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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5888087copy number variation1nstd209human GRCh38 chr6: 104,015,993-104,020,752 , GRCh37.p13 chr6: 104,463,868-104,468,627 R3HDM2P2
    nsv5843877copy number variation1nstd209human GRCh38 chr6: 104,015,963-104,020,915 , GRCh37.p13 chr6: 104,463,838-104,468,790 R3HDM2P2
    nsv5472570copy number variation1nstd206human GRCh38 chr6: 104,015,993-104,020,753 , GRCh37.p13 chr6: 104,463,868-104,468,628 R3HDM2P2
    nsv5369554translocation1nstd200human GRCh38 chr6: 104,015,993-104,015,993 , GRCh38 chr6: 104,020,753-104,020,753 , GRCh37.p13 chr6: 104,463,868-104,463,868 , GRCh37.p13 chr6: 104,468,628-104,468,628 R3HDM2P2
    nsv5344445translocation1nstd200human GRCh37 chr6: 104,463,868-104,463,868 , GRCh37 chr6: 104,468,628-104,468,628 , GRCh38.p12 chr6: 104,015,993-104,015,993 , GRCh38.p12 chr6: 104,020,753-104,020,753 R3HDM2P2
    nsv5303765copy number variation1nstd204human GRCh37.p13 chr6: 104,354,223-104,885,204 , GRCh38.p13 chr6: 103,906,348-104,437,329 NPM1P10, R3HDM2P2, 2 more genes
    nsv5236730copy number variation1nstd204human GRCh38.p13 chr6: 104,014,470-104,015,737 , GRCh37.p13 chr6: 104,462,345-104,463,612 R3HDM2P2
    nsv5225819copy number variation1nstd204human GRCh38.p13 chr6: 103,906,401-104,402,600 , GRCh37.p13 chr6: 104,354,276-104,850,475 R3HDM2P2, NPM1P10, 2 more genes
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4942626copy number variation1nstd200human GRCh38 chr6: 103,968,670-104,158,448 , GRCh37.p13 chr6: 104,416,545-104,606,323 R3HDM2P2, NPM1P10
    nsv4817337copy number variation1nstd200human GRCh37 chr6: 104,354,233-104,885,195 , GRCh38.p12 chr6: 103,906,358-104,437,320 LOC105377917, NPM1P10, 2 more genes
    nsv4768376copy number variation1nstd102humanPathogenic GRCh37 chr6: 98,949,950-114,533,905 , GRCh38.p12 chr6: 98,502,074-114,212,741 LOC101927405, GPR6, 211 more genes
    nsv4685989copy number variation1nstd102humanPathogenic GRCh37 chr6: 101,287,058-117,013,245 , GRCh38.p12 chr6: 100,839,182-116,692,082 RPL23AP50, RNU6-960P, 216 more genes
    nsv4617213copy number variation1nstd183human GRCh37 chr6: 104,463,876-104,468,624 , GRCh38.p12 chr6: 104,016,001-104,020,749 R3HDM2P2
    nsv4609210copy number variation1nstd183human GRCh37 chr6: 104,324,963-104,467,061 , GRCh38.p12 chr6: 103,877,088-104,019,186 R3HDM2P2
    nsv4602723copy number variation1nstd183human GRCh37 chr6: 104,324,309-104,463,505 , GRCh38.p12 chr6: 103,876,434-104,015,630 R3HDM2P2
    nsv4570417mobile element insertion1nstd166human GRCh37.p13 chr6: 104,464,133-104,464,133 , GRCh38.p12 chr6: 104,016,258-104,016,258 R3HDM2P2
    nsv4398152copy number variation1nstd174human GRCh37 chr6: 104,462,081-104,469,545 , GRCh38.p12 chr6: 104,014,206-104,021,670 R3HDM2P2
    nsv4374080copy number variation1nstd173human GRCh37 chr6: 104,166,021-104,943,763 , GRCh38.p12 chr6: 103,718,146-104,495,888 LOC105377918, LOC102724443, 3 more genes
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
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