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Items: 1 to 20 of 742

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142207insertion1nstd232human GRCh37.p13 chr9: 128,305,444-128,305,444 , GRCh38.p12 chr9: 125,543,165-125,543,165 MAPKAP1
    nsv7139198insertion1nstd232human GRCh37.p13 chr9: 128,305,447-128,305,447 , GRCh38.p12 chr9: 125,543,168-125,543,168 MAPKAP1
    nsv7137806insertion1nstd232human GRCh37.p13 chr9: 128,420,081-128,420,081 , GRCh38.p12 chr9: 125,657,802-125,657,802 MAPKAP1
    nsv7072147inversion1nstd229human GRCh38 chr9: 125,655,339-125,663,592 , GRCh37.p13 chr9: 128,417,618-128,425,871 MAPKAP1
    nsv7071535inversion1nstd229human GRCh38 chr9: 124,246,999-128,875,010 , GRCh37.p13 chr9: 127,009,278-131,637,289 PTGES2-AS1, STXBP1, 130 more genes
    nsv6877396copy number variation1nstd229human GRCh38 chr9: 125,470,347-125,471,084 , GRCh37.p13 chr9: 128,232,626-128,233,363 MAPKAP1
    nsv6877172copy number variation1nstd229human GRCh38 chr9: 125,450,832-125,450,860 , GRCh37.p13 chr9: 128,213,111-128,213,139 MAPKAP1
    nsv6876160copy number variation1nstd229human GRCh38 chr9: 125,445,848-125,447,657 , GRCh37.p13 chr9: 128,208,127-128,209,936 MAPKAP1
    nsv6875281copy number variation1nstd229human GRCh38 chr9: 125,678,954-125,683,125 , GRCh37.p13 chr9: 128,441,233-128,445,404 MAPKAP1
    nsv6875192copy number variation1nstd229human GRCh38 chr9: 125,491,503-125,495,959 , GRCh37.p13 chr9: 128,253,782-128,258,238 MAPKAP1
    nsv6874333copy number variation1nstd229human GRCh38 chr9: 125,531,601-125,537,843 , GRCh37.p13 chr9: 128,293,880-128,300,122 MAPKAP1
    nsv6874288copy number variation1nstd229human GRCh38 chr9: 125,641,768-125,650,522 , GRCh37.p13 chr9: 128,404,047-128,412,801 MAPKAP1
    nsv6874192copy number variation1nstd229human GRCh38 chr9: 125,560,022-125,563,490 , GRCh37.p13 chr9: 128,322,301-128,325,769 MAPKAP1
    nsv6874176copy number variation1nstd229human GRCh38 chr9: 125,525,730-125,525,888 , GRCh37.p13 chr9: 128,288,009-128,288,167 MAPKAP1
    nsv6872734copy number variation1nstd229human GRCh38 chr9: 125,604,939-125,607,476 , GRCh37.p13 chr9: 128,367,218-128,369,755 MAPKAP1
    nsv6872082copy number variation1nstd229human GRCh38 chr9: 125,612,745-125,614,682 , GRCh37.p13 chr9: 128,375,024-128,376,961 MAPKAP1
    nsv6871554copy number variation1nstd229human GRCh38 chr9: 125,481,288-125,481,351 , GRCh37.p13 chr9: 128,243,567-128,243,630 MAPKAP1
    nsv6870475copy number variation1nstd229human GRCh38 chr9: 125,646,071-125,646,145 , GRCh37.p13 chr9: 128,408,350-128,408,424 MAPKAP1
    nsv6870259copy number variation1nstd229human GRCh38 chr9: 125,640,786-125,647,150 , GRCh37.p13 chr9: 128,403,065-128,409,429 MAPKAP1
    nsv6869427copy number variation1nstd229human GRCh38 chr9: 125,510,335-125,511,968 , GRCh37.p13 chr9: 128,272,614-128,274,247 RN7SL30P, MAPKAP1
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