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 179

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066856inversion1nstd229human GRCh38 chr14: 74,700,665-74,838,594 , GRCh37.p13 chr14: 75,167,368-75,305,297 AREL1, YLPM1, 2 more genes
    nsv6975857copy number variation1nstd229human GRCh38 chr14: 74,502,780-74,690,439 , GRCh37.p13 chr14: 74,969,483-75,157,142 LOC101928352, LTBP2, 3 more genes
    nsv6971978copy number variation1nstd229human GRCh38 chr14: 74,701,312-74,706,911 , GRCh37.p13 chr14: 75,168,015-75,173,614 AREL1
    nsv6965696copy number variation1nstd229human GRCh38 chr14: 74,476,001-74,700,700 , GRCh37.p13 chr14: 74,942,704-75,167,403 ISCA2, RAP1AP, 8 more genes
    nsv6594541inversion1nstd223human GRCh38 chr14: 74,691,011-74,692,719 , GRCh37.p13 chr14: 75,157,714-75,159,422 AREL1
    nsv6590450inversion1nstd223human GRCh38 chr14: 74,691,138-74,692,607 , GRCh37.p13 chr14: 75,157,841-75,159,310 AREL1
    nsv6577694inversion1nstd223human GRCh38 chr14: 74,694,776-74,695,305 , GRCh37.p13 chr14: 75,161,479-75,162,008 AREL1
    nsv6494757copy number variation1nstd223human GRCh38 chr14: 74,679,914-74,681,512 , GRCh37.p13 chr14: 75,146,617-75,148,215 AREL1
    nsv6491559copy number variation1nstd223human GRCh38 chr14: 74,636,726-74,689,938 , GRCh37.p13 chr14: 75,103,429-75,156,641 LOC100419503, AREL1, 1 more genes
    nsv6487714copy number variation1nstd223human GRCh38 chr14: 74,701,308-74,706,910 , GRCh37.p13 chr14: 75,168,011-75,173,613 AREL1
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6241523mobile element insertion1nstd215human GRCh38 chr14: 74,712,077-74,712,077 , GRCh37.p13 chr14: 75,178,780-75,178,780 FCF1, AREL1
    nsv6204893copy number variation1nstd214human GRCh38 chr14: 74,707,748-74,707,910 , GRCh37.p13 chr14: 75,174,451-75,174,613 AREL1
    nsv6187747copy number variation1nstd214human GRCh38 chr14: 74,707,719-74,707,881 , GRCh37.p13 chr14: 75,174,422-75,174,584 AREL1
    nsv6132792copy number variation1nstd213human GRCh37 chr14: 74,650,000-75,390,001 , GRCh38.p12 chr14: 74,183,297-74,923,298 AREL1, NPC2, 23 more genes
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 ACTN1, ACYP1, 400 more genes
    nsv5712413mobile element insertion1nstd211human GRCh38 chr14: 74,712,077-74,712,077 , GRCh37.p13 chr14: 75,178,780-75,178,780 FCF1, AREL1
    nsv5711002mobile element insertion1nstd211human GRCh38 chr14: 74,705,598-74,705,598 , GRCh37.p13 chr14: 75,172,301-75,172,301 AREL1
    nsv5707325mobile element insertion1nstd211human GRCh38 chr14: 74,705,609-74,705,609 , GRCh37.p13 chr14: 75,172,312-75,172,312 AREL1
    nsv5704016mobile element insertion2nstd211human GRCh38 chr14: 74,666,650-74,666,650 , GRCh37.p13 chr14: 75,133,353-75,133,353 AREL1
    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