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 227

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075711inversion1nstd229human GRCh38 chr8: 102,102,164-111,409,427 , GRCh37.p13 chr8: 103,114,392-112,421,656 LINC01181, LOC105375690, 118 more genes
    nsv7072523inversion1nstd229human GRCh38 chr8: 109,174,100-109,681,746 , GRCh37.p13 chr8: 110,186,329-110,693,975 EBAG9, SYBU, 6 more genes
    nsv6855990copy number variation1nstd229human GRCh38 chr8: 109,541,203-109,541,328 , GRCh37.p13 chr8: 110,553,432-110,553,557 EBAG9
    nsv6855123copy number variation1nstd229human GRCh38 chr8: 108,779,510-109,673,989 , GRCh37.p13 chr8: 109,791,739-110,686,218 NUDCD1, EBAG9, 10 more genes
    nsv6853404copy number variation1nstd229human GRCh38 chr8: 109,540,616-110,058,754 , GRCh37.p13 chr8: 110,552,845-111,070,983 SYBU, EBAG9, 4 more genes
    nsv6845855copy number variation1nstd229human GRCh38 chr8: 109,539,659-109,607,408 , GRCh37.p13 chr8: 110,551,888-110,619,637 EBAG9, SYBU
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6570439inversion1nstd223human GRCh38 chr8: 109,545,174-109,545,670 , GRCh37.p13 chr8: 110,557,403-110,557,899 EBAG9
    nsv6556180inversion1nstd223human GRCh38 chr8: 109,374,224-111,632,454 , GRCh37.p13 chr8: 110,386,453-112,644,683 H2AZP7, LOC644335, 21 more genes
    nsv6434556copy number variation1nstd223human GRCh38 chr8: 109,548,201-109,550,100 , GRCh37.p13 chr8: 110,560,430-110,562,329 EBAG9
    nsv6434426copy number variation1nstd223human GRCh38 chr8: 109,549,748-109,550,248 , GRCh37.p13 chr8: 110,561,977-110,562,477 EBAG9
    nsv6427835copy number variation1nstd223human GRCh38 chr8: 109,548,496-109,549,003 , GRCh37.p13 chr8: 110,560,725-110,561,232 EBAG9
    nsv6421994copy number variation1nstd223human GRCh38 chr8: 109,565,901-109,566,900 , GRCh37.p13 chr8: 110,578,130-110,579,129 EBAG9
    nsv6419983copy number variation1nstd223human GRCh38 chr8: 109,482,094-109,564,342 , GRCh37.p13 chr8: 110,494,323-110,576,571 PKHD1L1, EBAG9
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
    nsv6314744copy number variation1nstd102humanPathogenic GRCh37 chr8: 96,496,503-146,295,711 , GRCh38.p12 chr8: 95,484,275-145,070,325 OSR2, LOC392268, 676 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6136605copy number variation1nstd213human GRCh37 chr8: 86,730,000-120,700,001 , GRCh38.p12 chr8: 85,717,771-119,687,761 CALB1, CDH17, 421 more genes
    nsv6136300copy number variation1nstd213human GRCh37 chr8: 107,740,000-120,740,001 , GRCh38.p12 chr8: 106,727,772-119,727,761 EXT1, CCN3, 107 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