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Items: 1 to 20 of 264

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077519inversion1nstd229human GRCh38 chr12: 86,495,718-92,133,299 , GRCh37.p13 chr12: 86,889,495-92,527,075 CEP290, MIR3059, 60 more genes
    nsv7060010inversion1nstd229human GRCh38 chr12: 86,085,575-91,207,469 , GRCh37.p13 chr12: 86,479,353-91,601,246 POC1B, C12orf50, 55 more genes
    nsv6937405copy number variation1nstd229human GRCh38 chr12: 87,957,217-88,286,316 , GRCh37.p13 chr12: 88,350,994-88,680,093 RNA5SP364, LOC107984542, 6 more genes
    nsv6934258copy number variation1nstd229human GRCh38 chr12: 88,162,601-88,164,700 , GRCh37.p13 chr12: 88,556,378-88,558,477 TMTC3
    nsv6932987copy number variation1nstd229human GRCh38 chr12: 87,925,501-88,494,507 , GRCh37.p13 chr12: 88,319,278-88,888,284 LOC107984542, RPS4XP15, 8 more genes
    nsv6929928copy number variation1nstd229human GRCh38 chr12: 87,978,901-88,153,800 , GRCh37.p13 chr12: 88,372,678-88,547,577 CEP290, C12orf50, 5 more genes
    nsv6927462copy number variation1nstd229human GRCh38 chr12: 88,175,961-88,214,906 , GRCh37.p13 chr12: 88,569,738-88,608,683 TMTC3
    nsv6925267copy number variation1nstd229human GRCh38 chr12: 88,047,969-88,320,569 , GRCh37.p13 chr12: 88,441,746-88,714,346 RLIG1, RNA5SP364, 4 more genes
    nsv6622093copy number variation2nstd224human GRCh37 chr12: 88,519,120-88,553,930 , GRCh38.p12 chr12: 88,125,343-88,160,153 CEP290, TMTC3
    nsv6622092copy number variation2nstd224human GRCh37 chr12: 88,500,847-88,553,930 , GRCh38.p12 chr12: 88,107,070-88,160,153 CEP290, TMTC3
    nsv6622090copy number variation2nstd224human GRCh37 chr12: 88,454,677-88,553,930 , GRCh38.p12 chr12: 88,060,900-88,160,153 TMTC3, CEP290
    nsv6621896copy number variation2nstd224human GRCh37 chr12: 88,502,847-88,553,930 , GRCh38.p12 chr12: 88,109,070-88,160,153 TMTC3, CEP290
    nsv6581988inversion1nstd223human GRCh38 chr12: 88,163,205-88,164,175 , GRCh37.p13 chr12: 88,556,982-88,557,952 TMTC3
    nsv6576036inversion1nstd223human GRCh38 chr12: 88,162,945-88,164,134 , GRCh37.p13 chr12: 88,556,722-88,557,911 TMTC3
    nsv6474732copy number variation1nstd223human GRCh38 chr12: 88,174,001-88,175,200 , GRCh37.p13 chr12: 88,567,778-88,568,977 TMTC3
    nsv6472928copy number variation1nstd223human GRCh38 chr12: 88,159,701-88,162,800 , GRCh37.p13 chr12: 88,553,478-88,556,577 TMTC3
    nsv6467933copy number variation1nstd223human GRCh38 chr12: 88,148,774-88,149,126 , GRCh37.p13 chr12: 88,542,551-88,542,903 TMTC3
    nsv6465284copy number variation1nstd223human GRCh38 chr12: 88,193,644-88,194,161 , GRCh37.p13 chr12: 88,587,421-88,587,938 TMTC3
    nsv6463506copy number variation1nstd223human GRCh38 chr12: 88,194,893-88,195,338 , GRCh37.p13 chr12: 88,588,670-88,589,115 TMTC3
    nsv6463207copy number variation1nstd223human GRCh38 chr12: 88,153,501-88,154,700 , GRCh37.p13 chr12: 88,547,278-88,548,477 TMTC3
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