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 138

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072502inversion1nstd229human GRCh38 chr8: 63,779,608-64,100,647 , GRCh37.p13 chr8: 64,692,165-65,013,204 LINC01414, LINC01289
    nsv7062610inversion1nstd229human GRCh38 chr8: 60,977,244-66,075,546 , GRCh37.p13 chr8: 61,889,803-66,987,781 LOC105375870, LINC01289, 55 more genes
    nsv6855245copy number variation1nstd229human GRCh38 chr8: 63,768,068-63,783,927 , GRCh37.p13 chr8: 64,680,626-64,696,484 LINC01289
    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
    nsv6850109copy number variation1nstd229human GRCh38 chr8: 63,757,262-63,809,176 , GRCh37.p13 chr8: 64,669,820-64,721,733 LINC01289
    nsv6636356copy number variation1nstd102humanUncertain significance GRCh37 chr8: 64,049,070-66,671,663 , GRCh38.p12 chr8: 63,136,511-65,759,428 LOC107986949, LOC107986878, 31 more genes
    nsv6431598copy number variation1nstd223human GRCh38 chr8: 63,768,068-63,783,927 , GRCh37.p13 chr8: 64,680,626-64,696,484 LINC01289
    nsv6136690copy number variation1nstd213human GRCh37 chr8: 64,070,000-66,540,001 , GRCh38.p12 chr8: 63,157,441-65,627,766 ARMC1, LINC01289, 27 more genes
    nsv6136681copy number variation1nstd213human GRCh37 chr8: 46,860,000-86,550,001 , GRCh38.p12 chr8: 45,948,378-85,637,772 CEBPD, EYA1, 519 more genes
    nsv5492348copy number variation1nstd206human GRCh38 chr8: 63,768,068-63,783,927 , GRCh37.p13 chr8: 64,680,626-64,696,484 LINC01289
    nsv5479121copy number variation1nstd206human GRCh38 chr8: 63,784,958-63,786,756 , GRCh37.p13 chr8: 64,697,515-64,699,313 LINC01289
    nsv5109472mobile element insertion1nstd203human GRCh38 chr8: 63,781,885-63,781,901 , GRCh37.p13 chr8: 64,694,442-64,694,458 LINC01289
    nsv4829053copy number variation1nstd200human GRCh37 chr8: 64,680,626-64,696,484 , GRCh38.p12 chr8: 63,768,068-63,783,927 LINC01289
    nsv4671109copy number variation1nstd186human GRCh37 chr8: 64,697,527-64,699,315 , GRCh38.p12 chr8: 63,784,970-63,786,758 LINC01289
    nsv4617822copy number variation1nstd183human GRCh37 chr8: 64,691,722-64,700,876 , GRCh38.p12 chr8: 63,779,165-63,788,319 LINC01289
    nsv4599724copy number variation1nstd183human GRCh37 chr8: 64,697,527-64,699,315 , GRCh38.p12 chr8: 63,784,970-63,786,758 LINC01289
    nsv4526969copy number variation1nstd166human GRCh37.p13 chr8: 64,681,000-64,686,000 , GRCh38.p12 chr8: 63,768,442-63,773,442 LINC01289
    nsv4485864mobile element insertion1nstd166human GRCh37.p13 chr8: 64,694,442-64,694,442 , GRCh38.p12 chr8: 63,781,885-63,781,885 LINC01289
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4395632copy number variation1nstd174human GRCh37 chr8: 64,697,505-64,699,348 , GRCh38.p12 chr8: 63,784,948-63,786,791 LINC01289
    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