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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv6688659copy number variation1nstd229human GRCh38 chr2: 206,160,365-206,160,428 , GRCh37.p13 chr2: 207,025,089-207,025,152 SNORA41, SNORD51, 1 more genes
    nsv6637127copy number variation1nstd102humanPathogenic GRCh37 chr2: 189,909,904-209,468,383 , GRCh38.p12 chr2: 189,045,178-208,603,658 LOC100421409, LOC100507443, 310 more genes
    nsv6315398copy number variation1nstd102humanPathogenic GRCh37 chr2: 185,697,659-213,002,074 , GRCh38.p12 chr2: 184,832,932-212,137,349 LOC107985785, MYO1B, 381 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313730copy number variation1nstd102humanPathogenic GRCh37 chr2: 200,851,079-209,054,267 , GRCh38.p12 chr2: 199,986,356-208,189,543 RN7SKP200, PIMREGP1, 179 more genes
    nsv6311631copy number variation1nstd102humanUncertain significance GRCh37 chr2: 203,420,070-211,811,277 , GRCh38.p12 chr2: 202,555,347-210,946,553 MIR3130-2, WDR12, 133 more genes
    nsv6290713copy number variation1nstd102humanUncertain significance GRCh37 chr2: 206,887,779-207,064,790 , GRCh38.p12 chr2: 206,023,055-206,200,066 , GRCh38.p12 chr2|NW_015495299.1: 132,073-309,084 EEF1B2, NDUFS1, 6 more genes
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5033412inversion1nstd200human GRCh38 chr2: 206,107,842-207,979,103 , GRCh37.p13 chr2: 206,972,566-208,843,827 ATP5POP1, MIR2355, 39 more genes
    nsv4913861copy number variation1nstd200human GRCh38 chr2: 206,037,358-206,205,364 , GRCh37.p13 chr2: 206,902,082-207,070,088 , INO80D, 8 more genes
    nsv4876881inversion1nstd200human GRCh37 chr2: 206,972,566-208,843,827 , GRCh38.p12 chr2: 206,107,842-207,979,103 CREB1, RN7SKP260, 39 more genes
    nsv4804566copy number variation1nstd200human GRCh37 chr2: 206,902,082-207,070,088 , GRCh38.p12 chr2: 206,037,358-206,205,364 , GRCh38.p12 chr2|NW_015495299.1: 146,376-314,382 , EEF1B2, 8 more genes
    nsv4769348copy number variation1nstd102humanUncertain significance GRCh37 chr2: 204,312,776-208,235,204 , GRCh38.p12 chr2: 203,448,053-207,370,480 PARD3B, DSTNP5, 50 more genes
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4728545copy number variation1nstd102humanPathogenic GRCh37 chr2: 204,445,619-212,580,788 , GRCh38.p12 chr2: 203,580,896-211,716,063 FASTKD2, MYL6BP1, 110 more genes
    nsv4715045copy number variation1nstd195human GRCh38.p12 chr2: 206,162,132-206,162,133 , GRCh37 chr2: 207,026,856-207,026,857 , GRCh38.p12 chr2|NW_015495299.1: 271,150-271,151 EEF1B2, SNORD51, 1 more genes
    nsv4674383copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,233,162-211,927,188 , GRCh38.p12 chr2: 162,376,652-211,062,464 SNORA41, LOC101929633, 663 more genes
    nsv4436532copy number variation1nstd102humanPathogenic GRCh37 chr2: 188,926,928-225,298,653 , GRCh38.p12 chr2: 188,062,201-224,433,936 MARS2, KRT18P19, 575 more genes
    nsv4390150copy number variation1nstd171human GRCh38.p12 chr2: 206,162,351-206,162,397 , GRCh37 chr2: 207,027,075-207,027,121 , GRCh38.p12 chr2|NW_015495299.1: 271,369-271,415 EEF1B2, SNORD51, 1 more genes
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