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Items: 1 to 20 of 228

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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
    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
    nsv7094066copy number variation1nstd102humanPathogenic GRCh37 chr13: 102,521,055-103,718,599 , GRCh38.p12 chr13: 101,868,705-103,066,249 FGF14-AS1, POGLUT2, 22 more genes
    nsv7077072inversion1nstd229human GRCh38 chr13: 102,676,907-102,874,566 , GRCh37.p13 chr13: 103,329,257-103,526,916 CCDC168, POGLUT2, 8 more genes
    nsv7075005inversion1nstd229human GRCh38 chr13: 102,729,066-102,760,008 , GRCh37.p13 chr13: 103,381,416-103,412,358 CCDC168, LOC105370337
    nsv7072178inversion1nstd229human GRCh38 chr13: 97,997,035-104,548,310 , GRCh37.p13 chr13: 98,649,289-105,200,661 RNU1-24P, DOCK9, 95 more genes
    nsv7070820inversion1nstd229human GRCh38 chr13: 102,729,062-102,753,214 , GRCh37.p13 chr13: 103,381,412-103,405,564 CCDC168
    nsv7068834inversion1nstd229human GRCh38 chr13: 102,755,110-102,755,173 , GRCh37.p13 chr13: 103,407,460-103,407,523 CCDC168
    nsv6952205copy number variation1nstd229human GRCh38 chr13: 102,742,763-102,742,949 , GRCh37.p13 chr13: 103,395,113-103,395,299 CCDC168
    nsv6945936copy number variation1nstd229human GRCh38 chr13: 102,668,892-102,872,921 , GRCh37.p13 chr13: 103,321,242-103,525,271 RNY5P8, TPP2, 8 more genes
    nsv6941026copy number variation1nstd229human GRCh38 chr13: 102,721,412-102,737,166 , GRCh37.p13 chr13: 103,373,762-103,389,516 CCDC168
    nsv6940818copy number variation1nstd229human GRCh38 chr13: 102,746,642-102,752,592 , GRCh37.p13 chr13: 103,398,992-103,404,942 CCDC168
    nsv6638047copy number variation1nstd102humanPathogenic GRCh37 chr13: 75,268,539-115,107,733 , GRCh38.p12 chr13: 74,694,402-114,342,258 CUL4A, LOC105370373, 488 more genes
    nsv6637615copy number variation1nstd102humanPathogenic GRCh37 chr13: 93,535,335-105,788,229 , GRCh38.p12 chr13: 92,883,082-105,135,878 SNORD13G, FTLP8, 162 more genes
    nsv6637531copy number variation1nstd102humanPathogenic GRCh37 chr13: 100,334,135-110,383,902 , GRCh38.p12 chr13: 99,681,881-109,731,555 ARGLU1, LINC00343, 101 more genes
    nsv6637400copy number variation1nstd102humanPathogenic GRCh37 chr13: 97,142,120-115,107,733 , GRCh38.p12 chr13: 96,489,866-114,342,258 LOC107984609, LINC00354, 265 more genes
    nsv6637217copy number variation1nstd102humanPathogenic GRCh37 chr13: 99,421,603-115,107,733 , GRCh38.p12 chr13: 98,769,349-114,342,258 LOC107984609, CLYBL-AS2, 231 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6494907copy number variation1nstd223human GRCh38 chr13: 102,737,701-102,741,500 , GRCh37.p13 chr13: 103,390,051-103,393,850 CCDC168
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