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Items: 1 to 20 of 67

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5916680copy number variation1nstd209human GRCh38 chr11: 59,319,012-59,385,198 , GRCh37.p13 chr11: 59,086,485-59,152,671 OR5BR1P, OR5AN1
    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
    nsv5326104inversion1nstd204human GRCh37.p13 chr11: 58,446,123-60,252,987 , GRCh38.p13 chr11: 58,678,650-60,485,514 OSBP, OR5BB1P, 78 more genes
    nsv5325627inversion1nstd204human GRCh37.p13 chr11: 58,669,453-61,321,541 , GRCh38.p13 chr11: 58,901,980-61,554,069 , CD5, 118 more genes
    nsv4984973copy number variation1nstd200human GRCh38 chr11: 58,629,506-59,462,358 , GRCh37.p13 chr11: 58,396,979-59,229,831 GLYATL1P4, LOC283194, 29 more genes
    nsv4885672inversion1nstd200human GRCh37 chr11: 58,669,461-61,321,541 , GRCh38.p12 chr11: 58,901,988-61,554,069 , MS4A2, 118 more genes
    nsv4870911inversion1nstd200human GRCh37 chr11: 58,446,132-60,252,987 , GRCh38.p12 chr11: 58,678,659-60,485,514 LOC100422398, LOC100287485, 78 more genes
    nsv4829712copy number variation1nstd200human GRCh37 chr11: 59,101,250-59,151,326 , GRCh38.p12 chr11: 59,333,777-59,383,853 OR5BR1P, OR5AN1
    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
    nsv4568680mobile element insertion1nstd166human GRCh37.p13 chr11: 59,133,063-59,133,063 , GRCh38.p12 chr11: 59,365,590-59,365,590 OR5AN1
    nsv4561310mobile element insertion1nstd166human GRCh37.p13 chr11: 59,131,674-59,131,674 , GRCh38.p12 chr11: 59,364,201-59,364,201 OR5AN1
    nsv4387140copy number variation1nstd173human GRCh37 chr11: 59,027,897-59,315,316 , GRCh38.p12 chr11: 59,260,424-59,547,843 OR5AN1, OR4D8P, 14 more genes
    nsv4385663copy number variation1nstd173human GRCh37 chr11: 59,027,897-59,310,144 , GRCh38.p12 chr11: 59,260,424-59,542,671 OR5AN1, OR4D8P, 14 more genes
    nsv4369217copy number variation2nstd173human GRCh37 chr11: 59,127,460-59,227,430 , GRCh38.p12 chr11: 59,359,987-59,459,957 OR5A1, OR5A2, 3 more genes
    nsv4368659copy number variation1nstd173human GRCh37 chr11: 59,039,527-59,315,755 , GRCh38.p12 chr11: 59,272,054-59,548,282 OR4D10, OR5BB1P, 13 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
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 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
    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
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