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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3151058copy number variation1estd209human GRCh37 chr11: 61,560,897-61,560,898 , GRCh38.p12 chr11: 61,793,425-61,793,426 FEN1
    nsv975935copy number variation97nstd82eastern lowland gorilla, Cross River gorilla, western lowland gorilla, Denisova hominin, human, pygmy chimpanzee, Pan troglodytes ellioti, Pan troglodytes schweinfurthii, Pan troglodytes troglodytes, Pan troglodytes verus, Sumatran orangutan, Bornean orangutan NCBI36 chr11: 61,319,815-61,320,459 , GRCh37.p13 chr11: 61,563,239-61,563,883 , GRCh38.p12 chr11: 61,795,767-61,796,411 FEN1
    esv2891090insertion1estd209human GRCh37 chr11: 61,563,203-61,563,203 , GRCh38.p12 chr11: 61,795,731-61,795,731 FEN1
    esv2891089insertion1estd209human GRCh37 chr11: 61,561,815-61,561,815 , GRCh38.p12 chr11: 61,794,343-61,794,343 FEN1
    esv1378896insertion1estd22human NCBI36 chr11: 61,318,405-61,318,405 , GRCh37.p13 chr11: 61,561,829-61,561,829 , GRCh38.p12 chr11: 61,794,357-61,794,357 FEN1
    nsv1588781short tandem repeat1nstd128human GRCh37 chr11: 61,561,417-61,561,452 , GRCh38.p12 chr11: 61,793,945-61,793,980 FEN1
    nsv1588175short tandem repeat3nstd128human GRCh37 chr11: 61,561,816-61,561,829 , GRCh38.p12 chr11: 61,794,344-61,794,357 FEN1
    esv3809459copy number variation1estd192human GRCh37 chr11: 61,563,594-61,566,694 , GRCh38.p12 chr11: 61,796,122-61,799,222 FEN1, FADS1
    nsv343insertion1nstd2human NCBI35 chr11: 61,294,746-61,326,534 , GRCh37.p13 chr11: 61,538,170-61,569,958 , GRCh38.p12 chr11: 61,770,698-61,802,486 MYRF, TMEM258, 3 more genes
    nsv1588174short tandem repeat2nstd128human GRCh37 chr11: 61,558,732-61,558,744 , GRCh38.p12 chr11: 61,791,260-61,791,272 MIR611, FEN1, 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
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 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
    nsv3890886copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 58,935,215-62,177,656 , GRCh38.p12 chr11: 59,167,742-62,410,184 MYRF, TMEM258, 137 more genes
    nsv3915850copy number variation1nstd102humanLikely benign GRCh37 chr11: 61,177,001-61,588,631 , GRCh38 chr11: 61,409,529-61,821,159 , NCBI36 chr11: 60,933,577-61,345,207 TMEM258, RN7SL23P, 18 more genes
    nsv7093694copy number variation2nstd102humanUncertain significance GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878 VPS37C, POLR2G, 298 more genes
    nsv4675148copy number variation1nstd102humanUncertain significance GRCh37 chr11: 60,385,382-62,456,278 , GRCh38.p12 chr11: 60,617,909-62,688,806 LOC105369326, MS4A18, 91 more genes
    nsv984845copy number variation3nstd11human NCBI36 chr11: 188,510-134,449,982 , GRCh37.p13 chr11: 198,510-134,944,770 , GRCh38.p12 chr11: 198,510-135,074,876 ACAT1, ACP2, 2903 more genes
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