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Items: 1 to 20 of 940

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148239copy number variation1nstd102humanPathogenic GRCh38 chr13: 98,343,655-110,990,677 , GRCh37.p13 chr13: 98,995,909-111,643,024 CLYBL-AS3, PPIAP24, 162 more genes
    nsv7098899copy number variation1nstd102humanPathogenic GRCh37 chr13: 95,675,427-105,286,434 , GRCh38.p12 chr13: 95,023,173-104,634,083 PCCA, LOC105370340, 131 more genes
    nsv7094414copy number variation1nstd102humanPathogenic GRCh37 chr13: 99,336,978-102,379,160 , GRCh38.p12 chr13: 98,684,724-101,726,810 MIR623, UBAC2-AS1, 51 more genes
    nsv7094230copy number variation3nstd102humanUncertain significance GRCh37 chr13: 100,038,233-103,718,599 , GRCh38.p12 chr13: 99,385,979-103,066,249 CLYBL-AS3, LOC107984615, 59 more genes
    nsv7094161copy number variation1nstd102humanUncertain significance GRCh37 chr13: 101,910,774-101,910,945 , GRCh38.p12 chr13: 101,258,423-101,258,594 NALCN
    nsv7093988copy number variation1nstd102humanPathogenic GRCh37 chr13: 101,936,264-101,944,737 , GRCh38.p12 chr13: 101,283,913-101,292,386 NALCN
    nsv7077440inversion1nstd229human GRCh38 chr13: 95,324,680-102,597,006 , GRCh37.p13 chr13: 95,976,934-103,249,356 RN7SL60P, RPL15P18, 111 more genes
    nsv7074117inversion1nstd229human GRCh38 chr13: 101,205,942-101,205,990 , GRCh37.p13 chr13: 101,858,293-101,858,341 NALCN
    nsv7072178inversion1nstd229human GRCh38 chr13: 97,997,035-104,548,310 , GRCh37.p13 chr13: 98,649,289-105,200,661 RNU1-24P, DOCK9, 95 more genes
    nsv7058633inversion1nstd229human GRCh38 chr13: 101,058,819-101,058,885 , GRCh37.p13 chr13: 101,711,171-101,711,237 NALCN-AS1, NALCN
    nsv6957858copy number variation1nstd229human GRCh38 chr13: 101,398,589-101,398,968 , GRCh37.p13 chr13: 102,050,940-102,051,319 NALCN
    nsv6957811copy number variation1nstd229human GRCh38 chr13: 101,204,574-101,211,194 , GRCh37.p13 chr13: 101,856,925-101,863,545 NALCN
    nsv6957233copy number variation1nstd229human GRCh38 chr13: 101,389,619-101,398,329 , GRCh37.p13 chr13: 102,041,970-102,050,680 NALCN
    nsv6957152copy number variation1nstd229human GRCh38 chr13: 101,096,641-101,100,957 , GRCh37.p13 chr13: 101,748,992-101,753,308 NALCN
    nsv6956872copy number variation1nstd229human GRCh38 chr13: 101,241,795-101,244,077 , GRCh37.p13 chr13: 101,894,146-101,896,428 NALCN
    nsv6955616copy number variation1nstd229human GRCh38 chr13: 101,114,965-101,120,087 , GRCh37.p13 chr13: 101,767,316-101,772,438 NALCN
    nsv6955184copy number variation1nstd229human GRCh38 chr13: 99,298,801-101,250,600 , GRCh37.p13 chr13: 99,951,055-101,902,951 PCCA-DT, HMGB3P4, 36 more genes
    nsv6953720copy number variation1nstd229human GRCh38 chr13: 101,347,580-101,353,556 , GRCh37.p13 chr13: 101,999,931-102,005,907 NALCN
    nsv6953638copy number variation1nstd229human GRCh38 chr13: 101,291,815-101,291,923 , GRCh37.p13 chr13: 101,944,166-101,944,274 NALCN
    nsv6952906copy number variation1nstd229human GRCh38 chr13: 101,204,601-101,211,200 , GRCh37.p13 chr13: 101,856,952-101,863,551 NALCN
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