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Items: 1 to 20 of 272

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137693copy number variation1nstd102humannot provided GRCh38 chr2: 46,722,010-46,985,532 , GRCh37.p13 chr2: 46,949,149-47,212,671 TTC7A, LINC01119, 4 more genes
    nsv6113868mobile element insertion1nstd186human GRCh37 chr2: 46,928,953-46,929,004 , GRCh38.p12 chr2: 46,701,814-46,701,865 SOCS5
    nsv5962699insertion1nstd209human GRCh38 chr2: 46,701,811-46,701,811 , GRCh37.p13 chr2: 46,928,950-46,928,950 SOCS5
    nsv5872392copy number variation1nstd209human GRCh38 chr2: 46,751,611-46,752,174 , GRCh37.p13 chr2: 46,978,750-46,979,313 SOCS5
    nsv5691735mobile element insertion1nstd211human GRCh38 chr2: 46,712,814-46,712,814 , GRCh37.p13 chr2: 46,939,953-46,939,953 SOCS5
    nsv5689245mobile element insertion1nstd211human GRCh38 chr2: 46,738,749-46,738,749 , GRCh37.p13 chr2: 46,965,888-46,965,888 SOCS5
    nsv5685564mobile element insertion1nstd211human GRCh38 chr2: 46,746,943-46,746,943 , GRCh37.p13 chr2: 46,974,082-46,974,082 SOCS5
    nsv5684286mobile element insertion2nstd211human GRCh38 chr2: 46,701,814-46,701,814 , GRCh37.p13 chr2: 46,928,953-46,928,953 SOCS5
    nsv5619681insertion1nstd207human GRCh38 chr2: 46,701,811-46,701,811 , GRCh37.p13 chr2: 46,928,950-46,928,950 SOCS5
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5534769insertion1nstd206human GRCh38 chr2: 46,738,749-46,738,784 , GRCh37.p13 chr2: 46,965,888-46,965,923 SOCS5
    nsv5447667copy number variation1nstd206human GRCh38 chr2: 46,709,163-46,712,570 , GRCh37.p13 chr2: 46,936,302-46,939,709 SOCS5
    nsv5439891copy number variation1nstd206human GRCh38 chr2: 46,616,100-46,712,363 , GRCh37.p13 chr2: 46,843,239-46,939,502 PIGF, CRIPT, 2 more genes
    nsv5434516copy number variation1nstd206human GRCh38 chr2: 46,744,253-46,744,763 , GRCh37.p13 chr2: 46,971,392-46,971,902 SOCS5
    nsv5434090copy number variation1nstd206human GRCh38 chr2: 46,740,672-46,751,806 , GRCh37.p13 chr2: 46,967,811-46,978,945 SOCS5
    nsv5399456mobile element insertion1nstd206human GRCh38 chr2: 46,701,814-46,701,865 , GRCh37.p13 chr2: 46,928,953-46,929,004 SOCS5
    nsv5359841translocation1nstd200human GRCh38 chr2: 46,725,405-46,725,405 , GRCh38 chr2: 46,725,966-46,725,966 , GRCh37.p13 chr2: 46,952,544-46,952,544 , GRCh37.p13 chr2: 46,953,105-46,953,105 SOCS5
    nsv5294997copy number variation1nstd204human GRCh38.p13 chr2: 46,744,227-46,744,792 , GRCh37.p13 chr2: 46,971,366-46,971,931 SOCS5
    nsv5200479copy number variation1nstd204human GRCh38.p13 chr2: 46,721,101-46,725,000 , GRCh37.p13 chr2: 46,948,240-46,952,139 SOCS5
    nsv5174064mobile element insertion1nstd203human GRCh38 chr2: 46,733,650-46,733,672 , GRCh37.p13 chr2: 46,960,789-46,960,811 SOCS5
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