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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980222inversion1nstd209human GRCh37.p13 chr11: 48,898,329-48,935,988 , GRCh38 chr11: 48,876,777-48,914,436 ANKRD33BP2, LOC100420449
    nsv5976205inversion1nstd209human GRCh38 chr11: 48,355,846-48,978,824 , GRCh37.p13 chr11: 48,377,398-49,000,376 , OR4C5, 17 more genes
    nsv5919272copy number variation1nstd209human GRCh38 chr11: 48,727,127-55,124,866 , GRCh37.p13 chr11: 48,748,679-54,892,342 , OR4C50P, 54 more genes
    nsv5668989inversion1nstd207human GRCh37.p13 chr11: 48,901,936-48,921,514 , GRCh38 chr11: 48,880,384-48,899,962 ANKRD33BP2
    nsv5508855copy number variation1nstd206human GRCh38 chr11: 48,356,000-48,949,500 , GRCh37.p13 chr11: 48,377,552-48,971,052 LOC100420449, OR4C2P, 15 more genes
    nsv5506322copy number variation1nstd206human GRCh38 chr11: 48,106,678-48,968,618 , GRCh37.p13 chr11: 48,128,230-48,990,170 , OR4X2, 24 more genes
    nsv5504254copy number variation1nstd206human GRCh38 chr11: 48,900,000-48,916,000 , GRCh37.p13 chr11: 48,921,552-48,937,552 ANKRD33BP2, LOC100420449
    nsv5499613copy number variation1nstd206human GRCh38 chr11: 48,896,500-48,960,000 , GRCh37.p13 chr11: 48,918,052-48,981,552 ANKRD33BP2, LOC100420449, 1 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5276966copy number variation1nstd204human GRCh38.p13 chr11: 48,901,228-48,902,930 , GRCh37.p13 chr11: 48,922,780-48,924,482 ANKRD33BP2
    nsv5263659copy number variation1nstd204human GRCh38.p13 chr11: 48,888,347-48,907,323 , GRCh37.p13 chr11: 48,909,899-48,928,875 LOC100420449, ANKRD33BP2
    nsv5260425copy number variation1nstd204human GRCh38.p13 chr11: 48,881,801-48,902,000 , GRCh37.p13 chr11: 48,903,353-48,923,552 ANKRD33BP2
    nsv4757869inversion1nstd199human GRCh37 chr11: 48,902,592-48,920,937 , GRCh38.p12 chr11: 48,881,040-48,899,385 ANKRD33BP2
    nsv4754709inversion1nstd199human GRCh37 chr11: 48,388,907-50,039,362 , GRCh38.p12 chr11: 48,367,355-50,080,208 , FOLH1, 47 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4730080inversion13nstd198human GRCh37.p13 chr11: 48,902,019-48,921,523 , GRCh38 chr11: 48,880,467-48,899,971 ANKRD33BP2
    nsv4728948copy number variation1nstd102humanLikely benign GRCh37 chr11: 48,242,702-49,562,051 , GRCh38.p12 chr11: 48,221,150-49,540,499 TRIM64C, OR4C9P, 36 more genes
    nsv4679508copy number variation1nstd189human GRCh37.p13 chr11: 48,028,344-55,363,340 , GRCh38.p12 chr11: 48,006,792-55,595,864 , FOLH1, 96 more genes
    nsv4636719copy number variation1nstd186human GRCh37 chr11: 48,881,700-48,935,000 , GRCh38.p12 chr11: 48,860,148-48,913,448 ANKRD33BP2, LOC100420449
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