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 1373

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148134copy number variation1nstd102humanPathogenic GRCh37 chr8: 61,121,294-63,502,403 , GRCh38.p12 chr8: 60,208,735-62,589,844 LOC112268028, LOC105375864, 23 more genes
    nsv7144439insertion1nstd232human GRCh37.p13 chr8: 62,119,936-62,119,936 , GRCh38.p12 chr8: 61,207,377-61,207,377 CLVS1
    nsv7143450copy number variation1nstd232human GRCh37.p13 chr8: 62,155,493-62,155,547 , GRCh38.p12 chr8: 61,242,934-61,242,988 CLVS1
    nsv7140924insertion1nstd232human GRCh37.p13 chr8: 62,087,432-62,087,432 , GRCh38.p12 chr8: 61,174,873-61,174,873 CLVS1
    nsv7077722inversion1nstd229human GRCh38 chr8: 61,326,985-61,335,482 , GRCh37.p13 chr8: 62,239,544-62,248,041 CLVS1
    nsv7075533inversion1nstd229human GRCh38 chr8: 60,979,469-60,980,778 , GRCh37.p13 chr8: 61,892,028-61,893,337 CLVS1
    nsv7072965inversion1nstd229human GRCh38 chr8: 61,278,346-61,278,363 , GRCh37.p13 chr8: 62,190,905-62,190,922 CLVS1
    nsv7071967inversion1nstd229human GRCh38 chr8: 61,327,160-61,330,023 , GRCh37.p13 chr8: 62,239,719-62,242,582 CLVS1
    nsv7070051inversion1nstd229human GRCh38 chr8: 61,330,031-61,335,478 , GRCh37.p13 chr8: 62,242,590-62,248,037 CLVS1
    nsv7069431inversion1nstd229human GRCh38 chr8: 60,974,241-60,974,280 , GRCh37.p13 chr8: 61,886,800-61,886,839 CLVS1
    nsv7067845inversion1nstd229human GRCh38 chr8: 61,266,145-61,266,231 , GRCh37.p13 chr8: 62,178,704-62,178,790 CLVS1
    nsv7066620inversion1nstd229human GRCh38 chr8: 61,453,413-61,453,527 , GRCh37.p13 chr8: 62,365,972-62,366,086 CLVS1
    nsv7062610inversion1nstd229human GRCh38 chr8: 60,977,244-66,075,546 , GRCh37.p13 chr8: 61,889,803-66,987,781 LOC105375870, LINC01289, 55 more genes
    nsv7061230inversion1nstd229human GRCh38 chr8: 61,311,056-61,611,540 , GRCh37.p13 chr8: 62,223,615-62,524,099 CLVS1, ASPH, 2 more genes
    nsv7060660inversion1nstd229human GRCh38 chr8: 61,330,495-61,400,132 , GRCh37.p13 chr8: 62,243,054-62,312,691 LOC105375870, CLVS1
    nsv7060191inversion1nstd229human GRCh38 chr8: 61,101,089-61,101,226 , GRCh37.p13 chr8: 62,013,648-62,013,785 CLVS1
    nsv7059036inversion1nstd229human GRCh38 chr8: 61,373,477-61,423,758 , GRCh37.p13 chr8: 62,286,036-62,336,317 LOC105375870, CLVS1
    nsv6857871copy number variation1nstd229human GRCh38 chr8: 61,069,520-61,082,208 , GRCh37.p13 chr8: 61,982,079-61,994,767 CLVS1
    nsv6857827copy number variation1nstd229human GRCh38 chr8: 61,263,997-61,264,329 , GRCh37.p13 chr8: 62,176,556-62,176,888 CLVS1
    nsv6857722copy number variation1nstd229human GRCh38 chr8: 61,365,001-61,371,400 , GRCh37.p13 chr8: 62,277,560-62,283,959 LOC105375870, CLVS1
    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