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Items: 1 to 20 of 623

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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
    nsv7099172copy number variation1nstd231human GRCh38.p12 chr1: 3,353,612-3,503,571 , GRCh37 chr1: 3,270,176-3,420,135 MEGF6, ARHGEF16, 1 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
    nsv7042020inversion1nstd229human GRCh38 chr1: 3,480,883-3,481,135 , GRCh37.p13 chr1: 3,397,447-3,397,699 ARHGEF16
    nsv7040356inversion1nstd229human GRCh38 chr1: 3,480,981-3,481,590 , GRCh37.p13 chr1: 3,397,545-3,398,154 ARHGEF16
    nsv6649238copy number variation1nstd229human GRCh38 chr1: 3,477,801-3,485,900 , GRCh37.p13 chr1: 3,394,365-3,402,464 ARHGEF16
    nsv6649189copy number variation1nstd229human GRCh38 chr1: 3,478,147-3,481,400 , GRCh37.p13 chr1: 3,394,711-3,397,964 ARHGEF16
    nsv6649188copy number variation1nstd229human GRCh38 chr1: 3,477,101-3,485,900 , GRCh37.p13 chr1: 3,393,665-3,402,464 ARHGEF16
    nsv6649054copy number variation1nstd229human GRCh38 chr1: 3,471,066-3,472,844 , GRCh37.p13 chr1: 3,387,630-3,389,408 ARHGEF16
    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
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