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Items: 1 to 20 of 252

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7067004inversion1nstd229human GRCh38 chr12: 106,853,473-107,177,792 , GRCh37.p13 chr12: 107,247,251-107,571,570 CRY1, TMEM263, 5 more genes
    nsv6936859copy number variation1nstd229human GRCh38 chr12: 106,775,286-106,775,402 , GRCh37.p13 chr12: 107,169,064-107,169,180 LOC100287944, RIC8B
    nsv6936797copy number variation1nstd229human GRCh38 chr12: 106,802,589-106,814,611 , GRCh37.p13 chr12: 107,196,367-107,208,389 RIC8B
    nsv6934528copy number variation1nstd229human GRCh38 chr12: 106,792,647-106,794,252 , GRCh37.p13 chr12: 107,186,425-107,188,030 RIC8B
    nsv6929574copy number variation1nstd229human GRCh38 chr12: 106,824,370-106,825,230 , GRCh37.p13 chr12: 107,218,148-107,219,008 RIC8B
    nsv6929124copy number variation1nstd229human GRCh38 chr12: 106,860,963-106,860,994 , GRCh37.p13 chr12: 107,254,741-107,254,772 RIC8B
    nsv6926598copy number variation1nstd229human GRCh38 chr12: 106,818,474-106,818,806 , GRCh37.p13 chr12: 107,212,252-107,212,584 RIC8B
    nsv6925111copy number variation1nstd229human GRCh38 chr12: 106,869,219-106,869,317 , GRCh37.p13 chr12: 107,262,997-107,263,095 LOC105369961, RIC8B
    nsv6923404copy number variation1nstd229human GRCh38 chr12: 106,871,915-106,872,239 , GRCh37.p13 chr12: 107,265,693-107,266,017 LOC105369961, RIC8B
    nsv6594203inversion1nstd223human GRCh38 chr12: 106,817,661-106,818,168 , GRCh37.p13 chr12: 107,211,439-107,211,946 RIC8B
    nsv6581221inversion1nstd223human GRCh38 chr12: 106,806,015-106,806,543 , GRCh37.p13 chr12: 107,199,793-107,200,321 RIC8B
    nsv6580022inversion1nstd223human GRCh38 chr12: 106,837,373-106,837,661 , GRCh37.p13 chr12: 107,231,151-107,231,439 RIC8B
    nsv6472238copy number variation1nstd223human GRCh38 chr12: 106,791,621-106,791,983 , GRCh37.p13 chr12: 107,185,399-107,185,761 RIC8B
    nsv6471812copy number variation1nstd223human GRCh38 chr12: 106,786,960-106,788,866 , GRCh37.p13 chr12: 107,180,738-107,182,644 RIC8B
    nsv6470200copy number variation1nstd223human GRCh38 chr12: 106,857,101-106,857,851 , GRCh37.p13 chr12: 107,250,879-107,251,629 RIC8B
    nsv6466051copy number variation1nstd223human GRCh38 chr12: 106,840,193-106,840,729 , GRCh37.p13 chr12: 107,233,971-107,234,507 RIC8B
    nsv6461841copy number variation1nstd223human GRCh38 chr12: 106,880,106-106,880,121 , GRCh37.p13 chr12: 107,273,884-107,273,899 LOC105369961, RIC8B
    nsv6458352copy number variation1nstd223human GRCh38 chr12: 106,846,445-106,847,018 , GRCh37.p13 chr12: 107,240,223-107,240,796 RIC8B
    nsv6291583copy number variation1nstd102humanPathogenic GRCh37 chr12: 104,230,462-111,984,801 , GRCh38.p12 chr12: 103,836,684-111,546,997 LOC105369964, LOC644746, 147 more genes
    nsv6248564mobile element insertion1nstd215human GRCh38 chr12: 106,871,498-106,871,498 , GRCh37.p13 chr12: 107,265,276-107,265,276 LOC105369961, RIC8B
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