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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076847inversion1nstd229human GRCh38 chr12: 120,561,098-121,398,093 , GRCh37.p13 chr12: 120,998,901-121,761,800 MIR4700, P2RX4, 27 more genes
    nsv6937005copy number variation1nstd229human GRCh38 chr12: 120,465,601-120,774,200 , GRCh37.p13 chr12: 120,903,404-121,212,003 DYNLL1, RNF10, 14 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
    nsv6934829copy number variation1nstd229human GRCh38 chr12: 120,648,482-120,812,433 , GRCh37.p13 chr12: 121,086,285-121,250,236 ACADS, LOC105370029, 5 more genes
    nsv6934467copy number variation1nstd229human GRCh38 chr12: 120,407,101-120,775,400 , GRCh37.p13 chr12: 120,844,904-121,213,203 SPPL3, RPL31P52, 18 more genes
    nsv6933965copy number variation1nstd229human GRCh38 chr12: 120,703,901-120,751,800 , GRCh37.p13 chr12: 121,141,704-121,189,603 MIR4700, ACADS, 1 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
    nsv6919599copy number variation1nstd229human GRCh38 chr12: 119,989,801-120,740,500 , GRCh37.p13 chr12: 120,427,605-121,178,303 RPS20P31, MLEC, 33 more genes
    nsv6637490copy number variation1nstd102humanUncertain significance GRCh37 chr12: 120,761,046-121,280,839 , GRCh38.p12 chr12: 120,323,243-120,843,036 RPS27P25, MIR4700, 22 more genes
    nsv6583876inversion1nstd223human GRCh38 chr12: 118,054,469-123,705,974 , GRCh37.p13 chr12: 118,492,274-124,190,521 RPL11P5, RPL17P37, 159 more genes
    nsv6483876copy number variation1nstd223human GRCh38 chr12: 120,714,401-120,715,600 , GRCh37.p13 chr12: 121,152,204-121,153,403 UNC119B
    nsv6479046copy number variation1nstd223human GRCh38 chr12: 120,709,801-120,711,400 , GRCh37.p13 chr12: 121,147,604-121,149,203 UNC119B
    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
    nsv6475901copy number variation1nstd223human GRCh38 chr12: 120,642,301-120,710,200 , GRCh37.p13 chr12: 121,080,104-121,148,003 MLEC, CABP1, 2 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
    nsv5942460copy number variation1nstd209human GRCh38 chr12: 120,719,141-120,719,216 , GRCh37.p13 chr12: 121,156,944-121,157,019 UNC119B
    nsv5555463sequence alteration1nstd206human GRCh38 chr12: 120,561,097-121,398,447 , GRCh37.p13 chr12: 120,998,900-121,761,800 P2RX7, OASL, 27 more genes
    nsv5510443copy number variation1nstd206human GRCh38 chr12: 120,714,377-120,715,573 , GRCh37.p13 chr12: 121,152,180-121,153,376 UNC119B
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