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Items: 1 to 20 of 72

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3116990copy number variation1nstd145human GRCh37 chr5: 158,703,619-158,723,990 , GRCh38.p12 chr5: 159,276,611-159,296,982 UBLCP1
    nsv3084905mobile element insertion1nstd144human GRCh37 chr5: 158,709,434-158,709,434 , GRCh38.p12 chr5: 159,282,426-159,282,426 UBLCP1
    esv3842857copy number variation2estd219human GRCh37 chr5: 158,703,831-158,905,328 , GRCh38.p12 chr5: 159,276,823-159,478,320 , IL12B, 5 more genes
    esv3842858mobile element insertion14estd219human GRCh37 chr5: 158,709,420-158,709,420 , GRCh38.p12 chr5: 159,282,412-159,282,412 UBLCP1
    nsv2742100copy number variation1nstd130human NCBI36 chr5: 158,627,952-158,644,542 , GRCh37.p13 chr5: 158,695,374-158,711,964 , GRCh38.p12 chr5: 159,268,366-159,284,956 UBLCP1
    nsv2728791copy number variation1nstd130human NCBI36 chr5: 158,627,952-158,638,097 , GRCh37.p13 chr5: 158,695,374-158,705,519 , GRCh38.p12 chr5: 159,268,366-159,278,511 UBLCP1
    nsv2386499short tandem repeat1nstd128human GRCh37 chr5: 158,698,465-158,698,485 , GRCh38.p12 chr5: 159,271,457-159,271,477 UBLCP1
    nsv2386498short tandem repeat1nstd128human GRCh37 chr5: 158,697,981-158,697,993 , GRCh38.p12 chr5: 159,270,973-159,270,985 UBLCP1
    nsv2386497short tandem repeat2nstd128human GRCh37 chr5: 158,697,700-158,697,728 , GRCh38.p12 chr5: 159,270,692-159,270,720 UBLCP1
    nsv2385669short tandem repeat2nstd128human GRCh37 chr5: 158,712,402-158,712,422 , GRCh38.p12 chr5: 159,285,394-159,285,414 UBLCP1
    nsv2385668short tandem repeat1nstd128human GRCh37 chr5: 158,707,264-158,707,290 , GRCh38.p12 chr5: 159,280,256-159,280,282 UBLCP1
    nsv2385667short tandem repeat2nstd128human GRCh37 chr5: 158,705,568-158,705,596 , GRCh38.p12 chr5: 159,278,560-159,278,588 UBLCP1
    nsv2385666short tandem repeat3nstd128human GRCh37 chr5: 158,699,419-158,699,432 , GRCh38.p12 chr5: 159,272,411-159,272,424 UBLCP1
    nsv2382930short tandem repeat2nstd128human GRCh37 chr5: 158,706,924-158,706,934 , GRCh38.p12 chr5: 159,279,916-159,279,926 UBLCP1
    nsv2382412short tandem repeat3nstd128human GRCh37 chr5: 158,708,870-158,708,883 , GRCh38.p12 chr5: 159,281,862-159,281,875 UBLCP1
    nsv2382410short tandem repeat10nstd128human GRCh37 chr5: 158,700,843-158,700,877 , GRCh38.p12 chr5: 159,273,835-159,273,869 UBLCP1
    nsv2382409short tandem repeat1nstd128human GRCh37 chr5: 158,698,001-158,698,015 , GRCh38.p12 chr5: 159,270,993-159,271,007 UBLCP1
    nsv2382408short tandem repeat4nstd128human GRCh37 chr5: 158,689,305-158,689,320 , GRCh38.p12 chr5: 159,262,297-159,262,312 UBLCP1
    nsv1177483copy number variation226nstd112Neandertal, Denisova hominin, human GRCh37 chr5: 158,637,042-158,689,959 , GRCh38.p12 chr5: 159,210,034-159,262,951 UBLCP1, RNF145, 2 more genes
    esv3803530tandem duplication1estd192human GRCh37 chr5: 100,573,433-177,051,552 , GRCh38.p12 chr5: 101,237,729-177,624,551 , ARGFXP1, 1156 more genes
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