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Items: 1 to 20 of 937

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057068inversion1nstd229human GRCh38 chr5: 116,291,335-116,291,991 , GRCh37.p13 chr5: 115,627,032-115,627,688 COMMD10
    nsv7054819inversion1nstd229human GRCh38 chr5: 112,393,108-116,183,657 , GRCh37.p13 chr5: 111,728,805-115,519,354 SRP19, LINCADL, 53 more genes
    nsv7053776inversion1nstd229human GRCh38 chr5: 115,805,593-116,116,811 , GRCh37.p13 chr5: 115,141,290-115,452,508 CDO1, ATG12, 7 more genes
    nsv7049327inversion1nstd229human GRCh38 chr5: 115,595,517-116,496,585 , GRCh37.p13 chr5: 114,931,214-115,832,281 MIR12130, COMMD10, 20 more genes
    nsv7045139inversion1nstd229human GRCh38 chr5: 116,214,870-117,260,108 , GRCh37.p13 chr5: 115,550,567-116,595,804 LOC101927190, SEMA6A-AS1, 14 more genes
    nsv7040741inversion1nstd229human GRCh38 chr5: 116,204,259-116,264,417 , GRCh37.p13 chr5: 115,539,956-115,600,114 MIR12130, HMGN2P27, 1 more genes
    nsv6778025copy number variation1nstd229human GRCh38 chr5: 116,044,920-116,190,403 , GRCh37.p13 chr5: 115,380,617-115,526,100 ARL14EPL, RNU6-644P, 2 more genes
    nsv6777552copy number variation1nstd229human GRCh38 chr5: 115,897,085-116,298,436 , GRCh37.p13 chr5: 115,232,782-115,634,133 MIR12130, COMMD10, 8 more genes
    nsv6777375copy number variation1nstd229human GRCh38 chr5: 116,105,867-116,107,932 , GRCh37.p13 chr5: 115,441,564-115,443,629 COMMD10
    nsv6777007copy number variation1nstd229human GRCh38 chr5: 116,207,156-116,210,161 , GRCh37.p13 chr5: 115,542,853-115,545,858 COMMD10
    nsv6776661copy number variation1nstd229human GRCh38 chr5: 116,104,482-116,113,151 , GRCh37.p13 chr5: 115,440,179-115,448,848 COMMD10
    nsv6776644copy number variation1nstd229human GRCh38 chr5: 116,282,713-116,361,188 , GRCh37.p13 chr5: 115,618,410-115,696,885 COMMD10
    nsv6776511copy number variation1nstd229human GRCh38 chr5: 116,103,201-116,108,300 , GRCh37.p13 chr5: 115,438,898-115,443,997 COMMD10
    nsv6776439copy number variation1nstd229human GRCh38 chr5: 116,241,870-116,380,356 , GRCh37.p13 chr5: 115,577,567-115,716,053 LOC101927190, COMMD10, 1 more genes
    nsv6776287copy number variation1nstd229human GRCh38 chr5: 116,186,301-116,194,100 , GRCh37.p13 chr5: 115,521,998-115,529,797 RNU6-644P, COMMD10
    nsv6775973copy number variation1nstd229human GRCh38 chr5: 116,085,274-116,288,679 , GRCh37.p13 chr5: 115,420,971-115,624,376 COMMD10, MIR12130, 2 more genes
    nsv6775939copy number variation1nstd229human GRCh38 chr5: 116,245,745-116,259,919 , GRCh37.p13 chr5: 115,581,442-115,595,616 MIR12130, COMMD10
    nsv6775712copy number variation1nstd229human GRCh38 chr5: 116,223,204-116,226,169 , GRCh37.p13 chr5: 115,558,901-115,561,866 COMMD10
    nsv6775355copy number variation1nstd229human GRCh38 chr5: 116,248,201-116,295,100 , GRCh37.p13 chr5: 115,583,898-115,630,797 COMMD10, MIR12130
    nsv6775245copy number variation1nstd229human GRCh38 chr5: 116,030,101-116,262,500 , GRCh37.p13 chr5: 115,365,798-115,598,197 COMMD10, RNU6-644P, 4 more genes
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