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Items: 1 to 20 of 121

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5916339copy number variation1nstd209human GRCh38 chr10: 96,354,652-96,354,923 , GRCh37.p13 chr10: 98,114,409-98,114,680 OPALIN
    nsv5914261copy number variation1nstd209human GRCh38 chr10: 96,349,046-96,349,100 , GRCh37.p13 chr10: 98,108,803-98,108,857 OPALIN
    nsv5561747sequence alteration1nstd206human GRCh38 chr10: 96,342,129-96,342,150 , GRCh37.p13 chr10: 98,101,886-98,101,907 OPALIN
    nsv5539607insertion1nstd206human GRCh38 chr10: 96,342,129-96,342,129 , GRCh37.p13 chr10: 98,101,886-98,101,886 OPALIN
    nsv5486178copy number variation1nstd206human GRCh38 chr10: 96,354,654-96,354,924 , GRCh37.p13 chr10: 98,114,411-98,114,681 OPALIN
    nsv5484335copy number variation1nstd206human GRCh38 chr10: 96,346,595-96,346,790 , GRCh37.p13 chr10: 98,106,352-98,106,547 OPALIN
    nsv5479276copy number variation1nstd206human GRCh38 chr10: 96,351,671-96,351,937 , GRCh37.p13 chr10: 98,111,428-98,111,694 OPALIN
    nsv5474698copy number variation1nstd206human GRCh38 chr10: 96,347,715-96,350,953 , GRCh37.p13 chr10: 98,107,472-98,110,710 OPALIN
    nsv5348016translocation1nstd200human GRCh38 chr10: 96,354,924-96,354,924 , GRCh38 chr10: 96,354,654-96,354,654 , GRCh37.p13 chr10: 98,114,411-98,114,411 , GRCh37.p13 chr10: 98,114,681-98,114,681 OPALIN
    nsv5341404translocation1nstd200human GRCh37 chr10: 98,114,681-98,114,681 , GRCh37 chr10: 98,114,411-98,114,411 , GRCh38.p12 chr10: 96,354,654-96,354,654 , GRCh38.p12 chr10: 96,354,924-96,354,924 OPALIN
    nsv4986818copy number variation1nstd200human GRCh38 chr10: 96,346,595-96,346,790 , GRCh37.p13 chr10: 98,106,352-98,106,547 OPALIN
    nsv4494318mobile element insertion1nstd166human GRCh37.p13 chr10: 98,109,842-98,109,842 , GRCh38.p12 chr10: 96,350,085-96,350,085 OPALIN
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4325673inversion1nstd166human GRCh37.p13 chr10: 92,228,734-107,785,320 , GRCh38.p12 chr10: 90,468,977-106,025,562 , COX15, 323 more genes
    nsv4191112copy number variation1nstd166human GRCh37.p13 chr10: 98,104,319-98,104,781 , GRCh38.p12 chr10: 96,344,562-96,345,024 OPALIN
    nsv4190431copy number variation1nstd166human GRCh37.p13 chr10: 98,114,411-98,114,811 , GRCh38.p12 chr10: 96,354,654-96,355,054 OPALIN
    nsv4183147copy number variation1nstd166human GRCh37.p13 chr10: 98,113,911-98,114,681 , GRCh38.p12 chr10: 96,354,154-96,354,924 OPALIN
    nsv3920295copy number variation1nstd102humanPathogenic NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422 EIF2S2P3, CYP17A1-AS1, 895 more genes
    nsv3912487copy number variation1nstd102humanPathogenic GRCh37 chr10: 94,386,437-99,514,859 , GRCh38 chr10: 92,626,680-97,755,102 , NCBI36 chr10: 94,376,417-99,504,849 ENTPD1-AS1, PLCE1, 105 more genes
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