U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Nucleotide

Items: 1 to 20 of 518

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146005copy number variation1nstd232human GRCh37.p13 chr5: 532,573-532,631 , GRCh38.p12 chr5: 532,458-532,516 , GRCh38.p12 chr5|NT_187550.1: 96,055-96,113 0
    nsv7143991copy number variation1nstd232human GRCh37.p13 chr5: 554,473-554,525 , GRCh38.p12 chr5: 554,358-554,410 , GRCh38.p12 chr5|NT_187550.1: 72,408-72,460 LOC105374606
    nsv7142576copy number variation1nstd232human GRCh37.p13 chr5: 505,722-505,840 , GRCh38.p12 chr5: 505,607-505,725 , GRCh38.p12 chr5|NT_187550.1: 122,846-122,964 SLC9A3
    nsv7139953insertion1nstd232human GRCh37.p13 chr5: 503,022-503,022 , GRCh38.p12 chr5: 502,907-502,907 , GRCh38.p12 chr5|NT_187550.1: 125,664-125,664 SLC9A3
    nsv7139499insertion1nstd232human GRCh37.p13 chr5: 543,352-543,352 , GRCh38.p12 chr5: 543,237-543,237 , GRCh38.p12 chr5|NT_187550.1: 85,334-85,334 0
    nsv6312202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 484,615-524,437 , GRCh38.p12 chr5|NT_187550.1: 104,249-126,136 , GRCh38.p12 chr5: 484,500-524,322 LOC107986395, SLC9A3
    nsv6299764copy number variation1nstd186human GRCh37 chr5: 517,576-517,745 , GRCh38.p12 chr5: 517,461-517,630 , GRCh38.p12 chr5|NT_187550.1: 110,941-111,110 SLC9A3
    nsv6299042copy number variation1nstd186human GRCh37 chr5: 555,253-556,637 , GRCh38.p12 chr5: 555,138-556,522 , GRCh38.p12 chr5|NT_187550.1: 70,375-71,759 LOC105374606
    nsv6297228copy number variation1nstd186human GRCh37 chr5: 610,949-611,102 , GRCh38.p12 chr5: 610,834-610,987 , GRCh38.p12 chr5|NT_187550.1: 15,910-16,063 CEP72, CEP72-DT, 1 more genes
    nsv6127906insertion1nstd186human GRCh37 chr5: 502,967-502,993 , GRCh38.p12 chr5: 502,852-502,878 , GRCh38.p12 chr5|NT_187550.1: 125,693-125,719 SLC9A3
    nsv5389166copy number variation1nstd186human GRCh37 chr5: 565,529-565,920 , GRCh38.p12 chr5: 565,414-565,805 , GRCh38.p12 chr5|NT_187550.1: 61,092-61,483 0
    nsv5389001copy number variation1nstd186human GRCh37 chr5: 557,671-558,130 , GRCh38.p12 chr5: 557,556-558,015 , GRCh38.p12 chr5|NT_187550.1: 68,882-69,341 LOC105374606
    nsv5388896copy number variation1nstd186human GRCh37 chr5: 536,927-537,243 , GRCh38.p12 chr5: 536,812-537,128 , GRCh38.p12 chr5|NT_187550.1: 91,443-91,759 MIR4456
    nsv5388375copy number variation1nstd186human GRCh37 chr5: 542,302-542,403 , GRCh38.p12 chr5: 542,187-542,288 , GRCh38.p12 chr5|NT_187550.1: 86,283-86,384 0
    nsv5387551copy number variation1nstd186human GRCh37 chr5: 557,745-557,988 , GRCh38.p12 chr5|NT_187550.1: 69,024-69,267 , GRCh38.p12 chr5: 557,630-557,873 LOC105374606
    nsv5387178copy number variation1nstd186human GRCh37 chr5: 557,575-557,889 , GRCh38.p12 chr5|NT_187550.1: 69,123-69,437 , GRCh38.p12 chr5: 557,460-557,774 LOC105374606
    nsv5386881copy number variation1nstd186human GRCh37 chr5: 557,535-558,163 , GRCh38.p12 chr5: 557,420-558,048 , GRCh38.p12 chr5|NT_187550.1: 68,849-69,477 LOC105374606
    nsv5385791copy number variation1nstd186human GRCh37 chr5: 565,543-565,840 , GRCh38.p12 chr5|NT_187550.1: 61,172-61,469 , GRCh38.p12 chr5: 565,428-565,725 0
    nsv4808438copy number variation1nstd200human GRCh37 chr5: 616,989-617,073 , GRCh38.p12 chr5|NT_187550.1: 9,939-10,023 , GRCh38.p12 chr5: 616,874-616,958 CEP72
    nsv4808437copy number variation1nstd200human GRCh37 chr5: 596,618-606,265 , GRCh38.p12 chr5: 596,503-606,150 , GRCh38.p12 chr5|NT_187550.1: 20,747-30,394 LOC105374608, CEP72-DT
    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