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 158

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048729inversion1nstd229human GRCh38 chr2: 10,950,861-12,841,358 , GRCh37.p13 chr2: 11,090,987-12,981,484 LOC101929752, LOC105373431, 34 more genes
    nsv7039094inversion1nstd229human GRCh38 chr2: 11,145,118-11,148,889 , GRCh37.p13 chr2: 11,285,244-11,289,015 C2orf50
    nsv6672827copy number variation1nstd229human GRCh38 chr2: 11,144,410-11,144,581 , GRCh37.p13 chr2: 11,284,536-11,284,707 C2orf50
    nsv6669169copy number variation1nstd229human GRCh38 chr2: 11,129,201-11,135,600 , GRCh37.p13 chr2: 11,269,327-11,275,726 FLJ33534, C2orf50
    nsv6668308copy number variation1nstd229human GRCh38 chr2: 11,128,114-11,136,457 , GRCh37.p13 chr2: 11,268,240-11,276,583 FLJ33534, C2orf50
    nsv6666576copy number variation1nstd229human GRCh38 chr2: 6,592,339-11,769,396 , GRCh37.p13 chr2: 6,732,471-11,909,522 RN7SKP112, LOC101929861, 103 more genes
    nsv6666172copy number variation1nstd229human GRCh38 chr2: 11,143,839-11,149,049 , GRCh37.p13 chr2: 11,283,965-11,289,175 C2orf50
    nsv6664647copy number variation1nstd229human GRCh38 chr2: 11,124,101-11,145,900 , GRCh37.p13 chr2: 11,264,227-11,286,026 FLJ33534, C2orf50
    nsv6664400copy number variation1nstd229human GRCh38 chr2: 11,145,601-11,149,400 , GRCh37.p13 chr2: 11,285,727-11,289,526 C2orf50
    nsv6662499copy number variation1nstd229human GRCh38 chr2: 10,913,620-11,157,722 , GRCh37.p13 chr2: 11,053,746-11,297,848 KCNF1, C2orf50, 3 more genes
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6306093insertion1nstd186human GRCh37 chr2: 11,285,244-11,285,244 , GRCh38.p12 chr2: 11,145,118-11,145,118 C2orf50
    nsv6290643copy number variation1nstd102humanUncertain significance GRCh37 chr2: 8,935,077-15,722,794 , GRCh38.p12 chr2: 8,794,947-15,582,670 PPIAP60, LOC105373431, 95 more genes
    nsv6290363copy number variation1nstd102humanUncertain significance GRCh37 chr2: 9,717,186-12,013,065 , GRCh38.p12 chr2: 9,577,057-11,872,939 RNU4-73P, CYS1, 56 more genes
    nsv5985557copy number variation1nstd212human GRCh38 chr2: 11,144,407-11,144,705 , GRCh37.p13 chr2: 11,284,533-11,284,831 C2orf50
    nsv5560849sequence alteration1nstd206human GRCh38 chr2: 11,145,117-11,148,889 , GRCh37.p13 chr2: 11,285,243-11,289,015 C2orf50
    nsv5535708insertion1nstd206human GRCh38 chr2: 11,145,118-11,145,118 , GRCh37.p13 chr2: 11,285,244-11,285,244 C2orf50
    nsv4763180insertion1nstd199human GRCh37 chr2: 11,290,815-11,290,815 , GRCh38.p12 chr2: 11,150,689-11,150,689 C2orf50
    nsv4728305copy number variation1nstd102humanUncertain significance GRCh37 chr2: 11,144,226-12,569,011 , GRCh38.p12 chr2: 11,004,100-12,428,885 RNA5SP85, TRG-CCC7-1, 30 more genes
    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