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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054680inversion1nstd229human GRCh38 chr3: 157,111,014-157,112,573 , GRCh37.p13 chr3: 156,828,803-156,830,362 LINC00880
    nsv7054400inversion1nstd229human GRCh38 chr3: 157,112,285-157,115,659 , GRCh37.p13 chr3: 156,830,074-156,833,448 LINC00880
    nsv7047569inversion1nstd229human GRCh38 chr3: 152,490,812-161,531,961 , GRCh37.p13 chr3: 152,208,601-161,249,749 RPS2P19, LOC112268450, 128 more genes
    nsv7039287inversion1nstd229human GRCh38 chr3: 157,123,433-157,123,574 , GRCh37.p13 chr3: 156,841,222-156,841,363 LINC00880
    nsv6734371copy number variation1nstd229human GRCh38 chr3: 156,578,264-157,290,961 , GRCh37.p13 chr3: 156,296,053-157,008,750 PA2G4P4, METTL15P1, 17 more genes
    nsv6731826copy number variation1nstd229human GRCh38 chr3: 157,089,316-157,089,518 , GRCh37.p13 chr3: 156,807,105-156,807,307 LINC00881, LINC00880
    nsv6731583copy number variation1nstd229human GRCh38 chr3: 157,111,001-157,115,700 , GRCh37.p13 chr3: 156,828,790-156,833,489 LINC00880
    nsv6731371copy number variation1nstd229human GRCh38 chr3: 157,090,986-157,092,990 , GRCh37.p13 chr3: 156,808,775-156,810,779 LINC00881, LINC00880
    nsv6730002copy number variation1nstd229human GRCh38 chr3: 157,042,514-157,119,831 , GRCh37.p13 chr3: 156,760,303-156,837,620 LINC02029, LEKR1, 2 more genes
    nsv6729239copy number variation1nstd229human GRCh38 chr3: 157,065,301-157,081,457 , GRCh37.p13 chr3: 156,783,090-156,799,246 LINC00880, LINC02029
    nsv6726957copy number variation1nstd229human GRCh38 chr3: 157,103,570-157,130,939 , GRCh37.p13 chr3: 156,821,359-156,848,728 LINC00880
    nsv6719244copy number variation1nstd229human GRCh38 chr3: 157,080,283-157,083,616 , GRCh37.p13 chr3: 156,798,072-156,801,405 LINC02029, LINC00880
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6628705copy number variation1nstd224human GRCh37 chr3: 156,570,680-156,821,808 , GRCh38.p12 chr3: 156,852,891-157,104,019 LINC00880, LEKR1, 5 more genes
    nsv6367128copy number variation1nstd223human GRCh38 chr3: 157,097,641-157,100,111 , GRCh37.p13 chr3: 156,815,430-156,817,900 LINC00880, LINC00881
    nsv6365007copy number variation1nstd223human GRCh38 chr3: 157,090,501-157,092,900 , GRCh37.p13 chr3: 156,808,290-156,810,689 LINC00880, LINC00881
    nsv6360225copy number variation1nstd223human GRCh38 chr3: 157,120,201-157,121,000 , GRCh37.p13 chr3: 156,837,990-156,838,789 LINC00880
    nsv6358733copy number variation1nstd223human GRCh38 chr3: 157,117,001-157,122,800 , GRCh37.p13 chr3: 156,834,790-156,840,589 LINC00880
    nsv6313678copy number variation1nstd102humanPathogenic GRCh37 chr3: 145,486,960-160,504,834 , GRCh38.p12 chr3: 145,769,173-160,787,046 RNU6-901P, RPL32P8, 229 more genes
    nsv6313664copy number variation1nstd102humanUncertain significance GRCh37 chr3: 156,768,935-160,158,553 , GRCh38.p12 chr3: 157,051,146-160,440,765 LOC105374179, RPL15P6, 49 more genes
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