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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7076787inversion1nstd229human GRCh38 chr12: 31,508,119-31,914,238 , GRCh37.p13 chr12: 31,661,053-32,067,172 RNU6-1069P, RPL31P50, 14 more genes
    nsv6930809copy number variation1nstd229human GRCh38 chr12: 31,771,844-31,831,730 , GRCh37.p13 chr12: 31,924,778-31,984,664 H3-5, RNU6-1069P, 1 more genes
    nsv6920277copy number variation1nstd229human GRCh38 chr12: 31,790,586-31,790,875 , GRCh37.p13 chr12: 31,943,520-31,943,809 H3-5
    nsv6621604copy number variation1nstd224human GRCh37 chr12: 31,819,105-31,945,000 , GRCh38.p12 chr12: 31,666,171-31,792,066 IFITM3P2, AMN1, 6 more genes
    nsv6473534copy number variation1nstd223human GRCh38 chr12: 31,792,504-31,793,241 , GRCh37.p13 chr12: 31,945,438-31,946,175 H3-5
    nsv6466639copy number variation1nstd223human GRCh38 chr12: 31,792,523-31,793,260 , GRCh37.p13 chr12: 31,945,457-31,946,194 H3-5
    nsv6132243copy number variation1nstd213human GRCh37 chr12: 31,860,000-34,000,001 , GRCh38.p12 chr12: 31,707,066-33,847,066 ASS1P14, BICD1, 26 more genes
    nsv6132242copy number variation1nstd213human GRCh37 chr12: 31,860,000-32,630,001 , GRCh38.p12 chr12: 31,707,066-32,477,067 BICD1, AMN1, 16 more genes
    nsv6132241copy number variation1nstd213human GRCh37 chr12: 31,410,000-34,000,001 , GRCh38.p12 chr12: 31,257,066-33,847,066 ASS1P14, BICD1, 39 more genes
    nsv6021782copy number variation1nstd212human GRCh38 chr12: 31,790,586-31,790,875 , GRCh37.p13 chr12: 31,943,520-31,943,809 H3-5
    nsv5923870copy number variation1nstd209human GRCh38 chr12: 31,790,586-31,790,874 , GRCh37.p13 chr12: 31,943,520-31,943,808 H3-5
    nsv5604249copy number variation1nstd207human GRCh38 chr12: 31,790,586-31,790,874 , GRCh37.p13 chr12: 31,943,520-31,943,808 H3-5
    nsv5512440copy number variation1nstd206human GRCh38 chr12: 31,792,485-31,793,287 , GRCh37.p13 chr12: 31,945,419-31,946,221 H3-5
    nsv5495508copy number variation1nstd206human GRCh38 chr12: 31,790,586-31,790,875 , GRCh37.p13 chr12: 31,943,520-31,943,809 H3-5
    nsv5355709translocation1nstd200human GRCh38 chr12: 31,790,586-31,790,586 , GRCh38 chr12: 31,790,875-31,790,875 , GRCh37.p13 chr12: 31,943,520-31,943,520 , GRCh37.p13 chr12: 31,943,809-31,943,809 H3-5
    nsv5310838copy number variation1nstd204human GRCh38.p13 chr12: 31,790,576-31,790,884 , GRCh37.p13 chr12: 31,943,510-31,943,818 H3-5
    nsv5264921copy number variation1nstd204human GRCh38.p13 chr12: 31,613,901-31,812,600 , GRCh37.p13 chr12: 31,766,835-31,965,534 , LOC105369724, 10 more genes
    nsv4974500copy number variation1nstd200human GRCh38 chr12: 31,792,422-31,793,335 , GRCh37.p13 chr12: 31,945,356-31,946,269 H3-5
    nsv4974499copy number variation1nstd200human GRCh38 chr12: 31,769,662-31,795,902 , GRCh37.p13 chr12: 31,922,596-31,948,836 , LOC107984470, 1 more genes
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