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Items: 1 to 20 of 544

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148098copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 121,890,923-122,473,333 , GRCh38.p12 chr12: 121,453,120-122,035,427 BCL7A, HPD, 14 more genes
    nsv7148095copy number variation1nstd102humanUncertain significance GRCh37 chr12: 121,341,598-124,103,434 , GRCh38.p12 chr12: 120,903,795-123,618,887 ANAPC5, MLXIP, 82 more genes
    nsv7075554inversion1nstd229human GRCh38 chr12: 121,447,939-121,448,208 , GRCh37.p13 chr12: 121,885,742-121,886,011 , GRCh37.p13 chr12|NW_004504303.2: 123,942-124,211 KDM2B
    nsv7068270inversion1nstd229human GRCh38 chr12: 120,747,903-121,406,884 , GRCh37.p13 chr12: 121,185,706-121,761,800 OASL, CLIC1P1, 18 more genes
    nsv7062780inversion1nstd229human GRCh38 chr12: 121,074,381-121,634,791 , GRCh37.p13 chr12|NW_004504303.2: 1-310,795 , GRCh37.p13 chr12: 121,761,801-122,072,697 P2RX7, ANAPC5, 12 more genes
    nsv6937790copy number variation1nstd229human GRCh38 chr12: 121,527,667-121,530,169 , GRCh37.p13 chr12|NW_004504303.2: 203,670-206,172 , GRCh37.p13 chr12: 121,965,572-121,968,074 KDM2B
    nsv6934866copy number variation1nstd229human GRCh38 chr12: 119,918,701-123,974,100 , GRCh37.p13 chr12: 120,356,505-124,458,647 RNU6-1088P, LOC105370042, 130 more genes
    nsv6934735copy number variation1nstd229human GRCh38 chr12: 121,458,834-121,462,850 , GRCh37.p13 chr12|NW_004504303.2: 134,837-138,853 , GRCh37.p13 chr12: 121,896,637-121,900,653 KDM2B
    nsv6934313copy number variation1nstd229human GRCh38 chr12: 121,479,912-121,482,591 , GRCh37.p13 chr12|NW_004504303.2: 155,915-158,594 , GRCh37.p13 chr12: 121,917,715-121,920,394 KDM2B
    nsv6933327copy number variation1nstd229human GRCh38 chr12: 121,538,901-121,542,800 , GRCh37.p13 chr12: 121,976,806-121,980,705 , GRCh37.p13 chr12|NW_004504303.2: 214,904-218,803 KDM2B
    nsv6932368copy number variation1nstd229human GRCh38 chr12: 121,416,801-121,427,300 , GRCh37.p13 chr12|NW_004504303.2: 92,804-103,303 , GRCh37.p13 chr12: 121,854,604-121,865,103 RNF34, KDM2B
    nsv6930248copy number variation1nstd229human GRCh38 chr12: 121,469,743-121,481,001 , GRCh37.p13 chr12|NW_004504303.2: 145,746-157,004 , GRCh37.p13 chr12: 121,907,546-121,918,804 KDM2B
    nsv6928029copy number variation1nstd229human GRCh38 chr12: 121,478,803-121,490,802 , GRCh37.p13 chr12|NW_004504303.2: 154,806-166,805 , GRCh37.p13 chr12: 121,916,606-121,928,605 KDM2B
    nsv6927420copy number variation1nstd229human GRCh38 chr12: 121,431,428-121,431,585 , GRCh37.p13 chr12: 121,869,231-121,869,388 , GRCh37.p13 chr12|NW_004504303.2: 107,431-107,588 KDM2B
    nsv6927245copy number variation1nstd229human GRCh38 chr12: 121,402,441-121,405,189 , GRCh37.p13 chr12|NW_004504303.2: 78,444-81,192 , GRCh37.p13 chr12: 121,840,244-121,842,992 KDM2B, RNF34
    nsv6927231copy number variation1nstd229human GRCh38 chr12: 121,554,703-121,557,444 , GRCh37.p13 chr12: 121,992,608-121,995,349 , GRCh37.p13 chr12|NW_004504303.2: 230,706-233,447 KDM2B
    nsv6926511copy number variation1nstd229human GRCh38 chr12: 121,539,752-121,542,341 , GRCh37.p13 chr12: 121,977,657-121,980,246 , GRCh37.p13 chr12|NW_004504303.2: 215,755-218,344 KDM2B
    nsv6925897copy number variation1nstd229human GRCh38 chr12: 121,411,117-121,414,854 , GRCh37.p13 chr12|NW_004504303.2: 87,120-90,857 , GRCh37.p13 chr12: 121,848,920-121,852,657 KDM2B, RNF34
    nsv6925171copy number variation1nstd229human GRCh38 chr12: 121,517,078-121,519,311 , GRCh37.p13 chr12: 121,954,881-121,957,114 , GRCh37.p13 chr12|NW_004504303.2: 193,081-195,314 KDM2B
    nsv6924722copy number variation1nstd229human GRCh38 chr12: 121,557,821-121,790,173 , GRCh37.p13 chr12: 122,096,825-122,228,079 KDM2B-DT, RNU6-1004P, 6 more genes
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