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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7070411inversion1nstd229human GRCh38 chr12: 18,693,159-18,696,634 , GRCh37.p13 chr12: 18,846,093-18,849,568 PSMC1P9, PIK3C2G, 1 more genes
    nsv6933770copy number variation1nstd229human GRCh38 chr12: 18,690,001-18,694,800 , GRCh37.p13 chr12: 18,842,935-18,847,734 PIK3C2G, PLCZ1, 1 more genes
    nsv6931605copy number variation1nstd229human GRCh38 chr12: 18,709,935-18,711,935 , GRCh37.p13 chr12: 18,862,869-18,864,869 PIK3C2G, PLCZ1
    nsv6930705copy number variation1nstd229human GRCh38 chr12: 18,705,342-18,726,169 , GRCh37.p13 chr12: 18,858,276-18,879,103 PIK3C2G, PLCZ1
    nsv6928235copy number variation1nstd229human GRCh38 chr12: 18,659,692-18,659,717 , GRCh37.p13 chr12: 18,812,626-18,812,651 PLCZ1, PIK3C2G
    nsv6927823copy number variation1nstd229human GRCh38 chr12: 18,733,701-18,739,000 , GRCh37.p13 chr12: 18,886,635-18,891,934 CAPZA3, PLCZ1
    nsv6927743copy number variation1nstd229human GRCh38 chr12: 18,719,604-18,720,037 , GRCh37.p13 chr12: 18,872,538-18,872,971 PLCZ1
    nsv6927089copy number variation1nstd229human GRCh38 chr12: 18,689,501-18,691,700 , GRCh37.p13 chr12: 18,842,435-18,844,634 PIK3C2G, PLCZ1, 1 more genes
    nsv6926487copy number variation1nstd229human GRCh38 chr12: 18,660,108-18,670,892 , GRCh37.p13 chr12: 18,813,042-18,823,826 PLCZ1, PIK3C2G
    nsv6925550copy number variation1nstd229human GRCh38 chr12: 18,686,475-18,686,527 , GRCh37.p13 chr12: 18,839,409-18,839,461 PIK3C2G, PLCZ1
    nsv6923694copy number variation1nstd229human GRCh38 chr12: 18,729,960-18,762,398 , GRCh37.p13 chr12: 18,882,894-18,915,332 CAPZA3, PLCZ1, 1 more genes
    nsv6920371copy number variation1nstd229human GRCh38 chr12: 18,731,201-18,742,100 , GRCh37.p13 chr12: 18,884,135-18,895,034 PLCZ1, CAPZA3
    nsv6919907copy number variation1nstd229human GRCh38 chr12: 18,737,901-18,741,100 , GRCh37.p13 chr12: 18,890,835-18,894,034 PLCZ1, CAPZA3
    nsv6919540copy number variation1nstd229human GRCh38 chr12: 18,651,634-18,656,817 , GRCh37.p13 chr12: 18,804,568-18,809,751 PLCZ1, PIK3C2G
    nsv6919338copy number variation1nstd229human GRCh38 chr12: 18,357,672-19,155,144 , GRCh37.p13 chr12: 18,510,606-19,308,078 RPL7P6, LOC102724227, 9 more genes
    nsv6637268copy number variation1nstd102humanUncertain significance GRCh37 chr12: 18,636,979-18,799,315 , GRCh38.p12 chr12: 18,484,045-18,646,381 PIK3C2G, ZKSCAN7P1, 1 more genes
    nsv6634456copy number variation1nstd102humanPathogenic GRCh37 chr12: 10,853,887-24,103,810 , GRCh38.p12 chr12: 10,701,288-23,950,876 TAS2R15P, LOC105369673, 209 more genes
    nsv6588563inversion1nstd223human GRCh38 chr12: 18,704,482-18,705,829 , GRCh37.p13 chr12: 18,857,416-18,858,763 PIK3C2G, PLCZ1
    nsv6473837copy number variation1nstd223human GRCh38 chr12: 18,674,901-18,675,520 , GRCh37.p13 chr12: 18,827,835-18,828,454 PLCZ1, PIK3C2G
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