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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967660inversion1nstd209human GRCh38 chr2: 97,579,662-98,035,557 , GRCh37.p13 chr2: 98,196,125-98,652,020 , COX5B, 10 more genes
    nsv5877439copy number variation1nstd209human GRCh38 chr2: 97,717,353-97,717,468 , GRCh37.p13 chr2: 98,333,816-98,333,931 ZAP70
    nsv5620222insertion1nstd207human GRCh38 chr2: 97,717,329-97,717,329 , GRCh37.p13 chr2: 98,333,792-98,333,792 ZAP70
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5297784copy number variation1nstd204human GRCh38.p13 chr2: 97,708,857-97,710,238 , GRCh37.p13 chr2: 98,325,320-98,326,701 ZAP70
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4908216copy number variation1nstd200human GRCh38 chr2: 97,712,991-97,713,093 , GRCh37.p13 chr2: 98,329,454-98,329,556 ZAP70
    nsv4908215copy number variation1nstd200human GRCh38 chr2: 97,708,880-97,710,217 , GRCh37.p13 chr2: 98,325,343-98,326,680 ZAP70
    nsv4894836copy number variation1nstd200human GRCh38 chr2: 97,717,329-97,717,523 , GRCh37.p13 chr2: 98,333,792-98,333,986 ZAP70
    nsv4777128copy number variation1nstd200human GRCh37 chr2: 98,325,343-98,326,680 , GRCh38.p12 chr2: 97,708,880-97,710,217 ZAP70
    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
    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
    nsv4751593insertion1nstd199human GRCh37 chr2: 98,333,820-98,333,820 , GRCh38.p12 chr2: 97,717,357-97,717,357 ZAP70
    nsv4743379copy number variation1nstd199human GRCh37 chr2: 88,481,090-124,440,189 , GRCh38.p12 chr9: 40,649,751-63,450,622 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 88,181,571-123,682,613 , EIF2AK3, 861 more genes
    nsv4681232copy number variation1nstd102humanUncertain significance GRCh37 chr2: 98,353,916-98,355,981 , GRCh38.p12 chr2: 97,737,453-97,739,518 ZAP70
    nsv4312591inversion1nstd166human GRCh37.p13 chr2: 97,201,014-102,197,203 , GRCh38.p12 chr2: 96,535,277-101,580,741 , CNGA3, 106 more genes
    nsv4069713copy number variation1nstd166human GRCh37.p13 chr2: 98,325,343-98,326,680 , GRCh38.p12 chr2: 97,708,880-97,710,217 ZAP70
    nsv4066674copy number variation1nstd166human GRCh37.p13 chr2: 98,334,449-98,335,527 , GRCh38.p12 chr2: 97,717,986-97,719,064 ZAP70
    nsv4060115copy number variation1nstd166human GRCh37.p13 chr2: 98,324,264-98,328,383 , GRCh38.p12 chr2: 97,707,801-97,711,920 ZAP70
    nsv4059032copy number variation1nstd166human GRCh37.p13 chr2: 98,329,454-98,329,556 , GRCh38.p12 chr2: 97,712,991-97,713,093 ZAP70
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