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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7076847inversion1nstd229human GRCh38 chr12: 120,561,098-121,398,093 , GRCh37.p13 chr12: 120,998,901-121,761,800 MIR4700, P2RX4, 27 more genes
    nsv7068270inversion1nstd229human GRCh38 chr12: 120,747,903-121,406,884 , GRCh37.p13 chr12: 121,185,706-121,761,800 OASL, CLIC1P1, 18 more genes
    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
    nsv6933712copy number variation1nstd229human GRCh38 chr12: 120,870,101-121,037,900 , GRCh37.p13 chr12: 121,307,904-121,475,703 OASL, CLIC1P1, 6 more genes
    nsv6932371copy number variation1nstd229human GRCh38 chr12: 120,970,461-120,976,895 , GRCh37.p13 chr12: 121,408,264-121,414,698 HNF1A, HNF1A-AS1
    nsv6931324copy number variation1nstd229human GRCh38 chr12: 120,893,458-120,984,347 , GRCh37.p13 chr12: 121,331,261-121,422,150 HNF1A-AS1, HNF1A, 4 more genes
    nsv6927984copy number variation1nstd229human GRCh38 chr12: 120,585,344-121,348,343 , GRCh37.p13 chr12: 121,023,147-121,761,800 HNF1A-AS1, LOC105378258, 24 more genes
    nsv6584677inversion1nstd223human GRCh38 chr12: 120,972,624-120,973,808 , GRCh37.p13 chr12: 121,410,427-121,411,611 HNF1A-AS1
    nsv6583876inversion1nstd223human GRCh38 chr12: 118,054,469-123,705,974 , GRCh37.p13 chr12: 118,492,274-124,190,521 RPL11P5, RPL17P37, 159 more genes
    nsv6490079copy number variation1nstd223human GRCh38 chr12: 120,968,126-120,970,917 , GRCh37.p13 chr12: 121,405,929-121,408,720 HNF1A-AS1
    nsv6481678copy number variation1nstd223human GRCh38 chr12: 120,970,604-120,972,096 , GRCh37.p13 chr12: 121,408,407-121,409,899 HNF1A-AS1
    nsv6477060copy number variation1nstd223human GRCh38 chr12: 120,965,548-120,968,243 , GRCh37.p13 chr12: 121,403,351-121,406,046 HNF1A-AS1
    nsv6476788copy number variation1nstd223human GRCh38 chr12: 120,442,140-121,624,181 , GRCh37.p13 chr12: 120,879,943-121,761,800 RNU6-1004P, LOC105370030, 39 more genes
    nsv6290239copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 117,461,902-133,841,395 , GRCh38.p12 chr12: 117,024,097-133,264,809 ACADS, BCL7A, 356 more genes
    nsv6132412copy number variation1nstd213human GRCh37 chr12: 121,000,000-121,550,001 , GRCh38.p12 chr12: 120,562,197-121,112,198 ACADS, HNF1A, 21 more genes
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5555463sequence alteration1nstd206human GRCh38 chr12: 120,561,097-121,398,447 , GRCh37.p13 chr12: 120,998,900-121,761,800 P2RX7, OASL, 27 more genes
    nsv4769360copy number variation1nstd102humanUncertain significance GRCh37 chr12: 121,184,503-121,432,286 , GRCh38.p12 chr12: 120,746,700-120,994,483 HNF1A-AS1, XLOC_009911, 5 more genes
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
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