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 1028

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147195copy number variation1nstd232human GRCh37.p13 chr17: 31,087,422-31,087,498 , GRCh38.p12 chr17: 32,760,404-32,760,480 MYO1D
    nsv7140519copy number variation1nstd232human GRCh37.p13 chr17: 30,904,218-30,904,277 , GRCh38.p12 chr17: 32,577,200-32,577,259 MYO1D
    nsv7140493insertion1nstd232human GRCh37.p13 chr17: 31,065,406-31,065,406 , GRCh38.p12 chr17: 32,738,388-32,738,388 MYO1D
    nsv7137216copy number variation1nstd102humanPathogenic GRCh37 chr17: 30,572,862-35,843,988 , GRCh38.p12 chr17: 32,245,843-36,446,544 PSMD11, C17orf50, 117 more genes
    nsv7072535inversion1nstd229human GRCh38 chr17: 32,763,548-32,763,643 , GRCh37.p13 chr17: 31,090,566-31,090,661 MYO1D
    nsv7071694inversion1nstd229human GRCh38 chr17: 32,646,676-32,650,393 , GRCh37.p13 chr17: 30,973,694-30,977,411 MYO1D
    nsv7061757inversion1nstd229human GRCh38 chr17: 32,751,004-32,751,053 , GRCh37.p13 chr17: 31,078,022-31,078,071 MYO1D
    nsv7061227inversion1nstd229human GRCh38 chr17: 32,866,159-32,869,461 , GRCh37.p13 chr17: 31,193,177-31,196,479 MYO1D
    nsv7058412inversion1nstd229human GRCh38 chr17: 30,021,943-32,643,975 , GRCh37.p13 chr17: 28,348,961-30,970,993 RNU6-990P, LOC105371730, 81 more genes
    nsv6997863copy number variation1nstd229human GRCh38 chr17: 32,620,621-32,625,918 , GRCh37.p13 chr17: 30,947,639-30,952,936 MYO1D
    nsv6997655copy number variation1nstd229human GRCh38 chr17: 32,552,797-32,712,542 , GRCh37.p13 chr17: 30,879,815-31,039,560 MYO1D
    nsv6996590copy number variation1nstd229human GRCh38 chr17: 32,660,748-32,661,717 , GRCh37.p13 chr17: 30,987,766-30,988,735 MYO1D
    nsv6996512copy number variation1nstd229human GRCh38 chr17: 32,671,301-32,731,900 , GRCh37.p13 chr17: 30,998,319-31,058,918 MYO1D
    nsv6996356copy number variation1nstd229human GRCh38 chr17: 32,582,691-32,586,317 , GRCh37.p13 chr17: 30,909,709-30,913,335 MYO1D
    nsv6996106copy number variation1nstd229human GRCh38 chr17: 32,577,201-32,577,260 , GRCh37.p13 chr17: 30,904,219-30,904,278 MYO1D
    nsv6995992copy number variation1nstd229human GRCh38 chr17: 32,830,677-32,830,753 , GRCh37.p13 chr17: 31,157,695-31,157,771 MYO1D
    nsv6995368copy number variation1nstd229human GRCh38 chr17: 32,550,978-32,551,071 , GRCh37.p13 chr17: 30,877,996-30,878,089 MYO1D
    nsv6994302copy number variation1nstd229human GRCh38 chr17: 32,839,578-32,854,335 , GRCh37.p13 chr17: 31,166,596-31,181,353 MYO1D
    nsv6993218copy number variation1nstd229human GRCh38 chr17: 32,603,848-32,606,777 , GRCh37.p13 chr17: 30,930,866-30,933,795 MYO1D
    nsv6993067copy number variation1nstd229human GRCh38 chr17: 32,868,418-32,868,508 , GRCh37.p13 chr17: 31,195,436-31,195,526 MYO1D
    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