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Items: 1 to 20 of 423

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075962inversion1nstd229human GRCh38 chr12: 99,728,274-100,301,277 , GRCh37.p13 chr12: 100,122,052-100,695,055 DEPDC4, RN7SL176P, 8 more genes
    nsv7074674inversion1nstd229human GRCh38 chr12: 100,072,817-104,989,567 , GRCh37.p13 chr12: 100,466,595-105,383,345 SYCP3, GOLGA2P5, 84 more genes
    nsv7068612inversion1nstd229human GRCh38 chr12: 100,083,131-104,989,539 , GRCh37.p13 chr12: 100,476,909-105,383,317 EID3, RNU6-1068P, 84 more genes
    nsv6937654copy number variation1nstd229human GRCh38 chr12: 100,023,115-100,025,097 , GRCh37.p13 chr12: 100,416,893-100,418,875 BLTP3B
    nsv6936752copy number variation1nstd229human GRCh38 chr12: 100,009,501-100,143,698 , GRCh37.p13 chr12: 100,403,279-100,537,476 RPS4XP1, BLTP3B
    nsv6935038copy number variation1nstd229human GRCh38 chr12: 100,050,501-100,083,300 , GRCh37.p13 chr12: 100,444,279-100,477,078 BLTP3B
    nsv6934007copy number variation1nstd229human GRCh38 chr12: 100,081,018-100,082,155 , GRCh37.p13 chr12: 100,474,796-100,475,933 BLTP3B
    nsv6932936copy number variation1nstd229human GRCh38 chr12: 100,001,801-100,077,600 , GRCh37.p13 chr12: 100,395,579-100,471,378 BLTP3B, RPS4XP1
    nsv6932882copy number variation1nstd229human GRCh38 chr12: 100,124,100-100,158,017 , GRCh37.p13 chr12: 100,517,878-100,551,795 GOLGA2P5, DNM1P19, 2 more genes
    nsv6932257copy number variation1nstd229human GRCh38 chr12: 99,991,565-100,062,831 , GRCh37.p13 chr12: 100,385,343-100,456,609 BLTP3B, RPS4XP1
    nsv6932064copy number variation1nstd229human GRCh38 chr12: 100,091,176-100,186,453 , GRCh37.p13 chr12: 100,484,954-100,580,231 RN7SL176P, BLTP3B, 2 more genes
    nsv6931991copy number variation1nstd229human GRCh38 chr12: 99,880,978-100,084,733 , GRCh37.p13 chr12: 100,274,756-100,478,511 ANKS1B, RPS4XP1, 1 more genes
    nsv6931456copy number variation1nstd229human GRCh38 chr12: 100,025,901-100,043,300 , GRCh37.p13 chr12: 100,419,679-100,437,078 BLTP3B
    nsv6930119copy number variation1nstd229human GRCh38 chr12: 100,017,042-100,033,255 , GRCh37.p13 chr12: 100,410,820-100,427,033 BLTP3B
    nsv6929036copy number variation1nstd229human GRCh38 chr12: 100,060,121-100,062,889 , GRCh37.p13 chr12: 100,453,899-100,456,667 BLTP3B
    nsv6927390copy number variation1nstd229human GRCh38 chr12: 100,080,780-100,080,843 , GRCh37.p13 chr12: 100,474,558-100,474,621 BLTP3B
    nsv6926514copy number variation1nstd229human GRCh38 chr12: 99,947,178-100,328,732 , GRCh37.p13 chr12: 100,340,956-100,722,510 BLTP3B, MIR1827, 8 more genes
    nsv6924539copy number variation1nstd229human GRCh38 chr12: 100,130,649-100,133,159 , GRCh37.p13 chr12: 100,524,427-100,526,937 BLTP3B
    nsv6924399copy number variation1nstd229human GRCh38 chr12: 100,130,458-100,134,216 , GRCh37.p13 chr12: 100,524,236-100,527,994 BLTP3B
    nsv6924185copy number variation1nstd229human GRCh38 chr12: 99,875,995-100,051,152 , GRCh37.p13 chr12: 100,269,773-100,444,930 ANKS1B, RPS4XP1, 1 more genes
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