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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960709insertion1nstd209human GRCh38 chr1: 167,483,016-167,483,016 , GRCh37.p13 chr1: 167,452,253-167,452,253 CD247
    nsv5947784insertion1nstd209human GRCh38 chr1: 167,453,037-167,453,037 , GRCh37.p13 chr1: 167,422,274-167,422,274 CD247, LOC101928512
    nsv5881291copy number variation1nstd209human GRCh38 chr1: 167,468,294-167,470,310 , GRCh37.p13 chr1: 167,437,531-167,439,547 CD247
    nsv5878981copy number variation1nstd209human GRCh38 chr1: 167,427,843-167,428,811 , GRCh37.p13 chr1: 167,397,080-167,398,048 POU2F1, CD247
    nsv5828522copy number variation1nstd209human GRCh38 chr1: 167,468,435-167,470,334 , GRCh37.p13 chr1: 167,437,672-167,439,571 CD247
    nsv5678965mobile element insertion1nstd211human GRCh38 chr1: 167,470,527-167,470,527 , GRCh37.p13 chr1: 167,439,764-167,439,764 CD247
    nsv5621901insertion1nstd207human GRCh38 chr1: 167,435,083-167,435,083 , GRCh37.p13 chr1: 167,404,320-167,404,320 CD247
    nsv5621037insertion1nstd207human GRCh38 chr1: 167,434,947-167,434,947 , GRCh37.p13 chr1: 167,404,184-167,404,184 CD247
    nsv5619392insertion1nstd207human GRCh38 chr1: 167,434,959-167,434,959 , GRCh37.p13 chr1: 167,404,196-167,404,196 CD247
    nsv5619023insertion1nstd207human GRCh38 chr1: 167,483,013-167,483,013 , GRCh37.p13 chr1: 167,452,250-167,452,250 CD247
    nsv5612784insertion1nstd207human GRCh38 chr1: 167,435,206-167,435,206 , GRCh37.p13 chr1: 167,404,443-167,404,443 CD247
    nsv5606286insertion1nstd207human GRCh38 chr1: 167,435,070-167,435,070 , GRCh37.p13 chr1: 167,404,307-167,404,307 CD247
    nsv5572559copy number variation1nstd207human GRCh38 chr1: 167,434,903-167,434,964 , GRCh37.p13 chr1: 167,404,140-167,404,201 CD247
    nsv5564406copy number variation1nstd102humanUncertain significance GRCh37 chr1: 167,400,898-167,487,722 , GRCh38.p12 chr1: 167,431,661-167,518,485 LOC101928512, CD247, 1 more genes
    nsv5426967copy number variation1nstd206human GRCh38 chr1: 167,428,745-167,430,874 , GRCh37.p13 chr1: 167,397,982-167,400,111 CD247
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5379074translocation1nstd200human GRCh38 chr1: 167,478,857-167,478,857 , GRCh38 chr1: 167,506,125-167,506,125 , GRCh37.p13 chr1: 167,475,362-167,475,362 , GRCh37.p13 chr1: 167,448,094-167,448,094 CD247
    nsv5379069translocation1nstd200human GRCh38 chr1: 167,504,188-167,504,188 , GRCh38 chr1: 167,459,751-167,459,751 , GRCh37.p13 chr1: 167,473,425-167,473,425 , GRCh37.p13 chr1: 167,428,988-167,428,988 CD247
    nsv5075313mobile element insertion1nstd203human GRCh38 chr1: 167,513,959-167,513,971 , GRCh37.p13 chr1: 167,483,196-167,483,208 CD247
    nsv5073592mobile element insertion1nstd203human GRCh38 chr1: 167,506,245-167,506,245 , GRCh37.p13 chr1: 167,475,482-167,475,482 CD247
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