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 147

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5904127copy number variation1nstd209human GRCh38 chr3: 9,996,659-11,875,087 , GRCh37.p13 chr3: 10,038,343-11,916,561 , EMC3, 35 more genes
    nsv5901270copy number variation1nstd209human GRCh38 chr3: 10,048,544-11,870,471 , GRCh37.p13 chr3: 10,090,228-11,911,945 , SLC6A11, 29 more genes
    nsv5891525copy number variation1nstd209human GRCh38 chr3: 9,996,478-11,874,953 , GRCh37.p13 chr3: 10,038,162-11,916,427 , TATDN2, 35 more genes
    nsv5673471copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 10,091,048-10,140,634 , GRCh38.p12 chr3: 10,049,364-10,098,950 FANCD2, FANCD2OS, 1 more genes
    nsv5381364copy number variation1nstd102humanUncertain significance GRCh37 chr3: 9,976,103-10,191,669 , GRCh38.p12 chr3: 9,934,419-10,149,985 CYCSP10, MARK2P2, 13 more genes
    nsv5311699copy number variation1nstd204human GRCh38.p13 chr3: 9,776,127-10,149,069 , GRCh37.p13 chr3: 9,817,811-10,190,753 EMC3, CYCSP11, 25 more genes
    nsv5205129copy number variation1nstd204human GRCh38.p13 chr3: 9,776,301-10,148,700 , GRCh37.p13 chr3: 9,817,985-10,190,384 JAGN1, TTLL3, 25 more genes
    nsv5203086copy number variation1nstd204human GRCh38.p13 chr3: 10,048,238-10,091,912 , GRCh37.p13 chr3: 10,089,922-10,133,596 FANCD2OS, FANCD2, 1 more genes
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4743065copy number variation1nstd199human GRCh37 chr3: 10,036,258-11,911,948 , GRCh38.p12 chr3: 9,994,574-11,870,474 , ATP2B2-IT2, 36 more genes
    nsv4738819copy number variation1nstd199human GRCh37 chr3: 10,090,229-11,911,947 , GRCh38.p12 chr3: 10,048,545-11,870,473 , LINC00852, 29 more genes
    nsv4684163copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,091,190-10,101,977 , GRCh38.p12 chr3: 10,049,506-10,060,293 FANCD2, CYCSP11
    nsv4681192copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr3: 10,094,061-10,191,719 , GRCh38.p12 chr3: 10,052,377-10,150,035 FANCD2OS, CYCSP11, 3 more genes
    nsv4674715copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-10,287,825 , GRCh38.p12 chr3: 20,213-10,246,141 LOC105376944, LMCD1, 122 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4468477mobile element insertion1nstd166human GRCh37.p13 chr3: 10,100,225-10,100,225 , GRCh38.p12 chr3: 10,058,541-10,058,541 CYCSP11, FANCD2
    nsv4450930copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr3: 10,094,061-10,191,659 , GRCh38 chr3: 10,052,377-10,149,975 FANCD2, VHL, 3 more genes
    nsv4435930copy number variation1nstd102humanUncertain significance GRCh37 chr3: 9,453,917-12,015,126 , GRCh38.p12 chr3: 9,412,233-11,973,652 VGLL4, JAGN1, 63 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