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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141316copy number variation1nstd232human GRCh37.p13 chr15: 68,689,883-68,689,934 , GRCh38.p12 chr15: 68,397,544-68,397,595 ITGA11
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7074571inversion1nstd229human GRCh38 chr15: 68,414,052-68,415,984 , GRCh37.p13 chr15: 68,706,391-68,708,323 ITGA11
    nsv7069747inversion1nstd229human GRCh38 chr15: 65,994,863-75,247,978 , GRCh37.p13 chr15: 66,287,201-75,540,319 REC114, PARP6, 199 more genes
    nsv7064235inversion1nstd229human GRCh38 chr15: 68,177,132-69,135,262 , GRCh37.p13 chr15: 68,469,470-69,427,601 CORO2B, LOC105370873, 16 more genes
    nsv7063557inversion1nstd229human GRCh38 chr15: 68,148,341-69,105,455 , GRCh37.p13 chr15: 68,440,679-69,397,795 ITGA11, MIR4312, 16 more genes
    nsv7058734inversion1nstd229human GRCh38 chr15: 68,148,356-69,105,454 , GRCh37.p13 chr15: 68,440,694-69,397,794 LOC105370873, CORO2B, 16 more genes
    nsv6977763copy number variation1nstd229human GRCh38 chr15: 68,327,701-68,330,500 , GRCh37.p13 chr15: 68,620,039-68,622,838 ITGA11
    nsv6977020copy number variation1nstd229human GRCh38 chr15: 68,407,172-68,428,883 , GRCh37.p13 chr15: 68,699,511-68,721,222 ITGA11
    nsv6975313copy number variation1nstd229human GRCh38 chr15: 68,387,001-68,395,700 , GRCh37.p13 chr15: 68,679,340-68,688,039 ITGA11
    nsv6975192copy number variation1nstd229human GRCh38 chr15: 68,330,343-68,342,514 , GRCh37.p13 chr15: 68,622,681-68,634,852 ITGA11
    nsv6974782copy number variation1nstd229human GRCh38 chr15: 68,302,467-68,306,485 , GRCh37.p13 chr15: 68,594,805-68,598,823 ITGA11
    nsv6963126copy number variation1nstd229human GRCh38 chr15: 68,312,756-68,320,125 , GRCh37.p13 chr15: 68,605,094-68,612,463 ITGA11
    nsv6963125copy number variation1nstd229human GRCh38 chr15: 68,347,458-68,347,845 , GRCh37.p13 chr15: 68,639,796-68,640,183 ITGA11
    nsv6962891copy number variation1nstd229human GRCh38 chr15: 68,295,642-68,299,194 , GRCh37.p13 chr15: 68,587,980-68,591,532 ITGA11, FEM1B
    nsv6962216copy number variation1nstd229human GRCh38 chr15: 68,344,087-68,350,619 , GRCh37.p13 chr15: 68,636,425-68,642,957 ITGA11
    nsv6961664copy number variation1nstd229human GRCh38 chr15: 68,420,999-68,421,219 , GRCh37.p13 chr15: 68,713,338-68,713,558 ITGA11
    nsv6958448copy number variation1nstd229human GRCh38 chr15: 68,303,342-68,332,174 , GRCh37.p13 chr15: 68,595,680-68,624,512 ITGA11
    nsv6637804copy number variation1nstd102humanUncertain significance GRCh37 chr15: 68,593,993-69,070,537 , GRCh38.p12 chr15: 68,301,655-68,778,198 LOC105370873, CORO2B, 3 more genes
    nsv6513107copy number variation1nstd223human GRCh38 chr15: 68,344,087-68,350,615 , GRCh37.p13 chr15: 68,636,425-68,642,953 ITGA11
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