U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 14135

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3221307copy number variation3nstd152human GRCh38 chr11: 55,086,811-55,286,227 , GRCh37.p13 chr11: 54,854,287-55,053,703 TRIM48
    nsv3196425copy number variation3nstd152human GRCh38 chrX: 99,625,549-99,779,146 , GRCh37.p13 chrX: 98,880,547-99,034,144 XRCC6P5
    nsv3208327copy number variation6nstd152human GRCh38 chr2: 97,429,764-97,582,282 , GRCh37.p13 chr2: 98,095,344-98,198,745 ANKRD36B
    nsv3221600copy number variation9nstd152human GRCh38 chr11: 70,934,772-71,067,280 , GRCh37.p13 chr11|NW_004070871.1: 478,985-561,493 SHANK2
    nsv3190753copy number variation8nstd152human GRCh38 chr4: 21,075,739-21,206,721 , GRCh37.p13 chr4: 21,077,362-21,208,344 KCNIP4
    nsv3217926copy number variation2nstd152human GRCh38 chr9: 65,899,143-66,021,230 , GRCh37.p13 chr9: 42,879,721-43,001,808 AQP7P3
    nsv3221159copy number variation9nstd152human GRCh38 chr15: 68,046,399-68,164,345 , GRCh37.p13 chr15: 68,338,737-68,456,683 PIAS1
    nsv3204913copy number variation1nstd152human GRCh38 chr2: 56,557,577-56,666,665 , GRCh37.p13 chr2: 56,784,712-56,893,800 LOC101927213
    nsv3204488copy number variation2nstd152human GRCh38 chr1: 169,183,581-169,288,506 , GRCh37.p13 chr1: 169,152,819-169,257,744 NME7
    nsv3195540copy number variation1nstd152human GRCh38 chr5: 19,808,779-19,913,598 , GRCh37.p13 chr5: 19,808,888-19,913,707 CDH18
    nsv3196009copy number variation1nstd152human GRCh38 chr2: 156,622,607-156,726,566 , GRCh37.p13 chr2: 157,479,119-157,583,078 LINC01958
    nsv3193372copy number variation2nstd152human GRCh38 chr1: 95,980,568-96,083,906 , GRCh37.p13 chr1: 96,446,124-96,549,462 LINC02790
    nsv3220078copy number variation2nstd152human GRCh38 chr8: 137,637,342-137,733,308 , GRCh37.p13 chr8: 138,649,585-138,745,551 LOC100129367
    nsv3218194copy number variation9nstd152human GRCh38 chr7: 96,824,384-96,919,001 , GRCh37.p13 chr7: 96,453,696-96,548,313 MARK2P10
    nsv3197073copy number variation3nstd152human GRCh38 chr2: 97,182,957-97,275,452 , GRCh37.p13 chr2: 97,848,694-97,941,189 ANKRD36
    nsv3219580copy number variation1nstd152human GRCh38 chr11: 24,058,494-24,150,190 , GRCh37.p13 chr11: 24,080,040-24,171,736 LOC107984378
    nsv3190804copy number variation3nstd152human GRCh38 chr4: 52,260,331-52,351,868 , GRCh37.p13 chr4: 53,126,497-53,218,034 LOC107986279
    nsv3218776copy number variation1nstd152human GRCh38 chr15: 68,074,007-68,164,345 , GRCh37.p13 chr15: 68,366,345-68,456,683 PIAS1
    nsv3190695copy number variation9nstd152human GRCh38 chr4: 180,895,149-180,984,192 , GRCh37.p13 chr4: 181,816,302-181,905,345 LOC105377568
    nsv3195581copy number variation9nstd152human GRCh38 chr6: 133,015,998-133,104,809 , GRCh37.p13 chr6: 133,337,137-133,425,948 LINC00326
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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