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Items: 1 to 20 of 93

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094183copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,146,421-75,283,128 , GRCh38.p12 chr11: 71,435,375-75,572,083 LOC112268078, LRTOMT, 142 more genes
    nsv7075540inversion1nstd229human GRCh38 chr11: 67,968,443-71,626,784 , GRCh37.p13 chr11: 67,735,914-71,337,830 S100A11P3, CCND1, 76 more genes
    nsv7073207inversion1nstd229human GRCh38 chr11: 71,538,472-71,581,296 , GRCh37.p13 chr11: 71,249,518-71,292,342 KRTAP5-9, KRTAP5-10, 4 more genes
    nsv6917532copy number variation1nstd229human GRCh38 chr11: 71,582,771-71,582,814 , GRCh37.p13 chr11: 71,293,817-71,293,860 KRTAP5-11
    nsv6912715copy number variation1nstd229human GRCh38 chr11: 71,563,101-71,654,600 , GRCh37.p13 chr11: 71,274,147-71,365,646 LOC645544, OR7E87P, 6 more genes
    nsv6908275copy number variation1nstd229human GRCh38 chr11: 71,281,500-72,194,614 , GRCh37.p13 chr11: 71,088,949-71,905,658 DEFB130C, ANAPC15, 40 more genes
    nsv6902473copy number variation1nstd229human GRCh38 chr11: 71,579,401-71,581,300 , GRCh37.p13 chr11: 71,290,447-71,292,346 KRTAP5-14P, KRTAP5-11
    nsv6901386copy number variation1nstd229human GRCh38 chr11: 71,579,201-71,581,100 , GRCh37.p13 chr11: 71,290,247-71,292,146 KRTAP5-11, KRTAP5-14P
    nsv6637237copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,051,703-71,655,505 , GRCh38.p12 chr11: 71,340,657-71,944,459 FAM86C1P, KRTAP5-7, 28 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6087181insertion1nstd212human GRCh38 chr11: 71,582,630-71,582,630 , GRCh37.p13 chr11: 71,293,676-71,293,676 KRTAP5-11
    nsv6033773copy number variation1nstd212human GRCh38 chr11: 71,580,466-71,580,528 , GRCh37.p13 chr11: 71,291,512-71,291,574 KRTAP5-14P, KRTAP5-11
    nsv5971271inversion1nstd209human GRCh37.p13 chr11: 71,290,831-71,301,785 , GRCh38 chr11: 71,579,785-71,590,739 KRTAP5-14P, KRTAP5-11
    nsv5505222copy number variation1nstd206human GRCh38 chr11: 71,582,494-71,582,560 , GRCh37.p13 chr11: 71,293,540-71,293,606 KRTAP5-11
    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
    nsv5125651mobile element insertion1nstd203human GRCh38 chr11: 71,579,970-71,579,986 , GRCh37.p13 chr11: 71,291,016-71,291,032 KRTAP5-11, KRTAP5-14P
    nsv4843541copy number variation1nstd200human GRCh37 chr11: 71,293,540-71,293,606 , GRCh38.p12 chr11: 71,582,494-71,582,560 KRTAP5-11
    nsv4681893copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,146,401-71,907,241 , GRCh38.p12 chr11: 71,435,355-72,196,197 OR7E128P, ZNF705EP, 39 more genes
    nsv4424589copy number variation1nstd174human GRCh37 chr11: 71,293,875-71,442,666 , GRCh38.p12 chr11: 71,582,829-71,731,620 OR7E4P, OR7E87P, 6 more genes
    nsv4415590copy number variation1nstd174human GRCh37 chr11: 71,293,875-71,619,923 , GRCh38.p12 chr11: 71,582,829-71,908,877 , FAM86C1P, 17 more genes
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