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Items: 1 to 20 of 380

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146771copy number variation1nstd232human GRCh37.p13 chr12: 132,620,850-132,620,920 , GRCh38.p12 chr12: 132,136,305-132,136,375 DDX51
    nsv7137762copy number variation1nstd232human GRCh37.p13 chr12: 132,619,190-132,619,365 , GRCh38.p12 chr12: 132,134,645-132,134,820 DDX51
    nsv7093960copy number variation1nstd102humanUncertain significance GRCh37 chr12: 132,414,268-133,263,901 , GRCh38.p12 chr12: 131,929,723-132,687,315 LOC107987169, NOC4L, 20 more genes
    nsv7074381inversion1nstd229human GRCh38 chr12: 132,139,541-132,164,040 , GRCh37.p13 chr12: 132,624,086-132,648,585 DDX51, NOC4L
    nsv7074199inversion1nstd229human GRCh38 chr12: 123,186,434-132,825,682 , GRCh37.p13 chr12: 123,670,981-133,402,268 PIWIL1, FZD10-AS1, 187 more genes
    nsv7073598inversion1nstd229human GRCh38 chr12: 131,876,394-132,174,026 , GRCh37.p13 chr12: 132,360,939-132,658,571 NOC4L, DDX51, 7 more genes
    nsv7073229inversion1nstd229human GRCh38 chr12: 132,098,464-132,282,395 , GRCh37.p13 chr12: 132,583,009-132,706,992 DDX51, LINC02361, 6 more genes
    nsv7072321inversion1nstd229human GRCh38 chr12: 131,976,015-132,309,484 , GRCh37.p13 chr12: 132,460,560-132,706,992 LOC105370091, NOC4L, 8 more genes
    nsv7071385inversion1nstd229human GRCh38 chr12: 131,514,757-132,281,110 , GRCh37.p13 chr12: 131,999,302-132,706,992 LINC02361, EP400, 24 more genes
    nsv7069228inversion1nstd229human GRCh38 chr12: 131,736,676-132,414,978 , GRCh37.p13 chr12: 132,221,221-132,991,564 LOC107987169, NOC4L, 17 more genes
    nsv7067298inversion1nstd229human GRCh38 chr12: 132,079,777-132,851,356 , GRCh37.p13 chr12: 132,564,322-133,427,942 LRCOL1, PGAM5, 26 more genes
    nsv6932192copy number variation1nstd229human GRCh38 chr12: 132,038,649-132,478,593 , GRCh37.p13 chr12: 132,523,194-133,055,179 EP400P1, LOC112268102, 11 more genes
    nsv6930874copy number variation1nstd229human GRCh38 chr12: 132,002,630-132,150,775 , GRCh37.p13 chr12: 132,487,175-132,635,320 EP400P1, EP400, 4 more genes
    nsv6930484copy number variation1nstd229human GRCh38 chr12: 132,062,312-132,288,002 , GRCh37.p13 chr12: 132,546,857-132,706,992 GALNT9, DDX51, 7 more genes
    nsv6930377copy number variation1nstd229human GRCh38 chr12: 132,140,033-132,420,483 , GRCh37.p13 chr12|NW_003315937.1: 1-165,247 , GRCh37.p13 chr12: 132,624,578-132,997,069 GALNT9-AS1, GALNT9, 5 more genes
    nsv6924095copy number variation1nstd229human GRCh38 chr12: 131,969,836-132,136,681 , GRCh37.p13 chr12: 132,454,381-132,621,226 EP400P1, EP400, 3 more genes
    nsv6920981copy number variation1nstd229human GRCh38 chr12: 132,073,459-132,447,802 , GRCh37.p13 chr12: 132,558,004-133,024,388 GALNT9-AS1, DDX51, 10 more genes
    nsv6918342copy number variation1nstd229human GRCh38 chr12: 132,140,346-132,146,519 , GRCh37.p13 chr12: 132,624,891-132,631,064 DDX51, NOC4L
    nsv6492719copy number variation1nstd223human GRCh38 chr12: 131,582,101-132,134,800 , GRCh37.p13 chr12: 132,066,646-132,619,345 EP400, LOC100996701, 18 more genes
    nsv6490508copy number variation1nstd223human GRCh38 chr12: 132,121,050-132,183,296 , GRCh37.p13 chr12: 132,605,595-132,667,841 EP400P1, LOC107987169, 2 more genes
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