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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3540988insertion1nstd152human GRCh38 (hg38) chr2: 241,471,902-241,471,903 , GRCh37.p13 chr2: 242,411,317-242,411,318 FARP2
    nsv3539868insertion1nstd152human GRCh38 (hg38) chr2: 241,355,972-241,355,973 , GRCh37.p13 chr2: 242,295,387-242,295,388 FARP2
    nsv3536743insertion1nstd152human GRCh38 (hg38) chr2: 241,366,127-241,366,128 , GRCh37.p13 chr2: 242,305,542-242,305,543 FARP2, LOC105373973
    nsv3536035insertion1nstd152human GRCh38 (hg38) chr2: 241,457,684-241,457,685 , GRCh37.p13 chr2: 242,397,099-242,397,100 FARP2
    nsv3531315insertion1nstd152human GRCh38 (hg38) chr2: 241,366,116-241,366,117 , GRCh37.p13 chr2: 242,305,531-242,305,532 FARP2, LOC105373973
    nsv3525352copy number variation2nstd152human GRCh38 (hg38) chr2: 241,471,903-241,472,122 , GRCh37.p13 chr2: 242,411,318-242,411,537 FARP2
    nsv3522050mobile element insertion1nstd152human GRCh38 (hg38) chr2: 241,487,621-241,487,622 , GRCh37.p13 chr2: 242,427,036-242,427,037 FARP2
    nsv3378388copy number variation1nstd162human GRCh38 (hg38) chr2: 241,482,990-241,483,051 , GRCh37.p13 chr2: 242,422,405-242,422,466 FARP2
    nsv3378104insertion4nstd162human GRCh38 (hg38) chr2: 241,457,655-241,457,655 , GRCh37.p13 chr2: 242,397,070-242,397,070 FARP2
    nsv3375432insertion5nstd162human GRCh38 (hg38) chr2: 241,471,903-241,471,903 , GRCh37.p13 chr2: 242,411,318-242,411,318 FARP2
    nsv3373631copy number variation2nstd162human GRCh38 (hg38) chr2: 241,482,929-241,482,990 , GRCh37.p13 chr2: 242,422,344-242,422,405 FARP2
    nsv3371306insertion2nstd162human GRCh38 (hg38) chr2: 241,366,103-241,366,103 , GRCh37.p13 chr2: 242,305,518-242,305,518 FARP2, LOC105373973
    nsv3369641copy number variation1nstd162human GRCh38 (hg38) chr2: 241,457,352-241,457,432 , GRCh37.p13 chr2: 242,396,767-242,396,847 FARP2
    nsv3368450insertion3nstd162human GRCh38 (hg38) chr2: 241,355,969-241,355,969 , GRCh37.p13 chr2: 242,295,384-242,295,384 FARP2
    nsv3367853mobile element insertion2nstd162human GRCh38 (hg38) chr2: 241,487,616-241,487,616 , GRCh37.p13 chr2: 242,427,031-242,427,031 FARP2
    nsv3366739copy number variation1nstd162human GRCh38 (hg38) chr2: 241,355,591-241,355,812 , GRCh37.p13 chr2: 242,295,006-242,295,227 FARP2
    nsv3366620insertion3nstd162human GRCh38 (hg38) chr2: 241,457,796-241,457,796 , GRCh37.p13 chr2: 242,397,211-242,397,211 FARP2
    nsv3363718insertion1nstd162human GRCh38 (hg38) chr2: 241,355,797-241,355,797 , GRCh37.p13 chr2: 242,295,212-242,295,212 FARP2
    nsv3362937insertion1nstd162human GRCh38 (hg38) chr2: 241,457,460-241,457,460 , GRCh37.p13 chr2: 242,396,875-242,396,875 FARP2
    nsv3362671copy number variation1nstd162human GRCh38 (hg38) chr2: 241,417,131-241,422,245 , GRCh37.p13 chr2: 242,356,546-242,361,660 FARP2
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