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Items: 1 to 20 of 351

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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
    nsv7053465inversion1nstd229human GRCh38 chr2: 207,147,046-207,157,246 , GRCh37.p13 chr2: 208,011,770-208,021,970 KLF7
    nsv7042341inversion1nstd229human GRCh38 chr2: 207,109,049-207,117,441 , GRCh37.p13 chr2: 207,973,773-207,982,165 MIR2355, KLF7
    nsv7040011inversion1nstd229human GRCh38 chr2: 206,913,241-207,274,391 , GRCh37.p13 chr2: 207,777,965-208,139,115 KLF7, MYOSLID, 6 more genes
    nsv7038468inversion1nstd229human GRCh38 chr2: 206,896,569-207,345,676 , GRCh37.p13 chr2: 207,761,293-208,210,400 KLF7, LINC01802, 7 more genes
    nsv6688578copy number variation1nstd229human GRCh38 chr2: 207,173,101-207,177,200 , GRCh37.p13 chr2: 208,037,825-208,041,924 KLF7
    nsv6681792copy number variation1nstd229human GRCh38 chr2: 207,173,031-207,177,182 , GRCh37.p13 chr2: 208,037,755-208,041,906 KLF7
    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
    nsv6353973copy number variation1nstd223human GRCh38 chr2: 207,085,570-207,086,294 , GRCh37.p13 chr2: 207,950,294-207,951,018 KLF7
    nsv6345274copy number variation1nstd223human GRCh38 chr2: 207,071,757-207,072,280 , GRCh37.p13 chr2: 207,936,481-207,937,004 KLF7
    nsv6345022copy number variation1nstd223human GRCh38 chr2: 206,375,924-207,087,017 , GRCh37.p13 chr2: 207,240,648-207,951,741 HNRNPA1P51, KLF7, 10 more genes
    nsv6338861copy number variation1nstd223human GRCh38 chr2: 207,173,031-207,177,181 , GRCh37.p13 chr2: 208,037,755-208,041,905 KLF7
    nsv6336256copy number variation1nstd223human GRCh38 chr2: 207,134,729-207,138,818 , GRCh37.p13 chr2: 207,999,453-208,003,542 KLF7
    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
    nsv6253291mobile element insertion1nstd215human GRCh38 chr2: 207,120,582-207,120,582 , GRCh37.p13 chr2: 207,985,306-207,985,306 KLF7
    nsv6253290mobile element insertion1nstd215human GRCh38 chr2: 207,112,178-207,112,178 , GRCh37.p13 chr2: 207,976,902-207,976,902 KLF7
    nsv6158030copy number variation1nstd214human GRCh38 chr2: 207,164,041-207,164,117 , GRCh37.p13 chr2: 208,028,765-208,028,841 KLF7
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