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Items: 1 to 20 of 235

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964552insertion1nstd209human GRCh38 chr2: 99,365,718-99,365,718 , GRCh37.p13 chr2: 99,982,181-99,982,181 EIF5B
    nsv5883570copy number variation1nstd209human GRCh38 chr2: 99,400,191-99,400,242 , GRCh37.p13 chr2: 100,016,654-100,016,705 EIF5B, REV1
    nsv5690852mobile element insertion1nstd211human GRCh38 chr2: 99,379,763-99,379,763 , GRCh37.p13 chr2: 99,996,226-99,996,226 EIF5B
    nsv5678589mobile element insertion1nstd211human GRCh38 chr2: 99,346,616-99,346,616 , GRCh37.p13 chr2: 99,963,079-99,963,079 EIF5B
    nsv5623591insertion1nstd207human GRCh38 chr2: 99,400,191-99,400,191 , GRCh37.p13 chr2: 100,016,654-100,016,654 EIF5B, REV1
    nsv5579342copy number variation1nstd207human GRCh38 chr2: 99,400,191-99,400,242 , GRCh37.p13 chr2: 100,016,654-100,016,705 EIF5B, REV1
    nsv5563478sequence alteration1nstd206human GRCh38 chr2: 99,365,717-99,365,717 , GRCh37.p13 chr2: 99,982,180-99,982,180 EIF5B
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5336792translocation1nstd200human GRCh37 chr2: 99,982,180-99,982,180 , GRCh37 chr2: 99,983,050-99,983,050 , GRCh38.p12 chr2: 99,365,717-99,365,717 , GRCh38.p12 chr2: 99,366,587-99,366,587 EIF5B
    nsv5216825copy number variation1nstd204human GRCh38.p13 chr2: 99,352,927-99,355,426 , GRCh37.p13 chr2: 99,969,390-99,971,889 EIF5B
    nsv5208224copy number variation1nstd204human GRCh38.p13 chr2: 99,337,992-99,340,293 , GRCh37.p13 chr2: 99,954,455-99,956,756 EIF5B
    nsv5192673mobile element insertion1nstd203human GRCh38 chr2: 99,368,949-99,368,963 , GRCh37.p13 chr2: 99,985,412-99,985,426 EIF5B
    nsv5068910mobile element insertion1nstd203human GRCh38 chr2: 99,352,602-99,352,651 , GRCh37.p13 chr2: 99,969,065-99,969,114 EIF5B
    nsv5060561mobile element insertion1nstd203human GRCh38 chr2: 99,353,005-99,353,032 , GRCh37.p13 chr2: 99,969,468-99,969,495 EIF5B
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4908260copy number variation1nstd200human GRCh38 chr2: 99,338,859-99,349,836 , GRCh37.p13 chr2: 99,955,322-99,966,299 EIF5B
    nsv4777167copy number variation1nstd200human GRCh37 chr2: 99,969,172-99,969,670 , GRCh38.p12 chr2: 99,352,709-99,353,207 EIF5B
    nsv4766632inversion1nstd199human GRCh37 chr2: 87,997,505-112,010,501 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,697,986-111,252,924 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 706 more genes
    nsv4755984insertion1nstd199human GRCh37 chr2: 99,982,178-99,982,178 , GRCh38.p12 chr2: 99,365,715-99,365,715 EIF5B
    nsv4752571inversion1nstd199human GRCh37 chr2: 87,550,795-112,295,517 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,323,672-111,537,940 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 723 more genes
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