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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137779copy number variation1nstd102humanBenign GRCh37 chr12: 133,197,450-133,197,510 , GRCh38 chr12: 132,620,864-132,620,924 P2RX2
    nsv5974293insertion1nstd209human GRCh38 chr12: 132,618,235-132,618,235 , GRCh37.p13 chr12: 133,194,821-133,194,821 P2RX2
    nsv5967838insertion1nstd209human GRCh38 chr12: 132,619,201-132,619,201 , GRCh37.p13 chr12: 133,195,787-133,195,787 P2RX2
    nsv5928920copy number variation1nstd209human GRCh38 chr12: 132,620,863-132,620,923 , GRCh37.p13 chr12: 133,197,449-133,197,509 P2RX2
    nsv5585387copy number variation1nstd207human GRCh38 chr12: 132,620,863-132,620,923 , GRCh37.p13 chr12: 133,197,449-133,197,509 P2RX2
    nsv5540371insertion1nstd206human GRCh38 chr12: 132,618,260-132,618,275 , GRCh37.p13 chr12: 133,194,846-133,194,861 P2RX2
    nsv5497692copy number variation1nstd206human GRCh38 chr12: 132,618,668-132,618,766 , GRCh37.p13 chr12: 133,195,254-133,195,352 P2RX2
    nsv5004287copy number variation1nstd200human GRCh38 chr12: 132,594,744-132,628,551 , GRCh37.p13 chr12: 133,171,330-133,205,137 LRCOL1, POLE, 2 more genes
    nsv5004286copy number variation1nstd200human GRCh38 chr12: 132,587,638-132,633,582 , GRCh37.p13 chr12: 133,164,224-133,210,168 LOC105370094, LRCOL1, 2 more genes
    nsv5004285copy number variation1nstd200human GRCh38 chr12: 132,559,993-132,696,891 , GRCh37.p13 chr12: 133,136,579-133,273,477 FBRSL1, LOC105370094, 5 more genes
    nsv4838129copy number variation1nstd200human GRCh37 chr12: 133,136,579-133,273,477 , GRCh38.p12 chr12: 132,559,993-132,696,891 FBRSL1, LRCOL1, 5 more genes
    nsv4741082copy number variation1nstd199human GRCh37 chr12: 133,197,463-133,197,525 , GRCh38.p12 chr12: 132,620,877-132,620,939 P2RX2
    nsv4728857copy number variation1nstd102humanUncertain significance GRCh37 chr12: 133,155,089-133,455,925 , GRCh38.p12 chr12: 132,578,503-132,879,339 PGAM5, RNA5SP379, 13 more genes
    nsv4675409copy number variation1nstd102humanUncertain significance GRCh37 chr12: 133,095,871-133,402,932 , GRCh38.p12 chr12: 132,519,285-132,826,346 MIR6763, RPS11P5, 11 more genes
    nsv4673338copy number variation1nstd186human GRCh37 chr12: 133,196,167-133,196,278 , GRCh38.p12 chr12: 132,619,581-132,619,692 P2RX2
    nsv4672490copy number variation2nstd186human GRCh37 chr12: 133,196,039-133,196,458 , GRCh38.p12 chr12: 132,619,453-132,619,872 P2RX2
    nsv4617976copy number variation2nstd183human GRCh37 chr12: 133,196,167-133,196,278 , GRCh38.p12 chr12: 132,619,581-132,619,692 P2RX2
    nsv4615562copy number variation1nstd183human GRCh37 chr12: 133,196,877-133,197,067 , GRCh38.p12 chr12: 132,620,291-132,620,481 P2RX2
    nsv4605607copy number variation2nstd183human GRCh37 chr12: 133,195,547-133,196,820 , GRCh38.p12 chr12: 132,618,961-132,620,234 P2RX2
    nsv4602307copy number variation2nstd183human GRCh37 chr12: 133,196,039-133,196,458 , GRCh38.p12 chr12: 132,619,453-132,619,872 P2RX2
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