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Items: 1 to 20 of 353

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094711copy number variation1nstd102humanUncertain significance GRCh37 chr15: 45,152,372-45,670,651 , GRCh38.p12 chr15: 44,860,174-45,378,453 TRH-GTG1-8, H3P39, 25 more genes
    nsv7094538copy number variation1nstd102humanUncertain significance GRCh37 chr15: 45,152,372-45,390,276 , GRCh38.p12 chr15: 44,860,174-45,098,078 LOC100129830, RNU1-119P, 11 more genes
    nsv7075144inversion1nstd229human GRCh38 chr15: 44,929,582-45,099,591 , GRCh37.p13 chr15: 45,221,780-45,391,789 LOC100422669, RNU1-78P, 7 more genes
    nsv7071814inversion1nstd229human GRCh38 chr15: 44,831,365-45,069,151 , GRCh37.p13 chr15: 45,123,563-45,361,349 RNU6-1108P, SORD2P, 11 more genes
    nsv7071359inversion1nstd229human GRCh38 chr15: 44,848,280-45,042,532 , GRCh37.p13 chr15: 45,140,478-45,334,730 RNU1-78P, RNU6-1332P, 10 more genes
    nsv7063642inversion1nstd229human GRCh38 chr15: 44,834,162-45,057,076 , GRCh37.p13 chr15: 45,126,360-45,349,274 LOC100129830, SORD, 11 more genes
    nsv7062358inversion1nstd229human GRCh38 chr15: 44,831,502-45,069,134 , GRCh37.p13 chr15: 45,123,700-45,361,332 LOC100129830, RNU6-966P, 11 more genes
    nsv7062340inversion1nstd229human GRCh38 chr15: 44,782,422-45,081,325 , GRCh37.p13 chr15: 45,074,620-45,373,523 SORD, RNU6-1332P, 11 more genes
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv7060857inversion1nstd229human GRCh38 chr15: 45,070,673-45,071,505 , GRCh37.p13 chr15: 45,362,871-45,363,703 SORD
    nsv6975026copy number variation1nstd229human GRCh38 chr15: 45,060,101-45,062,200 , GRCh37.p13 chr15: 45,352,299-45,354,398 SORD
    nsv6974228copy number variation1nstd229human GRCh38 chr15: 45,061,465-45,061,851 , GRCh37.p13 chr15: 45,353,663-45,354,049 SORD
    nsv6970947copy number variation1nstd229human GRCh38 chr15: 45,024,151-45,027,139 , GRCh37.p13 chr15: 45,316,349-45,319,337 SORD
    nsv6970122copy number variation1nstd229human GRCh38 chr15: 45,057,101-45,061,200 , GRCh37.p13 chr15: 45,349,299-45,353,398 SORD
    nsv6964488copy number variation1nstd229human GRCh38 chr15: 45,073,664-45,092,567 , GRCh37.p13 chr15: 45,365,862-45,384,765 SORD, DUOX2
    nsv6961575copy number variation1nstd229human GRCh38 chr15: 44,757,685-45,480,791 , GRCh37.p13 chr15: 45,049,883-45,772,989 SORD, C15orf48, 34 more genes
    nsv6623261copy number variation1nstd224human GRCh37 chr15: 45,017,726-45,387,741 , GRCh38.p12 chr15: 44,725,528-45,095,543 , GRCh38.p12 chr15|NT_187605.1: 48,896-244,917 SORD2P, LOC100129830, 14 more genes
    nsv6589130inversion1nstd223human GRCh38 chr15: 44,839,010-45,061,893 , GRCh37.p13 chr15: 45,131,208-45,354,091 RNU6-966P, LOC100420928, 11 more genes
    nsv6587937inversion1nstd223human GRCh38 chr15: 44,827,890-45,072,693 , GRCh37.p13 chr15: 45,120,088-45,364,891 SORD2P, TERB2, 11 more genes
    nsv6515202copy number variation1nstd223human GRCh38 chr15: 45,057,094-45,061,234 , GRCh37.p13 chr15: 45,349,292-45,353,432 SORD
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