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 254

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098935copy number variation1nstd102humanUncertain significance GRCh38 chr17: 43,603,558-44,033,313 , GRCh37.p13 chr17: 41,680,926-42,110,681 LOC107985086, MPP2, 21 more genes
    nsv6990288copy number variation1nstd229human GRCh38 chr17: 44,058,680-44,062,668 , GRCh37.p13 chr17: 42,136,048-42,140,036 LSM12
    nsv6989325copy number variation1nstd229human GRCh38 chr17: 44,058,983-44,062,837 , GRCh37.p13 chr17: 42,136,351-42,140,205 LSM12
    nsv6985624copy number variation1nstd229human GRCh38 chr17: 44,058,469-44,062,663 , GRCh37.p13 chr17: 42,135,837-42,140,031 LSM12
    nsv6984480copy number variation1nstd229human GRCh38 chr17: 44,058,670-44,062,727 , GRCh37.p13 chr17: 42,136,038-42,140,095 LSM12
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6579455inversion1nstd223human GRCh38 chr17: 44,050,280-44,050,963 , GRCh37.p13 chr17: 42,127,648-42,128,331 LSM12
    nsv6511025copy number variation1nstd223human GRCh38 chr17: 44,058,706-44,062,779 , GRCh37.p13 chr17: 42,136,074-42,140,147 LSM12
    nsv6507595copy number variation1nstd223human GRCh38 chr17: 44,064,659-44,064,954 , GRCh37.p13 chr17: 42,142,027-42,142,322 LSM12
    nsv6506663copy number variation1nstd223human GRCh38 chr17: 44,058,131-44,060,017 , GRCh37.p13 chr17: 42,135,499-42,137,385 LSM12
    nsv6500992copy number variation1nstd223human GRCh38 chr17: 44,045,112-44,047,257 , GRCh37.p13 chr17: 42,122,480-42,124,625 LSM12
    nsv6500386copy number variation1nstd223human GRCh38 chr17: 44,056,736-44,057,500 , GRCh37.p13 chr17: 42,134,104-42,134,868 LSM12
    nsv6498056copy number variation1nstd223human GRCh38 chr17: 44,066,301-44,066,900 , GRCh37.p13 chr17: 42,143,669-42,144,268 LSM12
    nsv6291646copy number variation1nstd102humanUncertain significance GRCh37 chr17: 42,085,508-42,361,563 , GRCh38.p12 chr17: 44,008,140-44,284,195 LOC105371790, HDAC5, 16 more genes
    nsv6145451copy number variation1nstd206human GRCh38 chr17: 44,045,029-44,047,251 , GRCh37.p13 chr17: 42,122,397-42,124,619 LSM12
    nsv6133311copy number variation3nstd213human GRCh37 chr17: 41,970,000-42,760,001 , GRCh38.p12 chr17: 43,892,632-44,682,633 FZD2, GRN, 43 more genes
    nsv6029984copy number variation1nstd212human GRCh38 chr17: 44,045,304-44,047,013 , GRCh37.p13 chr17: 42,122,672-42,124,381 LSM12
    nsv6024705copy number variation1nstd212human GRCh38 chr17: 44,046,498-44,046,586 , GRCh37.p13 chr17: 42,123,866-42,123,954 LSM12
    nsv5933923copy number variation1nstd209human GRCh38 chr17: 44,036,338-44,036,930 , GRCh37.p13 chr17: 42,113,706-42,114,298 LSM12
    nsv5885735copy number variation1nstd209human GRCh38 chr17: 44,048,431-44,051,630 , GRCh37.p13 chr17: 42,125,799-42,128,998 LSM12
    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