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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5912867copy number variation1nstd209human GRCh38 chr10: 13,222,730-13,226,234 , GRCh37.p13 chr10: 13,264,730-13,268,234 UCMA
    nsv5863948copy number variation1nstd209human GRCh38 chr10: 13,222,724-13,224,597 , GRCh37.p13 chr10: 13,264,724-13,266,597 UCMA
    nsv5490272copy number variation1nstd206human GRCh38 chr10: 13,233,314-13,234,242 , GRCh37.p13 chr10: 13,275,314-13,276,242 UCMA
    nsv5486051copy number variation1nstd206human GRCh38 chr10: 13,227,991-13,228,545 , GRCh37.p13 chr10: 13,269,991-13,270,545 UCMA
    nsv5381768copy number variation1nstd102humanPathogenic GRCh37 chr10: 9,137,489-17,227,168 , GRCh38.p12 chr10: 9,095,526-17,185,169 PROSER2, C1QL3, 110 more genes
    nsv5347522translocation1nstd200human GRCh38 chr10: 13,234,242-13,234,242 , GRCh38 chr10: 13,233,314-13,233,314 , GRCh37.p13 chr10: 13,275,314-13,275,314 , GRCh37.p13 chr10: 13,276,242-13,276,242 UCMA
    nsv5343284translocation1nstd200human GRCh37 chr10: 13,275,314-13,275,314 , GRCh37 chr10: 13,276,242-13,276,242 , GRCh38.p12 chr10: 13,233,314-13,233,314 , GRCh38.p12 chr10: 13,234,242-13,234,242 UCMA
    nsv5311248copy number variation1nstd204human GRCh38.p13 chr10: 12,989,624-13,237,480 , GRCh37.p13 chr10: 13,031,624-13,279,480 OPTN, RNU6-6P, 7 more genes
    nsv5242532copy number variation1nstd204human GRCh37.p13 chr10: 13,031,601-13,279,500 , GRCh38.p13 chr10: 12,989,601-13,237,500 OPTN, RNU6-6P, 7 more genes
    nsv4831254copy number variation1nstd200human GRCh37 chr10: 13,264,758-13,268,235 , GRCh38.p12 chr10: 13,222,758-13,226,235 UCMA
    nsv4684253copy number variation1nstd102humanUncertain significance GRCh37 chr10: 12,805,430-13,306,566 , GRCh38.p12 chr10: 12,763,431-13,264,566 RPL5P25, SNRPGP5, 10 more genes
    nsv4610250copy number variation1nstd183human GRCh37 chr10: 13,275,325-13,276,262 , GRCh38.p12 chr10: 13,233,325-13,234,262 UCMA
    nsv4487243mobile element insertion1nstd166human GRCh37.p13 chr10: 13,275,106-13,275,106 , GRCh38.p12 chr10: 13,233,106-13,233,106 UCMA
    nsv4455607copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,026-15,273,144 , GRCh38.p12 chr10: 54,086-15,231,145 LOC105376357, LINC02649, 264 more genes
    nsv4430756copy number variation1nstd174human GRCh37 chr10: 13,258,936-13,261,768 , GRCh38.p12 chr10: 13,216,936-13,219,768 UCMA, RNU6-6P
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4189969copy number variation1nstd166human GRCh37.p13 chr10: 13,275,314-13,276,242 , GRCh38.p12 chr10: 13,233,314-13,234,242 UCMA
    nsv3970157copy number variation1nstd168human GRCh38 chr10: 13,192,265-13,256,583 , GRCh37.p13 chr10: 13,234,265-13,298,583 MCM10, UCMA, 1 more genes
    nsv3924406copy number variation1nstd102humanPathogenic GRCh38 chr10: 69,261-19,184,047 , GRCh37 chr10: 224,406-19,472,976 , NCBI36 chr10: 105,201-19,512,982 WDR37, LOC105376364, 302 more genes
    nsv3920796copy number variation1nstd102humanPathogenic NCBI36 chr10: 62,842-35,729,127 , GRCh37.p13 chr10: 72,842-35,689,121 , GRCh38.p12 chr10: 26,906-35,400,193 EPC1-AS1, RNU6-452P, 559 more genes
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