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 98

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5888462copy number variation1nstd209human GRCh38 chr5: 56,121,599-56,123,843 , GRCh37.p13 chr5: 55,417,426-55,419,670 ANKRD55, LOC101928419, 1 more genes
    nsv5843094copy number variation1nstd209human GRCh38 chr5: 56,122,775-56,123,974 , GRCh37.p13 chr5: 55,418,602-55,419,801 ANKRD55, RNU6-299P, 1 more genes
    nsv5842805copy number variation1nstd209human GRCh38 chr5: 56,121,525-56,123,924 , GRCh37.p13 chr5: 55,417,352-55,419,751 ANKRD55, RNU6-299P, 1 more genes
    nsv5564868copy number variation1nstd207human GRCh38 chr5: 56,123,034-56,124,640 , GRCh37.p13 chr5: 55,418,861-55,420,467 ANKRD55, LOC101928419, 1 more genes
    nsv5463486copy number variation1nstd206human GRCh38 chr5: 56,122,783-56,124,641 , GRCh37.p13 chr5: 55,418,610-55,420,468 LOC101928419, RNU6-299P, 1 more genes
    nsv4931614copy number variation1nstd200human GRCh38 chr5: 56,121,630-56,122,447 , GRCh37.p13 chr5: 55,417,457-55,418,274 LOC101928419, ANKRD55
    nsv4662876copy number variation1nstd186human GRCh37 chr5: 55,418,521-55,420,121 , GRCh38.p12 chr5: 56,122,694-56,124,294 ANKRD55, LOC101928419, 1 more genes
    nsv4598164copy number variation1nstd183human GRCh37 chr5: 55,418,529-55,420,121 , GRCh38.p12 chr5: 56,122,702-56,124,294 RNU6-299P, ANKRD55, 1 more genes
    nsv4598163copy number variation1nstd183human GRCh37 chr5: 55,418,521-55,420,121 , GRCh38.p12 chr5: 56,122,694-56,124,294 RNU6-299P, LOC101928419, 1 more genes
    nsv4492257mobile element insertion1nstd166human GRCh37.p13 chr5: 55,421,609-55,421,609 , GRCh38.p12 chr5: 56,125,782-56,125,782 ANKRD55, LOC101928419, 1 more genes
    nsv4481482mobile element insertion1nstd166human GRCh37.p13 chr5: 55,420,937-55,420,937 , GRCh38.p12 chr5: 56,125,110-56,125,110 ANKRD55, LOC101928419, 1 more genes
    nsv4456103copy number variation1nstd102humanUncertain significance GRCh37 chr5: 54,527,018-55,436,536 , GRCh38.p12 chr5: 55,231,190-56,140,709 HNRNPH1P3, DDX4, 20 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4131273copy number variation1nstd166human GRCh37.p13 chr5: 55,418,610-55,420,468 , GRCh38.p12 chr5: 56,122,783-56,124,641 ANKRD55, RNU6-299P, 1 more genes
    nsv4119813copy number variation1nstd166human GRCh37.p13 chr5: 39,131,458-67,637,618 , GRCh38.p12 chr5: 39,131,356-68,341,790 , ESM1, 305 more genes
    nsv3961436copy number variation1nstd168human GRCh38 chr5: 56,115,690-56,144,865 , GRCh37.p13 chr5: 55,411,517-55,440,692 RNU6-299P, ANKRD55, 3 more genes
    nsv3923429copy number variation1nstd102humanPathogenic GRCh37 chr5: 49,584,189-62,445,597 , NCBI36 chr5: 49,619,946-62,481,353 , GRCh38 chr5: 50,288,355-63,149,770 ISCA1P1, LOC643307, 163 more genes
    nsv3920391copy number variation1nstd102humanPathogenic GRCh38 chr5: 35,201,559-61,903,141 , GRCh37 chr5: 35,201,661-61,198,968 , NCBI36 chr5: 35,237,418-61,234,725 KRT18P56, LINC01265, 290 more genes
    nsv3913817copy number variation1nstd102humanUncertain significance GRCh37 chr5: 45,566,963-55,802,320 , GRCh38 chr5: 45,566,861-56,506,493 , NCBI36 chr5: 45,602,720-55,838,077 LINC02118, ARL15, 90 more genes
    nsv3912593copy number variation1nstd102humanUncertain significance NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259 LOC105378993, LOC107986375, 2492 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