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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7076452inversion1nstd229human GRCh38 chr15: 70,935,934-70,936,012 , GRCh37.p13 chr15: 71,228,273-71,228,351 LRRC49
    nsv7073132inversion1nstd229human GRCh38 chr15: 70,946,092-70,946,120 , GRCh37.p13 chr15: 71,238,431-71,238,459 LRRC49
    nsv7070270inversion1nstd229human GRCh38 chr15: 70,870,846-78,233,029 , GRCh37.p13 chr15: 71,163,185-78,525,371 GOLGA6C, LOC102723657, 178 more genes
    nsv7069747inversion1nstd229human GRCh38 chr15: 65,994,863-75,247,978 , GRCh37.p13 chr15: 66,287,201-75,540,319 REC114, PARP6, 199 more genes
    nsv7069650inversion1nstd229human GRCh38 chr15: 70,907,182-70,916,400 , GRCh37.p13 chr15: 71,199,521-71,208,739 LRRC49
    nsv7061599inversion1nstd229human GRCh38 chr15: 71,004,055-71,004,197 , GRCh37.p13 chr15: 71,296,394-71,296,536 LRRC49
    nsv7059540inversion1nstd229human GRCh38 chr15: 70,999,345-71,011,266 , GRCh37.p13 chr15: 71,291,684-71,303,605 LRRC49
    nsv7059031inversion1nstd229human GRCh38 chr15: 70,160,153-73,809,878 , GRCh37.p13 chr15: 70,452,492-74,102,219 CD276, LOC107984716, 71 more genes
    nsv6976848copy number variation1nstd229human GRCh38 chr15: 70,999,255-71,059,863 , GRCh37.p13 chr15: 71,291,594-71,352,202 LRRC49
    nsv6975029copy number variation1nstd229human GRCh38 chr15: 70,937,916-71,146,347 , GRCh37.p13 chr15: 71,230,255-71,438,686 CT62, LOC105370886, 3 more genes
    nsv6970145copy number variation1nstd229human GRCh38 chr15: 70,978,191-70,978,209 , GRCh37.p13 chr15: 71,270,530-71,270,548 LRRC49
    nsv6969799copy number variation1nstd229human GRCh38 chr15: 70,930,875-70,931,677 , GRCh37.p13 chr15: 71,223,214-71,224,016 LRRC49
    nsv6966531copy number variation1nstd229human GRCh38 chr15: 70,939,001-71,146,400 , GRCh37.p13 chr15: 71,231,340-71,438,739 THSD4, CT62, 3 more genes
    nsv6965948copy number variation1nstd229human GRCh38 chr15: 71,034,432-71,034,599 , GRCh37.p13 chr15: 71,326,771-71,326,938 LRRC49
    nsv6965905copy number variation1nstd229human GRCh38 chr15: 71,005,724-71,007,884 , GRCh37.p13 chr15: 71,298,063-71,300,223 LRRC49
    nsv6965806copy number variation1nstd229human GRCh38 chr15: 71,025,601-71,030,900 , GRCh37.p13 chr15: 71,317,940-71,323,239 LRRC49
    nsv6965763copy number variation1nstd229human GRCh38 chr15: 71,006,824-71,007,001 , GRCh37.p13 chr15: 71,299,163-71,299,340 LRRC49
    nsv6964613copy number variation1nstd229human GRCh38 chr15: 70,938,201-70,944,600 , GRCh37.p13 chr15: 71,230,540-71,236,939 LRRC49
    nsv6962833copy number variation1nstd229human GRCh38 chr15: 70,888,246-70,895,302 , GRCh37.p13 chr15: 71,180,585-71,187,641 LRRC49, THAP10
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