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 92934

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4668780copy number variation1nstd186human GRCh37 chr11: 54,694,268-55,038,507 , GRCh38.p12 chr11: 54,926,794-55,271,031 TRIM48
    nsv6296543copy number variation1nstd186human GRCh37 chr2: 15,164,814-15,488,597 , GRCh38.p12 chr2: 15,024,690-15,348,473 NBAS
    nsv6305340copy number variation1nstd186human GRCh37 chr9: 11,868,701-12,185,026 , GRCh38.p12 chr9: 11,868,701-12,185,026 LOC105375976
    nsv6305336copy number variation1nstd186human GRCh37 chr9: 11,910,508-12,175,174 , GRCh38.p12 chr9: 11,910,508-12,175,174 LOC105375976
    nsv6300550copy number variation1nstd186human GRCh37 chr4: 189,707,540-189,959,047 , GRCh38.p12 chr4: 188,786,386-189,037,893 LOC101930028
    nsv4658800copy number variation1nstd186human GRCh37 chr2: 205,898,770-206,130,221 , GRCh38.p12 chr2: 205,034,047-205,265,497 PARD3B
    nsv6303046copy number variation1nstd186human GRCh37 chr7: 125,839,025-126,063,945 , GRCh38.p12 chr7: 126,198,971-126,423,891 LOC105375488
    nsv4668748copy number variation1nstd186human GRCh37 chr9: 11,942,480-12,133,046 , GRCh38.p12 chr9: 11,942,480-12,133,046 LOC105375976
    nsv4658216copy number variation1nstd186human GRCh37 chr4: 168,808,583-168,992,985 , GRCh38.p12 chr4: 167,887,432-168,071,834 LOC105377523
    nsv4668472copy number variation1nstd186human GRCh37 chr8: 137,680,282-137,862,378 , GRCh38.p12 chr8: 136,668,039-136,850,135 LINC02055
    nsv4655448copy number variation2nstd186human GRCh37 chr8: 137,680,282-137,862,372 , GRCh38.p12 chr8: 136,668,039-136,850,129 LINC02055
    nsv4653621copy number variation1nstd186human GRCh37 chr8: 137,680,283-137,862,373 , GRCh38.p12 chr8: 136,668,040-136,850,130 LINC02055
    nsv4668626copy number variation1nstd186human GRCh37 chr8: 137,681,619-137,862,435 , GRCh38.p12 chr8: 136,669,376-136,850,192 LINC02055
    nsv4671269copy number variation1nstd186human GRCh37 chr8: 137,680,831-137,859,208 , GRCh38.p12 chr8: 136,668,588-136,846,965 LINC02055
    nsv6298292copy number variation1nstd186human GRCh37 chr5: 9,233,398-9,410,293 , GRCh38.p12 chr5: 9,233,286-9,410,181 SEMA5A
    nsv6297537copy number variation1nstd186human GRCh37 chr3: 7,868,660-8,033,865 , GRCh38.p12 chr3: 7,826,973-7,992,178 LOC101927394
    nsv4652865copy number variation1nstd186human GRCh37 chr6: 78,892,808-79,053,430 , GRCh38.p12 chr6: 78,183,091-78,343,713 LOC105377865
    nsv6297382copy number variation1nstd186human GRCh37 chr4: 98,575,081-98,730,571 , GRCh38.p12 chr4: 97,653,930-97,809,420 STPG2
    nsv6305666copy number variation1nstd186human GRCh37 chr8: 112,567,284-112,722,753 , GRCh38.p12 chr8: 111,555,055-111,710,524 H2AZP7
    nsv4644858copy number variation1nstd186human GRCh37 chr9: 132,654,988-132,798,900 , GRCh38.p12 chr9: 129,892,709-130,036,621 FNBP1
    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