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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077035inversion1nstd229human GRCh38 chr12: 47,095,002-47,101,876 , GRCh37.p13 chr12: 47,488,785-47,495,659 PCED1B
    nsv7074786inversion1nstd229human GRCh38 chr12: 47,059,202-48,408,098 , GRCh37.p13 chr12: 47,452,985-48,801,881 LOC102725258, RPAP3, 42 more genes
    nsv7065013inversion1nstd229human GRCh38 chr12: 47,096,706-47,101,122 , GRCh37.p13 chr12: 47,490,489-47,494,905 PCED1B
    nsv7064732inversion1nstd229human GRCh38 chr12: 47,092,039-47,096,684 , GRCh37.p13 chr12: 47,485,822-47,490,467 PCED1B
    nsv6937972copy number variation1nstd229human GRCh38 chr12: 47,209,937-47,351,090 , GRCh37.p13 chr12: 47,603,720-47,744,873 PCED1B-AS1, PPIAP45, 3 more genes
    nsv6937658copy number variation1nstd229human GRCh38 chr12: 47,212,301-47,218,100 , GRCh37.p13 chr12: 47,606,084-47,611,883 PCED1B, PCED1B-AS1
    nsv6937553copy number variation1nstd229human GRCh38 chr12: 47,139,123-47,143,440 , GRCh37.p13 chr12: 47,532,906-47,537,223 PCED1B
    nsv6936779copy number variation1nstd229human GRCh38 chr12: 47,150,244-47,156,180 , GRCh37.p13 chr12: 47,544,027-47,549,963 PCED1B
    nsv6936552copy number variation1nstd229human GRCh38 chr12: 47,191,880-47,221,483 , GRCh37.p13 chr12: 47,585,663-47,615,266 PCED1B-AS1, PCED1B
    nsv6935808copy number variation1nstd229human GRCh38 chr12: 47,225,448-47,228,318 , GRCh37.p13 chr12: 47,619,231-47,622,101 PCED1B
    nsv6934986copy number variation1nstd229human GRCh38 chr12: 47,078,733-47,079,172 , GRCh37.p13 chr12: 47,472,516-47,472,955 PCED1B, AMIGO2
    nsv6934928copy number variation1nstd229human GRCh38 chr12: 46,972,513-47,289,021 , GRCh37.p13 chr12: 47,366,296-47,682,804 IFITM3P6, AMIGO2, 5 more genes
    nsv6934833copy number variation1nstd229human GRCh38 chr12: 47,215,797-47,215,876 , GRCh37.p13 chr12: 47,609,580-47,609,659 PCED1B-AS1, PCED1B
    nsv6933250copy number variation1nstd229human GRCh38 chr12: 47,116,730-47,143,385 , GRCh37.p13 chr12: 47,510,513-47,537,168 PCED1B, IFITM3P6
    nsv6933227copy number variation1nstd229human GRCh38 chr12: 47,201,661-47,201,813 , GRCh37.p13 chr12: 47,595,444-47,595,596 PCED1B
    nsv6931454copy number variation1nstd229human GRCh38 chr12: 47,110,501-47,119,400 , GRCh37.p13 chr12: 47,504,284-47,513,183 PCED1B
    nsv6930293copy number variation1nstd229human GRCh38 chr12: 47,072,885-47,079,716 , GRCh37.p13 chr12: 47,466,668-47,473,499 PCED1B, AMIGO2
    nsv6929514copy number variation1nstd229human GRCh38 chr12: 47,203,860-47,206,392 , GRCh37.p13 chr12: 47,597,643-47,600,175 PCED1B
    nsv6929115copy number variation1nstd229human GRCh38 chr12: 47,119,854-47,124,090 , GRCh37.p13 chr12: 47,513,637-47,517,873 PCED1B
    nsv6926146copy number variation1nstd229human GRCh38 chr12: 47,233,127-47,234,209 , GRCh37.p13 chr12: 47,626,910-47,627,992 PCED1B
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