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 947

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138611copy number variation1nstd232human GRCh37.p13 chr5: 33,688,462-33,688,528 , GRCh38.p12 chr5: 33,688,357-33,688,423 ADAMTS12
    nsv7053355inversion1nstd229human GRCh38 chr5: 33,743,603-33,754,250 , GRCh37.p13 chr5: 33,743,708-33,754,355 ADAMTS12
    nsv7052596inversion1nstd229human GRCh38 chr5: 33,502,543-34,969,892 , GRCh37.p13 chr5: 33,502,648-34,969,997 TTC23L, DNAJC21, 22 more genes
    nsv7052166inversion1nstd229human GRCh38 chr5: 33,576,024-33,588,129 , GRCh37.p13 chr5: 33,576,129-33,588,234 ADAMTS12
    nsv7051931inversion1nstd229human GRCh38 chr5: 33,586,887-33,586,907 , GRCh37.p13 chr5: 33,586,992-33,587,012 ADAMTS12
    nsv7050117inversion1nstd229human GRCh38 chr5: 33,746,909-33,757,928 , GRCh37.p13 chr5: 33,747,014-33,758,033 ADAMTS12
    nsv7042714inversion1nstd229human GRCh38 chr5: 33,778,536-33,778,591 , GRCh37.p13 chr5: 33,778,641-33,778,696 ADAMTS12
    nsv7039407inversion1nstd229human GRCh38 chr5: 32,373,124-34,861,255 , GRCh37.p13 chr5: 32,373,230-34,861,360 TTC23L, LOC105374715, 31 more genes
    nsv6777073copy number variation1nstd229human GRCh38 chr5: 33,803,283-33,803,478 , GRCh37.p13 chr5: 33,803,388-33,803,583 ADAMTS12
    nsv6776805copy number variation1nstd229human GRCh38 chr5: 33,727,708-33,736,149 , GRCh37.p13 chr5: 33,727,813-33,736,254 ADAMTS12
    nsv6776698copy number variation1nstd229human GRCh38 chr5: 33,612,892-33,613,270 , GRCh37.p13 chr5: 33,612,997-33,613,375 ADAMTS12
    nsv6776322copy number variation1nstd229human GRCh38 chr5: 33,626,416-33,626,479 , GRCh37.p13 chr5: 33,626,521-33,626,584 ADAMTS12
    nsv6775816copy number variation1nstd229human GRCh38 chr5: 33,726,619-33,726,957 , GRCh37.p13 chr5: 33,726,724-33,727,062 ADAMTS12
    nsv6775554copy number variation1nstd229human GRCh38 chr5: 33,788,301-33,790,800 , GRCh37.p13 chr5: 33,788,406-33,790,905 ADAMTS12
    nsv6774673copy number variation1nstd229human GRCh38 chr5: 33,559,301-33,575,300 , GRCh37.p13 chr5: 33,559,406-33,575,405 ADAMTS12
    nsv6774158copy number variation1nstd229human GRCh38 chr5: 33,581,683-33,587,395 , GRCh37.p13 chr5: 33,581,788-33,587,500 ADAMTS12
    nsv6773810copy number variation1nstd229human GRCh38 chr5: 33,757,330-33,757,524 , GRCh37.p13 chr5: 33,757,435-33,757,629 ADAMTS12
    nsv6773620copy number variation1nstd229human GRCh38 chr5: 33,771,691-33,776,330 , GRCh37.p13 chr5: 33,771,796-33,776,435 ADAMTS12
    nsv6773343copy number variation1nstd229human GRCh38 chr5: 33,820,842-33,825,923 , GRCh37.p13 chr5: 33,820,947-33,826,028 ADAMTS12
    nsv6772338copy number variation1nstd229human GRCh38 chr5: 33,527,373-33,881,407 , GRCh37.p13 chr5: 33,527,478-33,881,512 ST3GAL5P1, ADAMTS12
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center