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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5914382copy number variation1nstd209human GRCh38 chr10: 27,312,316-36,846,398 , GRCh37.p13 chr10: 27,601,245-37,135,326 , RN7SL241P, 160 more genes
    nsv5484184copy number variation1nstd206human GRCh38 chr10: 31,307,981-31,308,036 , GRCh37.p13 chr10: 31,596,910-31,596,965 ZEB1-AS1
    nsv4674831copy number variation1nstd102humanUncertain significance GRCh37 chr10: 31,548,044-32,172,367 , GRCh38.p12 chr10: 31,259,115-31,883,439 MACORIS, RNA5SP309, 8 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4179856copy number variation1nstd166human GRCh37.p13 chr10: 31,609,765-31,609,898 , GRCh38.p12 chr10: 31,320,836-31,320,969 ZEB1-AS1, ZEB1
    nsv4178471copy number variation1nstd166human GRCh37.p13 chr10: 31,576,000-31,595,100 , GRCh38.p12 chr10: 31,287,071-31,306,171 ZEB1-AS1
    nsv3965065insertion1nstd168human GRCh38 chr10: 31,289,957-31,343,050 , GRCh37.p13 chr10: 31,578,886-31,631,979 ZEB1-AS1, ZEB1
    nsv3922922copy number variation1nstd102humanUncertain significance NCBI36 chr10: 31,554,392-31,722,562 , GRCh37.p13 chr10: 31,514,386-31,682,556 , GRCh38.p12 chr10: 31,225,457-31,393,627 SPTLC1P1, ZEB1, 4 more genes
    nsv3920796copy number variation1nstd102humanPathogenic NCBI36 chr10: 62,842-35,729,127 , GRCh37.p13 chr10: 72,842-35,689,121 , GRCh38.p12 chr10: 26,906-35,400,193 EPC1-AS1, RNU6-452P, 559 more genes
    nsv3920598copy number variation1nstd102humanBenign NCBI36 chr10: 4,636,926-47,125,152 , GRCh38 chr10: 4,604,734-48,074,662 , GRCh37 chr10: 4,646,926-47,531,169 LOC100420467, LOC105376474, 709 more genes
    nsv3911634copy number variation1nstd102humanLikely pathogenic NCBI36 chr10: 19,417,096-33,061,227 , GRCh37 chr10: 19,377,090-33,021,221 , GRCh38 chr10: 19,088,161-32,732,293 BMI1, CCND3P1, 221 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 LOC100419870, LOC102724439, 2105 more genes
    nsv3904390copy number variation1nstd102humanPathogenic GRCh37 chr10: 100,026-50,961,640 , GRCh38.p12 chr10: 54,086-49,753,594 LINC00700, LINC02881, 806 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 ANXA11, EDRF1-DT, 2085 more genes
    nsv3895497copy number variation1nstd102humanPathogenic GRCh37 chr10: 31,425,682-32,599,180 , GRCh38.p12 chr10: 31,136,753-32,310,252 LOC107984219, LOC105376485, 21 more genes
    nsv3891958copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414 TUBB8, PPP2R2D, 2085 more genes
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 AGAP14P, LOC100505502, 2097 more genes
    nsv3167822copy number variation1nstd158human GRCh37 chr10: 31,159,932-31,852,201 , GRCh38.p12 chr10: 30,871,003-31,563,273 ZEB1, ZNF438, 9 more genes
    nsv3146290copy number variation1nstd151human GRCh37 chr10: 30,727,865-31,610,464 , GRCh38.p12 chr10: 30,438,936-31,321,535 MAP3K8, RNA5SP309, 15 more genes
    nsv1555834short tandem repeat3nstd128human GRCh37 chr10: 31,600,959-31,600,973 , GRCh38.p12 chr10: 31,312,030-31,312,044 ZEB1-AS1
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