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 490

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075613inversion1nstd229human GRCh38 chr8: 64,616,948-64,616,969 , GRCh37.p13 chr8: 65,529,505-65,529,526 CYP7B1
    nsv7070230inversion1nstd229human GRCh38 chr8: 64,634,122-64,717,397 , GRCh37.p13 chr8: 65,546,679-65,629,954 CYP7B1
    nsv7066592inversion1nstd229human GRCh38 chr8: 64,627,706-64,716,383 , GRCh37.p13 chr8: 65,540,263-65,628,940 CYP7B1
    nsv7062610inversion1nstd229human GRCh38 chr8: 60,977,244-66,075,546 , GRCh37.p13 chr8: 61,889,803-66,987,781 LOC105375870, LINC01289, 55 more genes
    nsv6858023copy number variation1nstd229human GRCh38 chr8: 64,725,652-64,734,596 , GRCh37.p13 chr8: 65,638,209-65,647,153 CYP7B1
    nsv6856655copy number variation1nstd229human GRCh38 chr8: 64,667,954-64,673,089 , GRCh37.p13 chr8: 65,580,511-65,585,646 CYP7B1
    nsv6855885copy number variation1nstd229human GRCh38 chr8: 64,648,363-64,657,168 , GRCh37.p13 chr8: 65,560,920-65,569,725 CYP7B1
    nsv6853992copy number variation1nstd229human GRCh38 chr8: 64,625,377-64,626,630 , GRCh37.p13 chr8: 65,537,934-65,539,187 CYP7B1
    nsv6853341copy number variation1nstd229human GRCh38 chr8: 64,648,660-64,649,995 , GRCh37.p13 chr8: 65,561,217-65,562,552 CYP7B1
    nsv6853017copy number variation1nstd229human GRCh38 chr8: 64,690,448-64,690,894 , GRCh37.p13 chr8: 65,603,005-65,603,451 CYP7B1
    nsv6852611copy number variation1nstd229human GRCh38 chr8: 64,552,298-65,913,335 , GRCh37.p13 chr8: 65,464,855-66,825,570 LOC105375880, PDE7A, 14 more genes
    nsv6852273copy number variation1nstd229human GRCh38 chr8: 61,996,129-66,319,713 , GRCh37.p13 chr8: 62,908,688-67,231,948 LOC112268028, LOC105375873, 52 more genes
    nsv6850825copy number variation1nstd229human GRCh38 chr8: 64,623,591-64,631,870 , GRCh37.p13 chr8: 65,536,148-65,544,427 CYP7B1
    nsv6850319copy number variation1nstd229human GRCh38 chr8: 64,700,453-64,702,762 , GRCh37.p13 chr8: 65,613,010-65,615,319 CYP7B1
    nsv6846991copy number variation1nstd229human GRCh38 chr8: 64,663,501-64,667,100 , GRCh37.p13 chr8: 65,576,058-65,579,657 CYP7B1
    nsv6846293copy number variation1nstd229human GRCh38 chr8: 64,642,114-64,652,529 , GRCh37.p13 chr8: 65,554,671-65,565,086 CYP7B1
    nsv6846146copy number variation1nstd229human GRCh38 chr8: 64,795,253-64,795,461 , GRCh37.p13 chr8: 65,707,810-65,708,018 CYP7B1
    nsv6844391copy number variation1nstd229human GRCh38 chr8: 64,677,872-64,683,034 , GRCh37.p13 chr8: 65,590,429-65,595,591 CYP7B1
    nsv6843973copy number variation1nstd229human GRCh38 chr8: 64,640,742-64,643,770 , GRCh37.p13 chr8: 65,553,299-65,556,327 CYP7B1
    nsv6843369copy number variation1nstd229human GRCh38 chr8: 64,742,182-64,742,255 , GRCh37.p13 chr8: 65,654,739-65,654,812 CYP7B1
    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