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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7098887copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,249,133-97,616,970 , GRCh38.p12 chr10: 91,489,376-95,857,213 LGI1, LOC107984257, 79 more genes
    nsv6894002copy number variation1nstd229human GRCh38 chr10: 93,580,901-93,588,400 , GRCh37.p13 chr10: 95,340,658-95,348,157 FFAR4
    nsv6888317copy number variation1nstd229human GRCh38 chr10: 93,582,201-93,590,300 , GRCh37.p13 chr10: 95,341,958-95,350,057 RBP4, FFAR4
    nsv6878687copy number variation1nstd229human GRCh38 chr10: 93,571,486-93,571,939 , GRCh37.p13 chr10: 95,331,243-95,331,696 FFAR4
    nsv6637868copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,823,147-96,056,941 , GRCh38.p12 chr10: 88,063,390-94,297,184 RPS27P1, RNLS, 118 more genes
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5702794mobile element insertion2nstd211human GRCh38 chr10: 93,575,172-93,575,172 , GRCh37.p13 chr10: 95,334,929-95,334,929 FFAR4
    nsv5398389mobile element insertion1nstd206human GRCh38 chr10: 93,575,172-93,575,223 , GRCh37.p13 chr10: 95,334,929-95,334,980 FFAR4
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4986717copy number variation1nstd200human GRCh38 chr10: 93,581,989-93,582,117 , GRCh37.p13 chr10: 95,341,746-95,341,874 FFAR4
    nsv4841855copy number variation1nstd200human GRCh37 chr10: 95,340,624-95,348,166 , GRCh38.p12 chr10: 93,580,867-93,588,409 FFAR4
    nsv4837710copy number variation1nstd200human GRCh37 chr10: 95,341,746-95,341,874 , GRCh38.p12 chr10: 93,581,989-93,582,117 FFAR4
    nsv4682030copy number variation2nstd102humanPathogenic GRCh37 chr10: 94,921,066-95,557,580 , GRCh38.p12 chr10: 93,161,309-93,797,823 LGI1, LOC105378437, 11 more genes
    nsv4675093copy number variation1nstd102humanUncertain significance GRCh37 chr10: 95,234,481-95,431,148 , GRCh38.p12 chr10: 93,474,724-93,671,391 MYOF, CEP55, 6 more genes
    nsv4348834copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 94,393,383-97,219,175 , GRCh38.p12 chr10: 92,633,626-95,459,418 CYP2C19, CYP2C8, 51 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4325673inversion1nstd166human GRCh37.p13 chr10: 92,228,734-107,785,320 , GRCh38.p12 chr10: 90,468,977-106,025,562 , COX15, 323 more genes
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