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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137191copy number variation1nstd102humanPathogenic GRCh37 chr1: 1,957,148-6,553,454 , GRCh38.p12 chr1: 2,025,709-6,493,394 LOC102724429, TNFRSF14, 86 more genes
    nsv7137045copy number variation1nstd102humanPathogenic GRCh37 chr1: 536,777-6,012,896 , GRCh38.p12 chr1: 601,397-5,952,836 MIR200B, LOC105378608, 172 more genes
    nsv7099173copy number variation1nstd231human GRCh38.p12 chr1: 3,521,699-3,692,482 , GRCh37 chr1: 3,438,263-3,609,046 MEGF6, TP73, 5 more genes
    nsv7098948copy number variation1nstd102humanUncertain significance GRCh38 chr1: 2,518,272-4,413,203 , GRCh37.p13 chr1: 2,449,711-4,473,263 LOC107984904, DFFB, 46 more genes
    nsv7058041inversion1nstd229human GRCh38 chr1: 1,845,355-9,534,096 , GRCh37.p13 chr1: 1,776,794-9,594,155 RPL37P9, TMEM52, 152 more genes
    nsv7054534inversion1nstd229human GRCh38 chr1: 2,972,403-10,562,308 , GRCh37.p13 chr1: 2,888,967-10,622,365 RN7SL731P, LOC105376682, 145 more genes
    nsv7051203inversion1nstd229human GRCh38 chr1: 2,476,867-3,696,891 , GRCh37.p13 chr1: 2,408,306-3,613,455 TP73, PRXL2B, 33 more genes
    nsv6649300copy number variation1nstd229human GRCh38 chr1: 3,531,301-3,590,900 , GRCh37.p13 chr1: 3,447,865-3,507,464 LOC105378608, MIR551A, 1 more genes
    nsv6649215copy number variation1nstd229human GRCh38 chr1: 3,532,130-4,419,144 , GRCh37.p13 chr1: 3,448,694-4,479,204 LINC02780, MIR551A, 19 more genes
    nsv6649200copy number variation1nstd229human GRCh38 chr1: 3,507,901-3,636,000 , GRCh37.p13 chr1: 3,424,465-3,552,564 WRAP73, TPRG1L, 3 more genes
    nsv6648783copy number variation1nstd229human GRCh38 chr1: 3,557,253-4,081,288 , GRCh37.p13 chr1: 3,473,817-4,141,348 LINC02780, MEGF6, 16 more genes
    nsv6647879copy number variation1nstd229human GRCh38 chr1: 2,800,201-3,815,100 , GRCh37.p13 chr1: 2,716,766-3,731,664 CEP104, PRDM16-DT, 22 more genes
    nsv6637093copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897 VWA1, CEP104, 311 more genes
    nsv6637067copy number variation1nstd102humanUncertain significance GRCh37 chr1: 2,974,212-4,408,415 , GRCh38.p12 chr1: 3,057,648-4,348,355 LRRC47, LOC105378605, 27 more genes
    nsv6636408copy number variation1nstd102humanUncertain significance GRCh37 chr1: 2,194,087-4,738,355 , GRCh38.p12 chr1: 2,262,648-4,678,295 LINC01777, LOC105378606, 55 more genes
    nsv6636399copy number variation1nstd102humanPathogenic GRCh37 chr1: 2,173,570-5,023,430 , GRCh38.p12 chr1: 2,242,131-4,963,370 LOC105378602, MORN1, 55 more genes
    nsv6635898copy number variation1nstd227human GRCh38.p12 chr1: 3,451,579-3,675,623 , GRCh37 chr1: 3,368,143-3,592,187 MEGF6, TP73, 6 more genes
    nsv6635782copy number variation1nstd227human GRCh38.p12 chr1: 3,462,371-3,587,509 , GRCh37 chr1: 3,378,935-3,504,073 MEGF6, ARHGEF16, 2 more genes
    nsv6635747copy number variation2nstd227human GRCh38.p12 chr1: 3,465,134-3,732,998 , GRCh37 chr1: 3,381,698-3,649,562 MEGF6, TP73, 6 more genes
    nsv6635312copy number variation1nstd227human GRCh38.p12 chr1: 3,465,134-3,675,623 , GRCh37 chr1: 3,381,698-3,592,187 MEGF6, TP73, 6 more genes
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