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 110

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097206copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,109,903-53,164,416 , GRCh38.p12 chr3: 52,075,887-53,130,400 PHF7, SEMA3G, 47 more genes
    nsv7096959copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,485,283-52,485,425 , GRCh38.p12 chr3: 52,451,267-52,451,409 TNNC1
    nsv7096813copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,018,081-53,845,433 , GRCh38.p12 chr3: 51,984,065-53,811,406 DNAH1, BAP1, 62 more genes
    nsv7055197inversion1nstd229human GRCh38 chr3: 52,426,847-52,608,000 , GRCh37.p13 chr3: 52,460,863-52,642,016 STAB1, PBRM1, 7 more genes
    nsv6718083copy number variation1nstd229human GRCh38 chr3: 52,315,001-52,487,400 , GRCh37.p13 chr3: 52,349,017-52,521,416 BAP1, NISCH, 5 more genes
    nsv6711686copy number variation1nstd229human GRCh38 chr3: 51,850,901-52,533,900 , GRCh37.p13 chr3: 51,884,917-52,567,916 LOC105377088, GLYCTK-AS1, 37 more genes
    nsv6706848copy number variation1nstd229human GRCh38 chr3: 52,448,078-52,467,973 , GRCh37.p13 chr3: 52,482,094-52,501,989 NISCH, TNNC1
    nsv6701265copy number variation1nstd229human GRCh38 chr3: 52,454,200-52,454,314 , GRCh37.p13 chr3: 52,488,216-52,488,330 TNNC1, NISCH
    nsv6700890copy number variation1nstd229human GRCh38 chr3: 52,237,701-52,533,900 , GRCh37.p13 chr3: 52,271,717-52,567,916 STAB1, TWF2, 16 more genes
    nsv6369827copy number variation1nstd223human GRCh38 chr3: 52,164,358-54,467,618 , GRCh37.p13 chr3: 52,198,374-54,501,645 SEMA3G, STAB1, 61 more genes
    nsv6134815copy number variation1nstd213human GRCh37 chr3: 52,350,000-53,060,001 , GRCh38.p12 chr3: 52,315,984-53,025,985 ITIH1, ITIH3, 32 more genes
    nsv5891025copy number variation1nstd209human GRCh38 chr3: 49,693,626-52,462,904 , GRCh37.p13 chr3: 49,731,059-52,496,920 , SEMA3G, 106 more genes
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5449076copy number variation1nstd206human GRCh38 chr3: 52,454,193-52,454,319 , GRCh37.p13 chr3: 52,488,209-52,488,335 TNNC1, NISCH
    nsv5443022copy number variation1nstd206human GRCh38 chr3: 52,450,389-52,450,482 , GRCh37.p13 chr3: 52,484,405-52,484,498 TNNC1
    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
    nsv4911347copy number variation1nstd200human GRCh38 chr3: 51,769,352-52,724,007 , GRCh37.p13 chr3: 51,803,368-52,758,023 , ACY1, 55 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 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