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 165

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097202copy number variation1nstd102humanUncertain significance GRCh37 chr3: 49,866,536-50,540,854 , GRCh38.p12 chr3: 49,829,103-50,503,423 HYAL2, MON1A, 32 more genes
    nsv7051530inversion1nstd229human GRCh38 chr3: 49,923,418-49,923,634 , GRCh37.p13 chr3: 49,960,851-49,961,067 MON1A
    nsv6717571copy number variation1nstd229human GRCh38 chr3: 49,922,963-49,926,714 , GRCh37.p13 chr3: 49,960,396-49,964,147 MON1A
    nsv6704788copy number variation1nstd229human GRCh38 chr3: 49,918,932-49,923,260 , GRCh37.p13 chr3: 49,956,365-49,960,693 MON1A
    nsv6700836copy number variation1nstd229human GRCh38 chr3: 48,056,801-51,204,000 , GRCh37.p13 chr3: 48,098,291-51,241,431 APEH, SLC26A6, 129 more genes
    nsv6549297inversion1nstd223human GRCh38 chr3: 49,921,529-49,922,305 , GRCh37.p13 chr3: 49,958,962-49,959,738 MON1A
    nsv6357694copy number variation1nstd223human GRCh38 chr3: 49,881,227-49,921,259 , GRCh37.p13 chr3: 49,918,660-49,958,692 MON1A, MST1R
    nsv6356292copy number variation1nstd223human GRCh38 chr3: 49,905,284-49,920,604 , GRCh37.p13 chr3: 49,942,717-49,958,037 MON1A
    nsv6311990copy number variation1nstd102humanPathogenic GRCh37 chr3: 49,547,968-50,685,477 , GRCh38.p12 chr3: 49,510,535-50,648,046 APEH, RNA5SP131, 52 more genes
    nsv6277770insertion1nstd214human GRCh38 chr3: 49,911,201-49,911,201 , GRCh37.p13 chr3: 49,948,634-49,948,634 , MON1A
    nsv6253991mobile element insertion1nstd215human GRCh38 chr3: 49,929,692-49,929,692 , GRCh37.p13 chr3: 49,967,125-49,967,125 MON1A
    nsv6221234insertion1nstd214human GRCh38 chr3: 49,911,205-49,911,205 , GRCh37.p13 chr3: 49,948,638-49,948,638 , MON1A
    nsv6135016copy number variation1nstd213human GRCh37 chr3: 48,760,000-52,290,001 , GRCh38.p12 chr3: 48,722,567-52,255,985 ACY1, ALAS1, 128 more genes
    nsv6134694copy number variation1nstd213human GRCh37 chr3: 46,170,000-52,140,001 , GRCh38.p12 chr3: 46,128,508-52,105,985 ACY1, AMT, 210 more genes
    nsv6069378insertion1nstd212human GRCh38 chr3: 49,911,210-49,911,210 , GRCh37.p13 chr3: 49,948,643-49,948,643 , MON1A
    nsv6065249insertion1nstd212human GRCh38 chr3: 49,913,643-49,913,643 , GRCh37.p13 chr3: 49,951,076-49,951,076 , MON1A
    nsv5979557inversion1nstd209human GRCh37.p13 chr3: 49,958,962-49,959,737 , GRCh38 chr3: 49,921,529-49,922,304 , MON1A
    nsv5961605insertion1nstd209human GRCh38 chr3: 49,911,205-49,911,205 , GRCh37.p13 chr3: 49,948,638-49,948,638 , MON1A
    nsv5950881insertion1nstd209human GRCh38 chr3: 49,913,640-49,913,640 , GRCh37.p13 chr3: 49,951,073-49,951,073 , MON1A
    nsv5891025copy number variation1nstd209human GRCh38 chr3: 49,693,626-52,462,904 , GRCh37.p13 chr3: 49,731,059-52,496,920 , SEMA3G, 106 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