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Items: 1 to 20 of 332

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129768insertion1nstd186human GRCh37 chr12: 121,568,663-121,568,673 , GRCh38.p12 chr12: 121,130,860-121,130,870 P2RX7, LOC105370032
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5972771insertion1nstd209human GRCh38 chr12: 121,136,023-121,136,023 , GRCh37.p13 chr12: 121,573,826-121,573,826 P2RX7, LOC105370032
    nsv5968623insertion1nstd209human GRCh38 chr12: 121,130,819-121,130,819 , GRCh37.p13 chr12: 121,568,622-121,568,622 P2RX7, LOC105370032
    nsv5936988copy number variation1nstd209human GRCh38 chr12: 121,185,781-121,204,039 , GRCh37.p13 chr12: 121,623,584-121,641,842 P2RX7, LOC105370032
    nsv5855631copy number variation1nstd209human GRCh38 chr12: 121,143,687-121,146,355 , GRCh37.p13 chr12: 121,581,490-121,584,158 LOC105370032, P2RX7
    nsv5854281copy number variation1nstd209human GRCh38 chr12: 121,145,686-121,151,755 , GRCh37.p13 chr12: 121,583,489-121,589,558 LOC105370032, P2RX7
    nsv5852235copy number variation1nstd209human GRCh38 chr12: 121,143,686-121,148,605 , GRCh37.p13 chr12: 121,581,489-121,586,408 P2RX7, LOC105370032
    nsv5848153copy number variation1nstd209human GRCh38 chr12: 121,185,714-121,192,880 , GRCh37.p13 chr12: 121,623,517-121,630,683 P2RX7, LOC105370032
    nsv5711787mobile element insertion1nstd211human GRCh38 chr12: 121,155,241-121,155,241 , GRCh37.p13 chr12: 121,593,044-121,593,044 P2RX7, LOC105370032
    nsv5646481insertion1nstd207human GRCh38 chr12: 121,130,843-121,130,843 , GRCh37.p13 chr12: 121,568,646-121,568,646 P2RX7, LOC105370032
    nsv5555463sequence alteration1nstd206human GRCh38 chr12: 120,561,097-121,398,447 , GRCh37.p13 chr12: 120,998,900-121,761,800 P2RX7, OASL, 27 more genes
    nsv5543677insertion1nstd206human GRCh38 chr12: 121,130,860-121,130,870 , GRCh37.p13 chr12: 121,568,663-121,568,673 P2RX7, LOC105370032
    nsv5509282copy number variation1nstd206human GRCh38 chr12: 121,185,785-121,204,040 , GRCh37.p13 chr12: 121,623,588-121,641,843 LOC105370032, P2RX7
    nsv5507259copy number variation1nstd206human GRCh38 chr12: 121,067,073-121,153,684 , GRCh37.p13 chr12: 121,504,876-121,591,487 P2RX7, LOC105370030, 3 more genes
    nsv5502555copy number variation1nstd206human GRCh38 chr12: 121,161,634-121,164,561 , GRCh37.p13 chr12: 121,599,437-121,602,364 P2RX7, LOC105370032
    nsv5502009copy number variation1nstd206human GRCh38 chr12: 121,131,357-121,132,135 , GRCh37.p13 chr12: 121,569,160-121,569,938 LOC105370032, P2RX7
    nsv5500437copy number variation1nstd206human GRCh38 chr12: 121,176,504-121,179,318 , GRCh37.p13 chr12: 121,614,307-121,617,121 P2RX7, LOC105370032
    nsv5498174copy number variation1nstd206human GRCh38 chr12: 121,134,059-121,135,074 , GRCh37.p13 chr12: 121,571,862-121,572,877 P2RX7, LOC105370032
    nsv5497325copy number variation1nstd206human GRCh38 chr12: 121,164,341-121,167,482 , GRCh37.p13 chr12: 121,602,144-121,605,285 P2RX7, LOC105370032
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