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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141469insertion1nstd232human GRCh37.p13 chr9: 138,650,122-138,650,122 , GRCh38.p12 chr9: 135,758,276-135,758,276 KCNT1
    nsv7098438copy number variation1nstd102humanUncertain significance GRCh37 chr9: 138,606,403-138,606,586 , GRCh38.p12 chr9: 135,714,557-135,714,740 KCNT1
    nsv7098070copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr9: 138,392,557-141,016,451 , GRCh38.p12 chr9: 135,500,711-138,121,999 STPG3-AS1, CACNA1B-AS1, 132 more genes
    nsv7098066copy number variation4nstd102humanUncertain significance GRCh37 chr9: 135,139,626-140,034,216 , GRCh38.p12 chr9: 132,264,239-137,139,764 LINC02692, SNORD141A, 181 more genes
    nsv7097702copy number variation1nstd102humanUncertain significance GRCh37 chr9: 138,641,924-138,649,247 , GRCh38.p12 chr9: 135,750,078-135,757,401 KCNT1
    nsv7097697copy number variation1nstd102humanUncertain significance GRCh37 chr9: 136,218,768-141,016,451 , GRCh38.p12 chr9: 133,351,913-138,121,999 LOC105376326, LOC107987143, 186 more genes
    nsv7097690copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,087,402-141,016,451 , GRCh38.p12 chr9: 128,325,123-138,121,999 REXO4, TOR1B, 324 more genes
    nsv7093414copy number variation1nstd102humanPathogenic GRCh38 chr9: 134,932,722-137,269,957 , GRCh37.p13 chr9: 137,824,568-140,164,409 LHX3, FUT7, 121 more genes
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv7075229inversion1nstd229human GRCh38 chr9: 135,680,265-135,718,103 , GRCh37.p13 chr9: 138,572,111-138,609,949 KCNT1, LOC105376317, 1 more genes
    nsv7075196inversion1nstd229human GRCh38 chr9: 130,990,409-137,053,229 , GRCh37.p13 chr9: 133,865,796-139,947,681 LINC02907, LCN1, 196 more genes
    nsv7059760inversion1nstd229human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 LCN10, RAPGEF1, 196 more genes
    nsv6896611copy number variation1nstd229human GRCh38 chr9: 135,758,052-135,758,139 , GRCh37.p13 chr9: 138,649,898-138,649,985 KCNT1
    nsv6895705copy number variation1nstd229human GRCh38 chr9: 135,717,403-135,721,248 , GRCh37.p13 chr9: 138,609,249-138,613,094 KCNT1
    nsv6894123copy number variation1nstd229human GRCh38 chr9: 135,710,366-135,710,777 , GRCh37.p13 chr9: 138,602,212-138,602,623 KCNT1
    nsv6891003copy number variation1nstd229human GRCh38 chr9: 135,597,201-135,718,100 , GRCh37.p13 chr9: 138,489,047-138,609,946 LOC102723971, LOC105376317, 5 more genes
    nsv6890679copy number variation1nstd229human GRCh38 chr9: 135,756,893-135,763,915 , GRCh37.p13 chr9: 138,648,739-138,655,761 KCNT1
    nsv6888164copy number variation1nstd229human GRCh38 chr9: 135,723,870-135,724,058 , GRCh37.p13 chr9: 138,615,716-138,615,904 KCNT1
    nsv6887959copy number variation1nstd229human GRCh38 chr9: 135,743,792-135,748,629 , GRCh37.p13 chr9: 138,635,638-138,640,475 KCNT1
    nsv6886919copy number variation1nstd229human GRCh38 chr9: 135,789,062-135,789,130 , GRCh37.p13 chr9: 138,680,908-138,680,976 LOC107987140, KCNT1
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