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Items: 1 to 20 of 242

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6717574copy number variation1nstd229human GRCh38 chr3: 14,389,375-14,402,401 , GRCh37.p13 chr3: 14,430,875-14,443,901 SLC6A6, RNA5SP124, 1 more genes
    nsv6716940copy number variation1nstd229human GRCh38 chr3: 14,238,801-14,635,300 , GRCh37.p13 chr3: 14,280,301-14,676,807 RNA5SP124, LOC105376960, 6 more genes
    nsv6715798copy number variation1nstd229human GRCh38 chr3: 14,424,920-14,425,658 , GRCh37.p13 chr3: 14,466,428-14,467,166 SLC6A6
    nsv6715312copy number variation1nstd229human GRCh38 chr3: 14,454,548-14,454,913 , GRCh37.p13 chr3: 14,496,056-14,496,421 SLC6A6
    nsv6714894copy number variation1nstd229human GRCh38 chr3: 14,064,301-14,499,300 , GRCh37.p13 chr3: 14,105,801-14,540,808 TMEM43, SLC6A6, 11 more genes
    nsv6708036copy number variation1nstd229human GRCh38 chr3: 14,436,540-14,436,582 , GRCh37.p13 chr3: 14,478,048-14,478,090 SLC6A6
    nsv6706828copy number variation1nstd229human GRCh38 chr3: 14,423,355-14,426,239 , GRCh37.p13 chr3: 14,464,863-14,467,747 SLC6A6
    nsv6702945copy number variation1nstd229human GRCh38 chr3: 14,415,469-14,421,810 , GRCh37.p13 chr3: 14,456,977-14,463,318 SLC6A6
    nsv6701641copy number variation1nstd229human GRCh38 chr3: 14,460,216-14,464,803 , GRCh37.p13 chr3: 14,501,724-14,506,311 SLC6A6
    nsv6700204copy number variation1nstd229human GRCh38 chr3: 14,428,524-14,443,219 , GRCh37.p13 chr3: 14,470,032-14,484,727 SLC6A6
    nsv6634367copy number variation1nstd102humanPathogenic GRCh37 chr3: 13,836,340-25,357,427 , GRCh38.p12 chr3: 13,794,843-25,315,936 TMEM43, SLC6A6, 132 more genes
    nsv6375262copy number variation1nstd223human GRCh38 chr3: 14,423,355-14,426,234 , GRCh37.p13 chr3: 14,464,863-14,467,742 SLC6A6
    nsv6360540copy number variation1nstd223human GRCh38 chr3: 14,415,469-14,421,810 , GRCh37.p13 chr3: 14,456,977-14,463,318 SLC6A6
    nsv6315249copy number variation1nstd102humanPathogenic GRCh38 chr3: 13,371,737-20,095,506 , GRCh37.p13 chr3: 13,413,237-20,136,998 RNU6-905P, PRR3P1, 99 more genes
    nsv6289801copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 14,406,477-14,509,088 , GRCh38.p12 chr3: 14,364,977-14,467,580 SLC6A6, RNA5SP124, 1 more genes
    nsv6253723mobile element insertion1nstd215human GRCh38 chr3: 14,430,827-14,430,827 , GRCh37.p13 chr3: 14,472,335-14,472,335 SLC6A6
    nsv5991417copy number variation1nstd212human GRCh38 chr3: 14,435,294-14,435,347 , GRCh37.p13 chr3: 14,476,802-14,476,855 SLC6A6
    nsv5948274insertion1nstd209human GRCh38 chr3: 14,427,134-14,427,134 , GRCh37.p13 chr3: 14,468,642-14,468,642 SLC6A6
    nsv5907327copy number variation1nstd209human GRCh38 chr3: 14,415,469-14,421,809 , GRCh37.p13 chr3: 14,456,977-14,463,317 SLC6A6
    nsv5835254copy number variation1nstd209human GRCh38 chr3: 14,415,474-14,420,982 , GRCh37.p13 chr3: 14,456,982-14,462,490 SLC6A6
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