 83

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6408274copy number variation1nstd223human GRCh38 chr5: 180,927,801-181,343,300 , GRCh37.p13 chr5: 180,354,801-180,770,301 TRK-CTT2-2, ARPP19P1, 47 more genes
    nsv6400586copy number variation1nstd223human GRCh38 chr5: 181,356,401-181,357,300 , GRCh37.p13 chr5: 180,783,402-180,784,301 OR4F3
    nsv6141277copy number variation1nstd206human GRCh38 chr5: 181,353,324-181,364,000 , GRCh37.p13 chr5: 180,780,325-180,791,001 OR4F3
    nsv6140866copy number variation1nstd206human GRCh38 chr5: 181,353,000-181,368,000 , GRCh37.p13 chr5: 180,780,001-180,795,001 OR4F3
    nsv5666068inversion1nstd207human GRCh37.p13 chr5: 180,732,637-180,905,260 , GRCh38 chr5: 181,305,636-181,528,258 , OR4F3, 6 more genes
    nsv5633482insertion1nstd207human GRCh38 chr5: 181,343,337-181,343,337 , GRCh37.p13 chr5: 180,770,338-180,770,338 OR4F3
    nsv5624986insertion1nstd207human GRCh38 chr5: 181,341,819-181,341,819 , GRCh37.p13 chr5: 180,768,820-180,768,820 OR4F3
    nsv5584516copy number variation1nstd207human GRCh38 chr5: 181,341,801-181,341,858 , GRCh37.p13 chr5: 180,768,802-180,768,859 OR4F3
    nsv5235679copy number variation1nstd204human GRCh38.p13 chr5: 181,358,101-181,358,500 , GRCh37.p13 chr5: 180,785,102-180,785,501 OR4F3
    nsv5235587copy number variation1nstd204human GRCh38.p13 chr5: 181,348,501-181,367,900 , GRCh37.p13 chr5: 180,775,502-180,794,901 OR4F3
    nsv5232686copy number variation1nstd204human GRCh38.p13 chr5: 181,360,601-181,364,300 , GRCh37.p13 chr5: 180,787,602-180,791,301 OR4F3
    nsv5232013copy number variation1nstd204human GRCh38.p13 chr5: 181,359,001-181,359,700 , GRCh37.p13 chr5: 180,786,002-180,786,701 OR4F3
    nsv5229933copy number variation1nstd204human GRCh38.p13 chr5: 181,345,401-181,345,800 , GRCh37.p13 chr5: 180,772,402-180,772,801 OR4F3
    nsv5229857copy number variation1nstd204human GRCh38.p13 chr5: 181,356,201-181,356,700 , GRCh37.p13 chr5: 180,783,202-180,783,701 OR4F3
    nsv5227295copy number variation1nstd204human GRCh38.p13 chr5: 181,355,201-181,359,900 , GRCh37.p13 chr5: 180,782,202-180,786,901 OR4F3
    nsv5226735copy number variation1nstd204human GRCh38.p13 chr5: 181,356,201-181,365,800 , GRCh37.p13 chr5: 180,783,202-180,792,801 OR4F3
    nsv5226260copy number variation1nstd204human GRCh38.p13 chr5: 181,360,801-181,362,500 , GRCh37.p13 chr5: 180,787,802-180,789,501 OR4F3
    nsv5225959copy number variation1nstd204human GRCh38.p13 chr5: 181,366,201-181,366,900 , GRCh37.p13 chr5: 180,793,202-180,793,901 OR4F3
    nsv5225588copy number variation1nstd204human GRCh38.p13 chr5: 181,350,201-181,359,800 , GRCh37.p13 chr5: 180,777,202-180,786,801 OR4F3
    nsv5225271copy number variation1nstd204human GRCh38.p13 chr5: 181,354,201-181,355,000 , GRCh37.p13 chr5: 180,781,202-180,782,001 OR4F3
    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