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Items: 1 to 20 of 535

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148221copy number variation1nstd102humanPathogenic GRCh38 chr6: 150,905,553-158,511,926 , GRCh37.p13 chr6: 151,226,689-158,932,958 RNU6-824P, LOC105378067, 97 more genes
    nsv7140463insertion1nstd232human GRCh37.p13 chr6: 151,574,550-151,574,550 , GRCh38.p12 chr6: 151,253,415-151,253,415 AKAP12
    nsv7042877inversion1nstd229human GRCh38 chr6: 149,723,719-152,206,487 , GRCh37.p13 chr6: 150,044,855-152,527,622 MTHFD1L, RAET1F, 48 more genes
    nsv7041422inversion1nstd229human GRCh38 chr6: 150,201,394-154,373,035 , GRCh37.p13 chr6: 150,522,530-154,694,169 MTHFD1L, MYCT1, 56 more genes
    nsv6816899copy number variation1nstd229human GRCh38 chr6: 150,907,083-151,349,847 , GRCh37.p13 chr6: 151,228,219-151,670,982 MTHFD1L, RNU6-302P, 10 more genes
    nsv6816139copy number variation1nstd229human GRCh38 chr6: 151,077,301-151,497,900 , GRCh37.p13 chr6: 151,398,437-151,819,035 LOC102723831, ARMT1, 13 more genes
    nsv6815749copy number variation1nstd229human GRCh38 chr6: 151,307,945-151,343,051 , GRCh37.p13 chr6: 151,629,080-151,664,186 AKAP12, RN7SKP268
    nsv6815520copy number variation1nstd229human GRCh38 chr6: 151,340,226-151,345,370 , GRCh37.p13 chr6: 151,661,361-151,666,505 AKAP12
    nsv6815123copy number variation1nstd229human GRCh38 chr6: 151,331,650-151,334,035 , GRCh37.p13 chr6: 151,652,785-151,655,170 AKAP12
    nsv6814399copy number variation1nstd229human GRCh38 chr6: 151,250,725-151,278,708 , GRCh37.p13 chr6: 151,571,860-151,599,843 RNU6-1247P, AKAP12
    nsv6807402copy number variation1nstd229human GRCh38 chr6: 151,075,901-151,743,600 , GRCh37.p13 chr6: 151,397,037-152,064,735 RNU6-813P, ARMT1, 16 more genes
    nsv6806891copy number variation1nstd229human GRCh38 chr6: 151,339,662-151,346,170 , GRCh37.p13 chr6: 151,660,797-151,667,305 AKAP12
    nsv6806661copy number variation1nstd229human GRCh38 chr6: 151,333,701-151,336,300 , GRCh37.p13 chr6: 151,654,836-151,657,435 AKAP12
    nsv6806430copy number variation1nstd229human GRCh38 chr6: 150,408,652-151,352,315 , GRCh37.p13 chr6: 150,729,788-151,673,450 RNU6-1247P, RPS12P11, 13 more genes
    nsv6804980copy number variation1nstd229human GRCh38 chr6: 151,322,683-151,322,741 , GRCh37.p13 chr6: 151,643,818-151,643,876 AKAP12
    nsv6804611copy number variation1nstd229human GRCh38 chr6: 151,319,530-151,319,567 , GRCh37.p13 chr6: 151,640,665-151,640,702 RN7SKP268, AKAP12
    nsv6803081copy number variation1nstd229human GRCh38 chr6: 151,268,656-151,277,243 , GRCh37.p13 chr6: 151,589,791-151,598,378 AKAP12
    nsv6802260copy number variation1nstd229human GRCh38 chr6: 151,297,017-151,302,642 , GRCh37.p13 chr6: 151,618,152-151,623,777 AKAP12, RNY4P20
    nsv6800813copy number variation1nstd229human GRCh38 chr6: 151,346,509-151,350,605 , GRCh37.p13 chr6: 151,667,644-151,671,740 AKAP12
    nsv6799574copy number variation1nstd229human GRCh38 chr6: 151,335,297-151,371,468 , GRCh37.p13 chr6: 151,656,432-151,692,603 ZBTB2, AKAP12
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