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Items: 1 to 20 of 71

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2073383copy number variation1estd194human NCBI36 chr5: 10,308,450-10,308,452 , GRCh37.p13 chr5: 10,255,450-10,255,452 , GRCh38.p12 chr5: 10,255,338-10,255,340 CCT5
    esv2063303copy number variation1estd194human NCBI36 chr5: 10,316,464-10,316,466 , GRCh37.p13 chr5: 10,263,464-10,263,466 , GRCh38.p12 chr5: 10,263,352-10,263,354 CCT5
    esv2115938insertion1estd194human NCBI36 chr5: 10,306,441-10,306,441 , GRCh37.p13 chr5: 10,253,441-10,253,441 , GRCh38.p12 chr5: 10,253,329-10,253,329 CCT5
    esv1981628copy number variation1estd194human NCBI36 chr5: 10,301,340-10,301,345 , GRCh37.p13 chr5: 10,248,340-10,248,345 , GRCh38.p12 chr5: 10,248,228-10,248,233 CCT5, ATPSCKMT
    esv1956063copy number variation1estd194human NCBI36 chr5: 10,319,881-10,319,885 , GRCh37.p13 chr5: 10,266,881-10,266,885 , GRCh38.p12 chr5: 10,266,769-10,266,773 CCT5
    esv1939049insertion1estd194human NCBI36 chr5: 10,318,887-10,318,887 , GRCh37.p13 chr5: 10,265,887-10,265,887 , GRCh38.p12 chr5: 10,265,775-10,265,775 CCT5
    esv2003701copy number variation1estd194human NCBI36 chr5: 10,319,362-10,319,363 , GRCh37.p13 chr5: 10,266,362-10,266,363 , GRCh38.p12 chr5: 10,266,250-10,266,251 CCT5
    esv2039203copy number variation1estd194human NCBI36 chr5: 10,305,579-10,305,583 , GRCh37.p13 chr5: 10,252,579-10,252,583 , GRCh38.p12 chr5: 10,252,467-10,252,471 CCT5
    esv2018684copy number variation1estd194human NCBI36 chr5: 10,319,957-10,319,961 , GRCh37.p13 chr5: 10,266,957-10,266,961 , GRCh38.p12 chr5: 10,266,845-10,266,849 CCT5
    esv2553121copy number variation1estd197human NCBI36 chr5: 10,319,957-10,319,960 , GRCh37.p13 chr5: 10,266,957-10,266,960 , GRCh38.p12 chr5: 10,266,845-10,266,848 CCT5
    esv2629765copy number variation1estd197human NCBI36 chr5: 10,319,881-10,319,884 , GRCh37.p13 chr5: 10,266,881-10,266,884 , GRCh38.p12 chr5: 10,266,769-10,266,772 CCT5
    esv2543879copy number variation1estd197human NCBI36 chr5: 10,319,366-10,319,366 , GRCh37.p13 chr5: 10,266,366-10,266,366 , GRCh38.p12 chr5: 10,266,254-10,266,254 CCT5
    esv2505304copy number variation1estd197human NCBI36 chr5: 10,319,362-10,319,362 , GRCh37.p13 chr5: 10,266,362-10,266,362 , GRCh38.p12 chr5: 10,266,250-10,266,250 CCT5
    esv2555032insertion1estd197human NCBI36 chr5: 10,317,388-10,317,388 , GRCh37.p13 chr5: 10,264,388-10,264,388 , GRCh38.p12 chr5: 10,264,276-10,264,276 CCT5
    esv2430846insertion1estd197human NCBI36 chr5: 10,313,656-10,313,656 , GRCh37.p13 chr5: 10,260,656-10,260,656 , GRCh38.p12 chr5: 10,260,544-10,260,544 CCT5
    esv2429146insertion1estd197human NCBI36 chr5: 10,308,096-10,308,096 , GRCh37.p13 chr5: 10,255,096-10,255,096 , GRCh38.p12 chr5: 10,254,984-10,254,984 CCT5
    esv2534305copy number variation1estd197human NCBI36 chr5: 10,301,340-10,301,344 , GRCh37.p13 chr5: 10,248,340-10,248,344 , GRCh38.p12 chr5: 10,248,228-10,248,232 ATPSCKMT, CCT5
    esv1820413copy number variation1estd188human NCBI36 chr5: 10,316,692-10,327,711 , GRCh37.p13 chr5: 10,263,692-10,274,711 , GRCh38.p12 chr5: 10,263,580-10,274,599 CCT5
    esv1828247copy number variation1estd188human NCBI36 chr5: 10,319,067-10,327,615 , GRCh37.p13 chr5: 10,266,067-10,274,615 , GRCh38.p12 chr5: 10,265,955-10,274,503 CCT5
    esv1846552copy number variation1estd188human NCBI36 chr5: 10,316,692-10,327,711 , GRCh37.p13 chr5: 10,263,692-10,274,711 , GRCh38.p12 chr5: 10,263,580-10,274,599 CCT5
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