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 159

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906893copy number variation1nstd209human GRCh38 chr5: 33,948,938-33,949,038 , GRCh37.p13 chr5: 33,949,043-33,949,143 SLC45A2
    nsv5905047copy number variation1nstd209human GRCh38 chr5: 33,967,721-33,968,268 , GRCh37.p13 chr5: 33,967,826-33,968,373 SLC45A2
    nsv5901227copy number variation1nstd209human GRCh38 chr5: 33,984,986-33,985,073 , GRCh37.p13 chr5: 33,985,091-33,985,178 AMACR, SLC45A2, 1 more genes
    nsv5716520mobile element insertion1nstd211human GRCh38 chr5: 33,952,514-33,952,514 , GRCh37.p13 chr5: 33,952,619-33,952,619 SLC45A2
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5468339copy number variation1nstd206human GRCh38 chr5: 33,967,721-33,968,272 , GRCh37.p13 chr5: 33,967,826-33,968,377 SLC45A2
    nsv5381781copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,081,195-45,294,031 , GRCh38.p12 chr5: 29,081,088-45,293,929 ST3GAL5P1, LOC105374711, 213 more genes
    nsv5368131translocation1nstd200human GRCh38 chr5: 33,968,272-33,968,272 , GRCh38 chr5: 33,967,721-33,967,721 , GRCh37.p13 chr5: 33,968,377-33,968,377 , GRCh37.p13 chr5: 33,967,826-33,967,826 SLC45A2
    nsv5338988translocation1nstd200human GRCh37 chr5: 33,967,826-33,967,826 , GRCh37 chr5: 33,968,377-33,968,377 , GRCh38.p12 chr5: 33,968,272-33,968,272 , GRCh38.p12 chr5: 33,967,721-33,967,721 SLC45A2
    nsv5335310translocation1nstd200human GRCh37 chr5: 33,949,046-33,949,046 , GRCh37 chr5: 33,949,144-33,949,144 , GRCh38.p12 chr5: 33,949,039-33,949,039 , GRCh38.p12 chr5|NT_187551.1: 150,263-150,263 , GRCh38.p12 chr5: 33,948,941-33,948,941 , GRCh38.p12 chr5|NT_187551.1: 150,361-150,361 SLC45A2
    nsv5327377translocation1nstd204human GRCh38.p13 chr5: 33,968,272-33,968,272 , GRCh38.p13 chr5: 33,967,721-33,967,721 , GRCh37.p13 chr5: 33,968,377-33,968,377 , GRCh37.p13 chr5: 33,967,826-33,967,826 SLC45A2
    nsv5300787copy number variation1nstd204human GRCh38.p13 chr5: 33,943,790-33,943,932 , GRCh37.p13 chr5: 33,943,895-33,944,037 SLC45A2
    nsv4937270copy number variation1nstd200human GRCh38 chr5: 33,957,386-33,958,599 , GRCh37.p13 chr5: 33,957,491-33,958,704 SLC45A2
    nsv4937269copy number variation1nstd200human GRCh38 chr5: 33,943,800-33,943,923 , GRCh37.p13 chr5: 33,943,905-33,944,028 SLC45A2
    nsv4802474copy number variation1nstd200human GRCh37 chr5: 33,943,905-33,944,028 , GRCh38.p12 chr5: 33,943,800-33,943,923 , GRCh38.p12 chr5|NT_187551.1: 145,122-145,245 SLC45A2
    nsv4762598inversion1nstd199human GRCh37 chr5: 20,832,595-34,371,602 , GRCh38.p12 chr5: 20,832,486-34,371,497 , CDH6, 117 more genes
    nsv4751404inversion1nstd199human GRCh37 chr5: 20,834,824-34,371,606 , GRCh38.p12 chr5: 20,834,715-34,371,501 , CDH6, 117 more genes
    nsv4729129copy number variation1nstd102humanUncertain significance GRCh37 chr5: 33,501,565-34,167,822 , GRCh38.p12 chr5: 33,501,460-34,167,717 SLC45A2, ST3GAL5P1, 9 more genes
    nsv4729066copy number variation1nstd102humanUncertain significance GRCh37 chr5: 33,945,587-34,754,248 , GRCh38.p12 chr5: 33,945,482-34,754,143 RAI14-DT, C1QTNF3, 10 more genes
    nsv4724737insertion1nstd186human GRCh37 chr5: 33,975,086-33,975,086 , GRCh38.p12 chr5: 33,974,981-33,974,981 SLC45A2
    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