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 529

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6958261copy number variation1nstd229human GRCh38 chr15: 99,799,784-99,800,165 , GRCh37.p13 chr15: 100,339,989-100,340,370 DNM1P46
    nsv7146498copy number variation1nstd232human GRCh37.p13 chr15: 100,340,166-100,340,295 , GRCh38.p12 chr15: 99,799,961-99,800,090 DNM1P46
    nsv6498193copy number variation1nstd223human GRCh38 chr15: 99,803,601-99,804,200 , GRCh37.p13 chr15: 100,343,806-100,344,405 DNM1P46
    nsv6500617copy number variation1nstd223human GRCh38 chr15: 99,799,798-99,799,890 , GRCh37.p13 chr15: 100,340,003-100,340,095 DNM1P46
    nsv5529820copy number variation1nstd206human GRCh38 chr15: 99,799,759-99,800,208 , GRCh37.p13 chr15: 100,339,964-100,340,413 DNM1P46
    nsv6121161copy number variation1nstd186human GRCh37 chr15: 100,340,009-100,340,393 , GRCh38.p12 chr15: 99,799,804-99,800,188 DNM1P46
    nsv6203148copy number variation1nstd214human GRCh38 chr15: 99,799,846-99,800,001 , GRCh37.p13 chr15: 100,340,051-100,340,206 DNM1P46
    nsv6192737copy number variation1nstd214human GRCh38 chr15: 99,799,961-99,800,090 , GRCh37.p13 chr15: 100,340,166-100,340,295 DNM1P46
    nsv6273023copy number variation1nstd214human GRCh38 chr15: 99,798,430-99,798,531 , GRCh37.p13 chr15: 100,338,635-100,338,736 DNM1P46
    nsv6197876copy number variation1nstd214human GRCh38 chr15: 99,798,464-99,798,563 , GRCh37.p13 chr15: 100,338,669-100,338,768 DNM1P46
    nsv6205580copy number variation1nstd214human GRCh38 chr15: 99,800,073-99,800,169 , GRCh37.p13 chr15: 100,340,278-100,340,374 DNM1P46
    nsv6193960copy number variation1nstd214human GRCh38 chr15: 99,800,091-99,800,187 , GRCh37.p13 chr15: 100,340,296-100,340,392 DNM1P46
    nsv6189560copy number variation1nstd214human GRCh38 chr15: 99,800,103-99,800,199 , GRCh37.p13 chr15: 100,340,308-100,340,404 DNM1P46
    nsv6270489copy number variation1nstd214human GRCh38 chr15: 99,798,371-99,798,464 , GRCh37.p13 chr15: 100,338,576-100,338,669 DNM1P46
    nsv6205477copy number variation1nstd214human GRCh38 chr15: 99,799,825-99,799,915 , GRCh37.p13 chr15: 100,340,030-100,340,120 DNM1P46
    nsv6201517copy number variation1nstd214human GRCh38 chr15: 99,799,797-99,799,887 , GRCh37.p13 chr15: 100,340,002-100,340,092 DNM1P46
    nsv6196444copy number variation1nstd214human GRCh38 chr15: 99,799,807-99,799,895 , GRCh37.p13 chr15: 100,340,012-100,340,100 DNM1P46
    nsv6273661copy number variation1nstd214human GRCh38 chr15: 99,799,770-99,799,845 , GRCh37.p13 chr15: 100,339,975-100,340,050 DNM1P46
    nsv6274157copy number variation1nstd214human GRCh38 chr15: 99,799,937-99,800,001 , GRCh37.p13 chr15: 100,340,142-100,340,206 DNM1P46
    nsv6272428copy number variation1nstd214human GRCh38 chr15: 99,799,971-99,800,035 , GRCh37.p13 chr15: 100,340,176-100,340,240 DNM1P46
    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