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 591

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4684059copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 32,020,447-32,020,770 , GRCh38.p12 chr6: 32,052,670-32,052,993 TNXB
    nsv6137834copy number variation3nstd102humannot provided, Uncertain significance GRCh37 chr6: 32,064,182-32,064,367 , GRCh38 chr6: 32,096,405-32,096,590 TNXB
    nsv4578620copy number variation1nstd102humanUncertain significance GRCh37 chr6: 32,011,214-32,011,333 , GRCh38.p12 chr6: 32,043,437-32,043,556 TNXB
    nsv7093354copy number variation1nstd102humanUncertain significance GRCh37 chr6: 32,064,785-32,064,877 , GRCh38 chr6: 32,097,008-32,097,100 TNXB
    nsv6789478copy number variation1nstd229human GRCh38 chr6: 32,065,115-32,073,237 , GRCh37.p13 chr6: 32,032,892-32,041,014 TNXB
    nsv6788464copy number variation1nstd229human GRCh38 chr6: 32,060,854-32,066,818 , GRCh37.p13 chr6: 32,028,631-32,034,595 TNXB
    nsv6793008copy number variation1nstd229human GRCh38 chr6: 32,046,065-32,051,605 , GRCh37.p13 chr6: 32,013,842-32,019,382 TNXB
    nsv6795246copy number variation1nstd229human GRCh38 chr6: 32,081,338-32,086,729 , GRCh37.p13 chr6: 32,049,115-32,054,506 TNXB
    nsv6782544copy number variation1nstd229human GRCh38 chr6: 32,058,197-32,061,542 , GRCh37.p13 chr6: 32,025,974-32,029,319 TNXB
    nsv6399208copy number variation1nstd223human GRCh38 chr6: 32,061,876-32,068,107 , GRCh37.p13 chr6: 32,029,653-32,035,884 TNXB
    nsv6405009copy number variation1nstd223human GRCh38 chr6: 32,049,413-32,052,762 , GRCh37.p13 chr6: 32,017,190-32,020,539 TNXB
    nsv6411729copy number variation1nstd223human GRCh38 chr6: 32,058,201-32,060,500 , GRCh37.p13 chr6: 32,025,978-32,028,277 TNXB
    nsv5456987copy number variation1nstd206human GRCh38 chr6: 32,056,027-32,061,608 , GRCh37.p13 chr6: 32,023,804-32,029,385 TNXB
    nsv5472828copy number variation1nstd206human GRCh38 chr6: 32,053,585-32,056,783 , GRCh37.p13 chr6: 32,021,362-32,024,560 TNXB
    nsv5460556copy number variation1nstd206human GRCh38 chr6: 32,083,063-32,083,204 , GRCh37.p13 chr6: 32,050,840-32,050,981 TNXB
    nsv6305364copy number variation1nstd186human GRCh37 chr6: 32,023,804-32,029,385 , GRCh38.p12 chr6: 32,056,027-32,061,608 TNXB
    nsv5387082copy number variation1nstd186human GRCh37 chr6: 32,026,012-32,029,358 , GRCh38.p12 chr6: 32,058,235-32,061,581 TNXB
    nsv4663636copy number variation1nstd186human GRCh37 chr6: 32,025,932-32,029,271 , GRCh38.p12 chr6: 32,058,155-32,061,494 TNXB
    nsv5388756copy number variation1nstd186human GRCh37 chr6: 32,026,012-32,029,314 , GRCh38.p12 chr6: 32,058,235-32,061,537 TNXB
    nsv6009134copy number variation1nstd212human GRCh38 chr6: 32,056,162-32,058,071 , GRCh37.p13 chr6: 32,023,939-32,025,848 TNXB
    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