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 333

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926381copy number variation1nstd209human GRCh38 chr12: 32,745,695-32,745,760 , GRCh37.p13 chr12: 32,898,629-32,898,694 DNM1L, YARS2
    nsv5921442copy number variation1nstd209human GRCh38 chr12: 32,708,417-32,709,077 , GRCh37.p13 chr12: 32,861,351-32,862,011 DNM1L
    nsv5916528copy number variation1nstd209human GRCh38 chr12: 32,677,793-32,678,628 , GRCh37.p13 chr12: 32,830,727-32,831,562 DNM1L
    nsv5916046copy number variation1nstd209human GRCh38 chr12: 32,676,947-32,678,821 , GRCh37.p13 chr12: 32,829,881-32,831,755 DNM1L
    nsv5910490copy number variation1nstd209human GRCh38 chr12: 32,727,281-32,727,337 , GRCh37.p13 chr12: 32,880,215-32,880,271 DNM1L, YARS2, 1 more genes
    nsv5851611copy number variation1nstd209human GRCh38 chr12: 32,677,069-32,678,691 , GRCh37.p13 chr12: 32,830,003-32,831,625 DNM1L
    nsv5848266copy number variation1nstd209human GRCh38 chr12: 32,733,686-32,736,142 , GRCh37.p13 chr12: 32,886,620-32,889,076 DNM1L, YARS2
    nsv5656901insertion1nstd207human GRCh38 chr12: 32,717,738-32,717,738 , GRCh37.p13 chr12: 32,870,672-32,870,672 DNM1L
    nsv5603063copy number variation1nstd207human GRCh38 chr12: 32,717,571-32,717,636 , GRCh37.p13 chr12: 32,870,505-32,870,570 DNM1L
    nsv5599829copy number variation1nstd207human GRCh38 chr12: 32,717,229-32,717,637 , GRCh37.p13 chr12: 32,870,163-32,870,571 DNM1L
    nsv5597482copy number variation1nstd207human GRCh38 chr12: 32,717,340-32,717,427 , GRCh37.p13 chr12: 32,870,274-32,870,361 DNM1L
    nsv5564293copy number variation1nstd102humanUncertain significance GRCh37 chr12: 32,772,622-33,049,675 , GRCh38.p12 chr12: 32,619,688-32,896,741 PKP2, LOC100420981, 4 more genes
    nsv5562828inversion1nstd206human GRCh38 chr12: 32,724,568-32,724,709 , GRCh37.p13 chr12: 32,877,502-32,877,643 DNM1L, YARS2, 1 more genes
    nsv5549397insertion1nstd206human GRCh38 chr12: 32,722,893-32,722,921 , GRCh37.p13 chr12: 32,875,827-32,875,855 DNM1L
    nsv5509992copy number variation1nstd206human GRCh38 chr12: 32,745,696-32,745,761 , GRCh37.p13 chr12: 32,898,630-32,898,695 YARS2, DNM1L
    nsv5506171copy number variation1nstd206human GRCh38 chr12: 32,717,230-32,717,686 , GRCh37.p13 chr12: 32,870,164-32,870,620 DNM1L
    nsv5506040copy number variation1nstd206human GRCh38 chr12: 32,676,950-32,678,822 , GRCh37.p13 chr12: 32,829,884-32,831,756 DNM1L
    nsv5502357copy number variation1nstd206human GRCh38 chr12: 32,682,574-32,684,283 , GRCh37.p13 chr12: 32,835,508-32,837,217 DNM1L
    nsv5500088copy number variation1nstd206human GRCh38 chr12: 32,684,061-32,688,819 , GRCh37.p13 chr12: 32,836,995-32,841,753 DNM1L
    nsv5499062copy number variation1nstd206human GRCh38 chr12: 32,677,807-32,678,609 , GRCh37.p13 chr12: 32,830,741-32,831,543 DNM1L
    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