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 189

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5688095mobile element insertion2nstd211human GRCh38 chr3: 167,446,548-167,446,548 , GRCh37.p13 chr3: 167,164,336-167,164,336 SERPINI2
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5438509copy number variation1nstd206human GRCh38 chr3: 167,445,691-167,446,487 , GRCh37.p13 chr3: 167,163,479-167,164,275 SERPINI2
    nsv5437627copy number variation1nstd206human GRCh38 chr3: 167,446,066-167,446,492 , GRCh37.p13 chr3: 167,163,854-167,164,280 SERPINI2
    nsv5394767mobile element insertion1nstd206human GRCh38 chr3: 167,446,548-167,446,566 , GRCh37.p13 chr3: 167,164,336-167,164,354 SERPINI2
    nsv5352152translocation1nstd200human GRCh38 chr3: 167,448,973-167,448,973 , GRCh38 chr3: 167,448,869-167,448,869 , GRCh37.p13 chr3: 167,166,657-167,166,657 , GRCh37.p13 chr3: 167,166,761-167,166,761 SERPINI2
    nsv5228629copy number variation1nstd204human GRCh38.p13 chr3: 167,471,101-167,475,200 , GRCh37.p13 chr3: 167,188,889-167,192,988 LOC105374197, SERPINI2
    nsv5084881mobile element insertion1nstd203human GRCh38 chr3: 167,452,755-167,452,766 , GRCh37.p13 chr3: 167,170,543-167,170,554 SERPINI2
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4804975copy number variation1nstd200human GRCh37 chr3: 167,172,945-167,185,928 , GRCh38.p12 chr3: 167,455,157-167,468,140 SERPINI2, LOC105374197
    nsv4728207copy number variation1nstd102humanUncertain significance GRCh37 chr3: 166,831,213-167,390,123 , GRCh38.p12 chr3: 167,113,425-167,672,335 WDR49, LOC105374197, 3 more genes
    nsv4674443copy number variation1nstd102humanUncertain significance GRCh37 chr3: 167,187,409-167,318,904 , GRCh38.p12 chr3: 167,469,621-167,601,116 LOC105374197, SERPINI2, 1 more genes
    nsv4585566copy number variation1nstd183human GRCh37 chr3: 166,785,340-167,379,233 , GRCh38.p12 chr3: 167,067,552-167,661,445 SERPINI2, ZBBX, 4 more genes
    nsv4585217copy number variation1nstd183human GRCh37 chr3: 167,191,537-167,197,021 , GRCh38.p12 chr3: 167,473,749-167,479,233 WDR49, SERPINI2, 1 more genes
    nsv4585214copy number variation1nstd183human GRCh37 chr3: 166,783,403-167,371,989 , GRCh38.p12 chr3: 167,065,615-167,654,201 SERPINI2, ZBBX, 5 more genes
    nsv4470228mobile element insertion1nstd166human GRCh37.p13 chr3: 167,164,319-167,164,319 , GRCh38.p12 chr3: 167,446,531-167,446,531 SERPINI2
    nsv4469597mobile element insertion1nstd166human GRCh37.p13 chr3: 167,170,543-167,170,543 , GRCh38.p12 chr3: 167,452,755-167,452,755 SERPINI2
    nsv4452794copy number variation1nstd102humanPathogenic GRCh37 chr3: 165,603,872-168,796,960 , GRCh38.p12 chr3: 165,886,084-169,079,172 MTND4P17, LINC02082, 31 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4112041copy number variation1nstd166human GRCh37.p13 chr3: 167,184,173-167,184,723 , GRCh38.p12 chr3: 167,466,385-167,466,935 LOC105374197, SERPINI2
    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