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 1236

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056427inversion1nstd229human GRCh38 chr2: 170,422,793-170,422,847 , GRCh37.p13 chr2: 171,279,303-171,279,357 MYO3B
    nsv7050593inversion1nstd229human GRCh38 chr2: 170,413,882-170,415,659 , GRCh37.p13 chr2: 171,270,392-171,272,169 MYO3B
    nsv7049857inversion1nstd229human GRCh38 chr2: 170,566,115-170,682,505 , GRCh37.p13 chr2: 171,422,625-171,539,015 HMGB1P4, MYO3B, 1 more genes
    nsv7049540inversion1nstd229human GRCh38 chr2: 170,441,257-170,456,003 , GRCh37.p13 chr2: 171,297,767-171,312,513 MYO3B
    nsv7049091inversion1nstd229human GRCh38 chr2: 170,509,158-170,521,572 , GRCh37.p13 chr2: 171,365,668-171,378,082 MYO3B
    nsv7047618inversion1nstd229human GRCh38 chr2: 170,182,859-170,189,974 , GRCh37.p13 chr2: 171,039,369-171,046,484 MYO3B
    nsv7047133inversion1nstd229human GRCh38 chr2: 170,627,743-170,630,869 , GRCh37.p13 chr2: 171,484,253-171,487,379 LOC100130256, MYO3B
    nsv7043764inversion1nstd229human GRCh38 chr2: 169,756,513-170,924,608 , GRCh37.p13 chr2: 170,613,023-171,781,118 LINC01124, METTL5, 17 more genes
    nsv7041078inversion1nstd229human GRCh38 chr2: 170,573,089-170,573,103 , GRCh37.p13 chr2: 171,429,599-171,429,613 MYO3B
    nsv7039743inversion1nstd229human GRCh38 chr2: 170,630,871-170,641,163 , GRCh37.p13 chr2: 171,487,381-171,497,673 MYO3B, LOC100130256
    nsv6697888copy number variation1nstd229human GRCh38 chr2: 170,429,158-170,439,645 , GRCh37.p13 chr2: 171,285,668-171,296,155 MYO3B
    nsv6697695copy number variation1nstd229human GRCh38 chr2: 170,223,345-170,223,701 , GRCh37.p13 chr2: 171,079,855-171,080,211 MYO3B
    nsv6697518copy number variation1nstd229human GRCh38 chr2: 170,390,755-170,395,233 , GRCh37.p13 chr2: 171,247,265-171,251,743 MYO3B
    nsv6697372copy number variation1nstd229human GRCh38 chr2: 169,988,465-170,447,481 , GRCh37.p13 chr2: 170,844,975-171,303,991 NSA2P5, UBR3, 3 more genes
    nsv6696862copy number variation1nstd229human GRCh38 chr2: 170,515,922-170,519,240 , GRCh37.p13 chr2: 171,372,432-171,375,750 MYO3B
    nsv6696713copy number variation1nstd229human GRCh38 chr2: 170,279,101-170,283,100 , GRCh37.p13 chr2: 171,135,611-171,139,610 MYO3B
    nsv6696286copy number variation1nstd229human GRCh38 chr2: 170,333,869-170,339,173 , GRCh37.p13 chr2: 171,190,379-171,195,683 MYO3B, MYO3B-AS1
    nsv6695727copy number variation1nstd229human GRCh38 chr2: 170,425,642-170,428,776 , GRCh37.p13 chr2: 171,282,152-171,285,286 MYO3B
    nsv6694813copy number variation1nstd229human GRCh38 chr2: 170,555,701-170,557,700 , GRCh37.p13 chr2: 171,412,211-171,414,210 MYO3B
    nsv6694304copy number variation1nstd229human GRCh38 chr2: 170,327,453-170,327,497 , GRCh37.p13 chr2: 171,183,963-171,184,007 MYO3B
    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