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 1062

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974516inversion1nstd209human GRCh38 chr6: 38,423,787-38,431,607 , GRCh37.p13 chr6: 38,391,563-38,399,383 BTBD9
    nsv5969731inversion1nstd209human GRCh38 chr6: 38,436,726-38,442,134 , GRCh37.p13 chr6: 38,404,502-38,409,910 BTBD9
    nsv5965951insertion1nstd209human GRCh38 chr6: 38,607,628-38,607,628 , GRCh37.p13 chr6: 38,575,404-38,575,404 BTBD9
    nsv5958530insertion1nstd209human GRCh38 chr6: 38,627,932-38,627,932 , GRCh37.p13 chr6: 38,595,708-38,595,708 BTBD9
    nsv5950156insertion1nstd209human GRCh38 chr6: 38,527,801-38,527,801 , GRCh37.p13 chr6: 38,495,577-38,495,577 BTBD9
    nsv5949703insertion1nstd209human GRCh38 chr6: 38,205,891-38,205,891 , GRCh37.p13 chr6: 38,173,667-38,173,667 BTBD9
    nsv5906183copy number variation1nstd209human GRCh38 chr6: 38,303,277-38,304,713 , GRCh37.p13 chr6: 38,271,053-38,272,489 BTBD9
    nsv5905415copy number variation1nstd209human GRCh38 chr6: 38,261,213-38,261,442 , GRCh37.p13 chr6: 38,228,989-38,229,218 BTBD9
    nsv5902759copy number variation1nstd209human GRCh38 chr6: 38,497,987-38,498,094 , GRCh37.p13 chr6: 38,465,763-38,465,870 BTBD9
    nsv5899437copy number variation1nstd209human GRCh38 chr6: 38,216,957-38,219,869 , GRCh37.p13 chr6: 38,184,733-38,187,645 BTBD9
    nsv5895605copy number variation1nstd209human GRCh38 chr6: 38,530,502-38,530,638 , GRCh37.p13 chr6: 38,498,278-38,498,414 BTBD9
    nsv5893713copy number variation1nstd209human GRCh38 chr6: 38,243,025-38,243,093 , GRCh37.p13 chr6: 38,210,801-38,210,869 BTBD9, LOC105375045
    nsv5889397copy number variation1nstd209human GRCh38 chr6: 38,312,051-38,314,386 , GRCh37.p13 chr6: 38,279,827-38,282,162 BTBD9
    nsv5889300copy number variation1nstd209human GRCh38 chr6: 38,312,297-38,312,561 , GRCh37.p13 chr6: 38,280,073-38,280,337 BTBD9
    nsv5888483copy number variation1nstd209human GRCh38 chr6: 38,402,249-38,402,451 , GRCh37.p13 chr6: 38,370,025-38,370,227 BTBD9
    nsv5845595copy number variation1nstd209human GRCh38 chr6: 38,303,255-38,304,747 , GRCh37.p13 chr6: 38,271,031-38,272,523 BTBD9
    nsv5845594copy number variation1nstd209human GRCh38 chr6: 38,217,723-38,220,122 , GRCh37.p13 chr6: 38,185,499-38,187,898 BTBD9
    nsv5844953copy number variation1nstd209human GRCh38 chr6: 38,423,744-38,436,731 , GRCh37.p13 chr6: 38,391,520-38,404,507 BTBD9
    nsv5844952copy number variation1nstd209human GRCh38 chr6: 38,219,373-38,223,886 , GRCh37.p13 chr6: 38,187,149-38,191,662 BTBD9
    nsv5844890copy number variation1nstd209human GRCh38 chr6: 38,311,982-38,314,414 , GRCh37.p13 chr6: 38,279,758-38,282,190 BTBD9
    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