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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7046399inversion1nstd229human GRCh38 chr7: 66,773-207,605 , GRCh37.p13 chr7: 66,773-207,605 LOC101929756, LOC105375115, 6 more genes
    nsv6816945copy number variation1nstd229human GRCh38 chr7: 63,601-119,900 , GRCh37.p13 chr7: 63,601-119,900 LOC105375113, LOC101929756, 1 more genes
    nsv6816660copy number variation1nstd229human GRCh38 chr7: 60,123-115,432 , GRCh37.p13 chr7: 60,123-115,432 LOC105375113, LOC101929756, 1 more genes
    nsv6816123copy number variation1nstd229human GRCh38 chr7: 45,102-189,606 , GRCh37.p13 chr7: 45,102-189,606 LINC03015, LOC105375115, 5 more genes
    nsv6812278copy number variation1nstd229human GRCh38 chr7: 67,901-108,900 , GRCh37.p13 chr7: 67,901-108,900 LOC105375113, LOC101929756
    nsv6811835copy number variation1nstd229human GRCh38 chr7: 50,901-140,400 , GRCh37.p13 chr7: 50,901-140,400 LOC101929756, LOC105375113, 1 more genes
    nsv6807441copy number variation1nstd229human GRCh38 chr7: 64,763-302,139 , GRCh37.p13 chr7: 64,763-342,105 LINC03015, LOC101929756, 8 more genes
    nsv6807224copy number variation1nstd229human GRCh38 chr7: 55,930-97,907 , GRCh37.p13 chr7: 55,930-97,907 LOC101929756, LOC105375113
    nsv6805883copy number variation1nstd229human GRCh38 chr7: 45,924-82,002 , GRCh37.p13 chr7: 45,924-82,002 LOC105375113, LOC101929756
    nsv6805656copy number variation1nstd229human GRCh38 chr7: 66,663-287,397 , GRCh37.p13 chr7: 66,663-327,363 LOC105375116, FAM20C, 6 more genes
    nsv6798924copy number variation1nstd229human GRCh38 chr7: 62,603-248,832 , GRCh37.p13 chr7: 62,603-288,798 LOC105375115, LOC101929756, 6 more genes
    nsv6798548copy number variation1nstd229human GRCh38 chr7: 72,694-72,720 , GRCh37.p13 chr7: 72,694-72,720 LOC105375113
    nsv6636881copy number variation1nstd102humanUncertain significance GRCh37 chr7: 43,361-704,573 , GRCh38.p12 chr7: 43,361-664,936 LOC116435278, LOC105375115, 18 more genes
    nsv6635583copy number variation2nstd227human GRCh37 chr7: 44,935-68,920 , GRCh38.p12 chr7: 44,935-68,920 , GRCh38.p12 chr7|NT_187558.1: 1,034-25,019 , GRCh38.p12 chr7|NT_187653.1: 37,256-61,241 LOC105375113
    nsv6634885copy number variation1nstd227human GRCh37 chr7: 44,935-194,247 , GRCh38.p12 chr7: 44,935-194,247 , GRCh38.p12 chr7|NT_187558.1: 1,034-153,651 , GRCh38.p12 chr7|NT_187653.1: 37,256-186,568 FAM20C, LINC03014, 6 more genes
    nsv6634397copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-19,485,604 , GRCh38.p12 chr7: 43,360-19,445,981 DNAAF5, FSCN1, 277 more genes
    nsv6634339copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-9,649,794 , GRCh38.p12 chr7: 43,360-9,610,164 MRM2, FOXL3, 182 more genes
    nsv6632094copy number variation1nstd224human GRCh37 chr7: 44,935-96,163 , GRCh38.p12 chr7: 44,935-96,163 , GRCh38.p12 chr7|NT_187558.1: 1,034-52,262 , GRCh38.p12 chr7|NT_187653.1: 37,256-88,484 LOC101929756, LOC105375113
    nsv6632091copy number variation1nstd224human GRCh37 chr7: 44,935-102,355 , GRCh38.p12 chr7: 44,935-102,355 , GRCh38.p12 chr7|NT_187558.1: 1,034-58,454 , GRCh38.p12 chr7|NT_187653.1: 37,256-94,676 LOC105375113, LOC101929756
    nsv6632090copy number variation1nstd224human GRCh37 chr7: 43,748-72,375 , GRCh38.p12 chr7: 43,748-72,375 , GRCh38.p12 chr7|NT_187558.1: 1-28,474 , GRCh38.p12 chr7|NT_187653.1: 36,069-64,696 LOC105375113
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