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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968084insertion1nstd209human GRCh38 chr11: 4,447,727-4,447,727 , GRCh37.p13 chr11: 4,468,957-4,468,957 OR52K2
    nsv5907651copy number variation1nstd209human GRCh38 chr11: 4,411,179-4,454,725 , GRCh37.p13 chr11: 4,432,409-4,475,955 OR51R1P, OR52K2, 1 more genes
    nsv5856169copy number variation1nstd209human GRCh38 chr11: 4,445,787-4,454,439 , GRCh37.p13 chr11: 4,467,017-4,475,669 OR52K2
    nsv5556652sequence alteration1nstd206human GRCh38 chr11: 4,438,099-4,461,909 , GRCh37.p13 chr11: 4,459,329-4,483,139 OR52K2
    nsv5507349copy number variation1nstd206human GRCh38 chr11: 4,332,000-4,540,000 , GRCh37.p13 chr11: 4,353,230-4,561,230 OR52K1, OR52P2P, 8 more genes
    nsv5248690copy number variation1nstd204human GRCh38.p13 chr11: 4,439,571-4,455,639 , GRCh37.p13 chr11: 4,460,801-4,476,869 OR52K2
    nsv5243714copy number variation1nstd204human GRCh38.p13 chr11: 4,217,901-4,523,400 , GRCh37.p13 chr11: 4,239,131-4,544,630 OR52K2, OR52M2P, 13 more genes
    nsv4977953copy number variation1nstd200human GRCh38 chr11: 4,449,871-4,656,651 , GRCh37.p13 chr11: 4,471,101-4,677,881 OR52M1, OR52K1, 9 more genes
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 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
    nsv4729112copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-4,851,537 , GRCh38.p12 chr11: 230,615-4,830,307 OR51E1, TNNI2, 203 more genes
    nsv4728922copy number variation1nstd102humanUncertain significance GRCh37 chr11: 4,388,904-4,639,840 , GRCh38.p12 chr11: 4,367,674-4,618,610 OR52K1, OR52B4, 12 more genes
    nsv4679088copy number variation1nstd189human GRCh37.p13 chr11: 4,335,879-4,833,224 , GRCh38.p12 chr11: 4,314,649-4,811,994 TRIM21, TRIM68, 29 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4606402copy number variation1nstd183human GRCh37 chr11: 4,441,838-4,476,179 , GRCh38.p12 chr11: 4,420,608-4,454,949 OR52K2, OR52P2P
    nsv4603424copy number variation2nstd183human GRCh37 chr11: 4,306,599-4,596,790 , GRCh38.p12 chr11: 4,285,369-4,575,560 OR52B4, OR52M1, 12 more genes
    nsv4428085copy number variation1nstd174human GRCh37 chr11: 4,430,146-4,489,029 , GRCh38.p12 chr11: 4,408,916-4,467,799 OR52K2, OR51R1P, 1 more genes
    nsv4423400copy number variation1nstd174human GRCh37 chr11: 4,387,484-4,589,780 , GRCh38.p12 chr11: 4,366,254-4,568,550 OR52K2, OR52M2P, 8 more genes
    nsv4381756copy number variation1nstd173human GRCh37 chr11: 4,167,416-5,153,276 , GRCh38.p12 chr11: 4,146,186-5,132,046 C11orf40, OR51H1, 62 more genes
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