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Items: 1 to 20 of 259

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7069281inversion1nstd229human GRCh38 chr11: 107,936,485-114,400,629 , GRCh37.p13 chr11: 107,807,211-114,271,351 LRRC37A13P, POU2AF3, 121 more genes
    nsv6917908copy number variation1nstd229human GRCh38 chr11: 113,923,910-113,926,383 , GRCh37.p13 chr11: 113,794,632-113,797,105 HTR3B
    nsv6916023copy number variation1nstd229human GRCh38 chr11: 113,947,261-113,947,570 , GRCh37.p13 chr11: 113,817,983-113,818,292 HTR3B
    nsv6913906copy number variation1nstd229human GRCh38 chr11: 113,935,089-113,935,460 , GRCh37.p13 chr11: 113,805,811-113,806,182 HTR3B
    nsv6913845copy number variation1nstd229human GRCh38 chr11: 113,942,218-113,942,401 , GRCh37.p13 chr11: 113,812,940-113,813,123 HTR3B
    nsv6913821copy number variation1nstd229human GRCh38 chr11: 113,904,827-113,904,888 , GRCh37.p13 chr11: 113,775,549-113,775,610 HTR3B
    nsv6911962copy number variation1nstd229human GRCh38 chr11: 113,892,262-113,903,700 , GRCh37.p13 chr11: 113,762,984-113,774,422 HTR3B
    nsv6898823copy number variation1nstd229human GRCh38 chr11: 113,930,491-113,933,129 , GRCh37.p13 chr11: 113,801,213-113,803,851 HTR3B
    nsv6637811copy number variation1nstd102humanPathogenic GRCh37 chr11: 109,328,787-116,414,966 , GRCh38.p12 chr11: 109,458,061-116,544,249 LOC102723966, NXPE4, 129 more genes
    nsv6620799copy number variation1nstd224human GRCh37 chr11: 113,813,713-113,879,251 , GRCh38.p12 chr11: 113,942,991-114,008,529 HTR3B, HTR3A
    nsv6592462inversion1nstd223human GRCh38 chr11: 113,909,823-113,910,602 , GRCh37.p13 chr11: 113,780,545-113,781,324 HTR3B
    nsv6590616inversion1nstd223human GRCh38 chr11: 113,919,799-113,920,302 , GRCh37.p13 chr11: 113,790,521-113,791,024 HTR3B
    nsv6586218inversion1nstd223human GRCh38 chr11: 107,936,497-114,408,912 , GRCh37.p13 chr11: 107,807,223-114,279,634 LOC107984390, ATF4P4, 121 more genes
    nsv6475412copy number variation1nstd223human GRCh38 chr11: 113,925,445-113,926,687 , GRCh37.p13 chr11: 113,796,167-113,797,409 HTR3B
    nsv6471184copy number variation1nstd223human GRCh38 chr11: 113,935,087-113,935,460 , GRCh37.p13 chr11: 113,805,809-113,806,182 HTR3B
    nsv6465984copy number variation1nstd223human GRCh38 chr11: 113,920,314-113,922,481 , GRCh37.p13 chr11: 113,791,036-113,793,203 HTR3B
    nsv6460312copy number variation1nstd223human GRCh38 chr11: 113,934,810-113,935,455 , GRCh37.p13 chr11: 113,805,532-113,806,177 HTR3B
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6291074copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,375,478-128,785,742 , GRCh38.p12 chr11: 112,504,755-128,915,847 ZW10, MPZL2, 378 more genes
    nsv6290834copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,422,071-118,022,671 , GRCh38.p12 chr11: 85,711,028-118,151,956 CARD17P, RNA5SP350, 480 more genes
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