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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112768copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,984,696-46,405,042 , GRCh38.p12 chr5: 34,984,591-46,404,940 LIFR-AS1, FGF10-AS1, 137 more genes
    nsv5906337copy number variation1nstd209human GRCh38 chr5: 41,901,817-41,903,613 , GRCh37.p13 chr5: 41,901,919-41,903,715 RIMOC1
    nsv5842426copy number variation1nstd209human GRCh38 chr5: 41,901,837-41,903,636 , GRCh37.p13 chr5: 41,901,939-41,903,738 RIMOC1
    nsv5728321mobile element insertion1nstd211human GRCh38 chr5: 41,917,911-41,917,911 , GRCh37.p13 chr5: 41,918,013-41,918,013 FBXO4, RIMOC1
    nsv5581485copy number variation1nstd207human GRCh38 chr5: 41,901,817-41,903,613 , GRCh37.p13 chr5: 41,901,919-41,903,715 RIMOC1
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5459187copy number variation1nstd206human GRCh38 chr5: 41,868,742-41,962,064 , GRCh37.p13 chr5: 41,868,844-41,962,166 OXCT1, FBXO4, 6 more genes
    nsv5455821copy number variation1nstd206human GRCh38 chr5: 41,901,819-41,903,614 , GRCh37.p13 chr5: 41,901,921-41,903,716 RIMOC1
    nsv5381781copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,081,195-45,294,031 , GRCh38.p12 chr5: 29,081,088-45,293,929 ST3GAL5P1, LOC105374711, 213 more genes
    nsv5300478copy number variation1nstd204human GRCh38.p13 chr5: 41,901,816-41,903,615 , GRCh37.p13 chr5: 41,901,918-41,903,717 RIMOC1
    nsv5232320copy number variation1nstd204human GRCh38.p13 chr5: 41,901,837-41,903,636 , GRCh37.p13 chr5: 41,901,939-41,903,738 RIMOC1
    nsv5224425copy number variation1nstd204human GRCh38.p13 chr5: 41,901,801-41,903,600 , GRCh37.p13 chr5: 41,901,903-41,903,702 RIMOC1
    nsv4946834copy number variation1nstd200human GRCh38 chr5: 41,901,819-41,903,614 , GRCh37.p13 chr5: 41,901,921-41,903,716 RIMOC1
    nsv4946832copy number variation1nstd200human GRCh38 chr5: 41,879,700-42,913,282 , GRCh37.p13 chr5: 41,879,802-42,913,384 RPS2P22, SERBP1P6, 14 more genes
    nsv4802664copy number variation1nstd200human GRCh37 chr5: 41,901,921-41,903,716 , GRCh38.p12 chr5: 41,901,819-41,903,614 RIMOC1
    nsv4680426copy number variation1nstd189human GRCh37.p13 chr5: 37,623,394-42,403,769 , GRCh38.p12 chr5: 37,623,292-42,403,667 , C6, 65 more genes
    nsv4674231copy number variation1nstd102humanPathogenic GRCh37 chr5: 38,432,180-49,441,945 , GRCh38.p12 chr5: 38,432,078-50,146,111 RPSAP38, LOC105374746, 92 more genes
    nsv4662723copy number variation1nstd186human GRCh37 chr5: 41,901,889-41,903,717 , GRCh38.p12 chr5: 41,901,787-41,903,615 RIMOC1
    nsv4659361copy number variation1nstd186human GRCh37 chr5: 41,901,871-41,903,659 , GRCh38.p12 chr5: 41,901,769-41,903,557 RIMOC1
    nsv4647168copy number variation1nstd186human GRCh37 chr5: 41,901,908-41,903,715 , GRCh38.p12 chr5: 41,901,806-41,903,613 RIMOC1
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