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  • The following term was not found in dbVar: 4826193.
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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3885087copy number variation1nstd102humanBenign GRCh37 chr3: 118,731,305-118,824,418 , GRCh38.p12 chr3: 119,012,458-119,105,571 IGSF11
    nsv3921471copy number variation1nstd102humanLikely benign NCBI36 chr3: 120,217,976-120,300,418 , GRCh37 chr3: 118,735,286-118,817,728 , GRCh38 chr3: 119,016,439-119,098,881 IGSF11
    nsv3876837copy number variation1nstd102humanBenign GRCh37 chr3: 118,730,933-118,812,889 , GRCh38.p12 chr3: 119,012,086-119,094,042 IGSF11
    nsv3913744copy number variation1nstd102humanBenign/Likely benign GRCh38 chr3: 119,033,541-119,081,373 , GRCh37 chr3: 118,752,388-118,800,220 , NCBI36 chr3: 120,235,078-120,282,910 IGSF11
    nsv3921091copy number variation1nstd102humanBenign/Likely benign GRCh37 chr3: 118,778,681-118,800,220 , NCBI36 chr3: 120,261,371-120,282,910 , GRCh38 chr3: 119,059,834-119,081,373 IGSF11
    esv3995793copy number variation1estd218human GRCh37 chr3: 118,742,848-118,760,722 , GRCh38.p12 chr3: 119,024,001-119,041,875 IGSF11
    nsv6709474copy number variation1nstd229human GRCh38 chr3: 119,044,019-119,101,631 , GRCh37.p13 chr3: 118,762,866-118,820,478 IGSF11
    nsv6716629copy number variation1nstd229human GRCh38 chr3: 119,084,501-119,137,800 , GRCh37.p13 chr3: 118,803,348-118,856,647 IGSF11
    nsv6701521copy number variation1nstd229human GRCh38 chr3: 118,972,493-118,997,511 , GRCh37.p13 chr3: 118,691,340-118,716,358 IGSF11
    nsv6702951copy number variation1nstd229human GRCh38 chr3: 119,075,621-119,086,870 , GRCh37.p13 chr3: 118,794,468-118,805,717 IGSF11
    nsv6711612copy number variation1nstd229human GRCh38 chr3: 119,045,169-119,055,592 , GRCh37.p13 chr3: 118,764,016-118,774,439 IGSF11
    nsv6706482copy number variation1nstd229human GRCh38 chr3: 118,919,201-118,924,500 , GRCh37.p13 chr3: 118,638,048-118,643,347 IGSF11
    nsv6714654copy number variation1nstd229human GRCh38 chr3: 118,987,496-118,991,495 , GRCh37.p13 chr3: 118,706,343-118,710,342 IGSF11
    nsv6713137copy number variation1nstd229human GRCh38 chr3: 119,124,953-119,128,530 , GRCh37.p13 chr3: 118,843,800-118,847,377 IGSF11
    nsv6698998copy number variation1nstd229human GRCh38 chr3: 119,063,300-119,066,856 , GRCh37.p13 chr3: 118,782,147-118,785,703 IGSF11
    nsv6708943copy number variation1nstd229human GRCh38 chr3: 118,950,540-118,954,038 , GRCh37.p13 chr3: 118,669,387-118,672,885 IGSF11
    nsv6709102copy number variation1nstd229human GRCh38 chr3: 118,905,786-118,908,661 , GRCh37.p13 chr3: 118,624,633-118,627,508 IGSF11
    nsv6698528copy number variation1nstd229human GRCh38 chr3: 118,951,906-118,954,490 , GRCh37.p13 chr3: 118,670,753-118,673,337 IGSF11
    nsv6713423copy number variation1nstd229human GRCh38 chr3: 119,104,063-119,104,113 , GRCh37.p13 chr3: 118,822,910-118,822,960 IGSF11
    nsv6714043copy number variation1nstd229human GRCh38 chr3: 119,140,836-119,140,878 , GRCh37.p13 chr3: 118,859,683-118,859,725 IGSF11
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