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 182

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094367copy number variation1nstd102humanUncertain significance GRCh37 chr15: 34,567,526-34,635,274 , GRCh38.p12 chr15: 34,275,325-34,343,073 SLC12A6, NUTM1, 1 more genes
    nsv7094366copy number variation1nstd102humanPathogenic GRCh37 chr15: 34,526,072-35,087,019 , GRCh38.p12 chr15: 34,233,871-34,794,818 NUTM1, ACTC1, 16 more genes
    nsv7071130inversion1nstd229human GRCh38 chr15: 33,339,608-35,270,089 , GRCh37.p13 chr15: 33,631,809-35,562,290 LOC105370765, AQR, 38 more genes
    nsv7063469inversion1nstd229human GRCh38 chr15: 33,686,568-35,388,285 , GRCh37.p13 chr15: 33,978,769-35,680,486 NUTM1, AVEN, 41 more genes
    nsv6969948copy number variation1nstd229human GRCh38 chr15: 32,139,827-34,373,967 , GRCh37.p13 chr15: 32,432,028-34,666,168 AVEN, LPCAT4, 50 more genes
    nsv6634442copy number variation1nstd102humanPathogenic GRCh37 chr15: 32,915,722-34,671,601 , GRCh38.p12 chr15: 32,623,521-34,379,400 KATNBL1, ARHGAP11A, 27 more genes
    nsv6623245copy number variation1nstd224human GRCh37 chr15: 34,567,569-34,666,301 , GRCh38.p12 chr15: 34,275,368-34,374,100 LPCAT4, NOP10, 3 more genes
    nsv6502869copy number variation1nstd223human GRCh38 chr15: 33,970,001-34,711,900 , GRCh37.p13 chr15: 34,262,202-35,004,101 LINC02252, GOLGA8A, 20 more genes
    nsv6499953copy number variation1nstd223human GRCh38 chr15: 34,309,901-34,595,700 , GRCh37.p13 chr15: 34,602,102-34,887,901 LPCAT4, GOLGA8B, 12 more genes
    nsv6497589copy number variation1nstd223human GRCh38 chr15: 34,329,701-34,561,700 , GRCh37.p13 chr15: 34,621,902-34,853,901 SLC12A6, ACTG1P15, 12 more genes
    nsv6497505copy number variation1nstd223human GRCh38 chr15: 32,139,826-34,373,966 , GRCh37.p13 chr15: 32,432,027-34,666,167 TMCO5B, LPCAT4, 50 more genes
    nsv6315190copy number variation1nstd102humanPathogenic GRCh37 chr15: 33,809,650-40,027,263 , GRCh38.p12 chr15: 33,517,449-39,735,062 RYR3, RPL32P2, 84 more genes
    nsv6309784copy number variation1nstd102humanUncertain significance GRCh37 chr15: 34,526,082-35,087,009 , GRCh38.p12 chr15: 34,233,881-34,794,808 NUTM1, DNM1P5, 16 more genes
    nsv6309721copy number variation1nstd102humanUncertain significance GRCh37 chr15: 34,634,169-34,635,274 , GRCh38.p12 chr15: 34,341,968-34,343,073 NOP10, NUTM1
    nsv6132891copy number variation1nstd213human GRCh37 chr15: 34,380,000-34,660,001 , GRCh38.p12 chr15: 34,087,799-34,367,800 SLC12A6, EMC4, 6 more genes
    nsv5934855copy number variation1nstd209human GRCh38 chr15: 34,340,680-34,340,981 , GRCh37.p13 chr15: 34,632,881-34,633,182 NOP10
    nsv5856836copy number variation1nstd209human GRCh38 chr15: 34,338,609-34,342,230 , GRCh37.p13 chr15: 34,630,810-34,634,431 NOP10, NUTM1
    nsv5717515mobile element insertion1nstd211human GRCh38 chr15: 34,340,393-34,340,393 , GRCh37.p13 chr15: 34,632,594-34,632,594 NOP10
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5273531copy number variation1nstd204human GRCh38.p13 chr15: 33,908,501-34,437,400 , GRCh37.p13 chr15: 34,200,702-34,729,601 , GOLGA8A, 14 more genes
    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