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 729

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137346insertion1nstd232human GRCh37.p13 chr5: 102,102,630-102,102,630 , GRCh38.p12 chr5: 102,766,926-102,766,926 PAM
    nsv7056938inversion1nstd229human GRCh38 chr5: 99,981,818-104,759,342 , GRCh37.p13 chr5: 99,317,522-104,095,043 PDZPH1P, ST8SIA4, 45 more genes
    nsv7052610inversion1nstd229human GRCh38 chr5: 101,750,339-102,838,301 , GRCh37.p13 chr5: 101,086,043-102,174,005 SLCO6A1, LINC00491, 8 more genes
    nsv7039797inversion1nstd229human GRCh38 chr5: 102,808,403-102,808,424 , GRCh37.p13 chr5: 102,144,107-102,144,128 PAM
    nsv7039153inversion1nstd229human GRCh38 chr5: 102,876,772-102,876,824 , GRCh37.p13 chr5: 102,212,476-102,212,528 PAM
    nsv6778053copy number variation1nstd229human GRCh38 chr5: 102,446,431-102,974,412 , GRCh37.p13 chr5: 101,782,135-102,310,116 LOC105379104, LINC00492, 3 more genes
    nsv6776541copy number variation1nstd229human GRCh38 chr5: 102,863,018-102,863,183 , GRCh37.p13 chr5: 102,198,722-102,198,887 PAM
    nsv6776057copy number variation1nstd229human GRCh38 chr5: 102,773,500-102,773,888 , GRCh37.p13 chr5: 102,109,204-102,109,592 PAM
    nsv6775555copy number variation1nstd229human GRCh38 chr5: 102,921,701-102,928,500 , GRCh37.p13 chr5: 102,257,405-102,264,204 PAM
    nsv6775136copy number variation1nstd229human GRCh38 chr5: 102,764,340-103,124,700 , GRCh37.p13 chr5: 102,100,044-102,420,837 LOC105379105, GIN1, 3 more genes
    nsv6774207copy number variation1nstd229human GRCh38 chr5: 102,945,165-102,946,402 , GRCh37.p13 chr5: 102,280,869-102,282,106 PAM
    nsv6773914copy number variation1nstd229human GRCh38 chr5: 102,882,574-102,889,863 , GRCh37.p13 chr5: 102,218,278-102,225,567 PAM
    nsv6773801copy number variation1nstd229human GRCh38 chr5: 103,017,434-103,028,180 , GRCh37.p13 chr5: 102,353,138-102,363,884 PAM
    nsv6773422copy number variation1nstd229human GRCh38 chr5: 102,829,930-102,842,960 , GRCh37.p13 chr5: 102,165,634-102,178,664 PAM
    nsv6773132copy number variation1nstd229human GRCh38 chr5: 102,974,401-103,046,600 , GRCh37.p13 chr5: 102,310,105-102,382,304 PAM, LOC105379105, 1 more genes
    nsv6772973copy number variation1nstd229human GRCh38 chr5: 102,853,871-102,853,927 , GRCh37.p13 chr5: 102,189,575-102,189,631 PAM
    nsv6772849copy number variation1nstd229human GRCh38 chr5: 102,938,599-102,943,713 , GRCh37.p13 chr5: 102,274,303-102,279,417 PAM
    nsv6772445copy number variation1nstd229human GRCh38 chr5: 102,979,461-102,985,048 , GRCh37.p13 chr5: 102,315,165-102,320,752 PAM
    nsv6772332copy number variation1nstd229human GRCh38 chr5: 102,827,669-102,827,903 , GRCh37.p13 chr5: 102,163,373-102,163,607 PAM
    nsv6771369copy number variation1nstd229human GRCh38 chr5: 102,988,235-102,988,392 , GRCh37.p13 chr5: 102,323,939-102,324,096 PAM
    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