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Items: 1 to 20 of 234

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094847copy number variation1nstd102humanUncertain significance GRCh37 chr16: 5,132,540-5,134,882 , GRCh38.p12 chr16: 5,082,539-5,084,881 EEF2KMT, ALG1
    nsv7094836copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,293,141-5,971,108 , GRCh38.p12 chr16: 3,243,141-5,921,107 MGRN1, CORO7, 76 more genes
    nsv7076112inversion1nstd229human GRCh38 chr16: 5,090,152-5,090,823 , GRCh37.p13 chr16: 5,140,153-5,140,824 EEF2KMT
    nsv6977167copy number variation1nstd229human GRCh38 chr16: 5,074,964-5,094,285 , GRCh37.p13 chr16: 5,124,965-5,144,286 EEF2KMT, ALG1
    nsv6977161copy number variation1nstd229human GRCh38 chr16: 5,045,023-5,301,330 , GRCh37.p13 chr16: 5,095,024-5,351,331 C16orf89, LOC105371067, 8 more genes
    nsv6976824copy number variation1nstd229human GRCh38 chr16: 5,094,319-5,100,632 , GRCh37.p13 chr16: 5,144,320-5,150,633 EEF2KMT
    nsv6976189copy number variation1nstd229human GRCh38 chr16: 5,087,943-5,441,370 , GRCh37.p13 chr16: 5,137,944-5,491,371 LOC107984828, NPM1P3, 7 more genes
    nsv6974061copy number variation1nstd229human GRCh38 chr16: 4,964,551-5,150,163 , GRCh37.p13 chr16: 5,014,552-5,200,164 ENPP7P14, NAGPA, 6 more genes
    nsv6971860copy number variation1nstd229human GRCh38 chr16: 5,067,262-5,176,053 , GRCh37.p13 chr16: 5,117,263-5,226,054 ALG1, LOC107984828, 2 more genes
    nsv6971609copy number variation1nstd229human GRCh38 chr16: 5,055,134-5,134,275 , GRCh37.p13 chr16: 5,105,135-5,184,276 C16orf89, LOC107984828, 3 more genes
    nsv6971134copy number variation1nstd229human GRCh38 chr16: 4,989,753-5,161,670 , GRCh37.p13 chr16: 5,039,754-5,211,671 NAGPA, LOC107984828, 6 more genes
    nsv6971020copy number variation1nstd229human GRCh38 chr16: 5,004,687-5,310,668 , GRCh37.p13 chr16: 5,054,688-5,360,669 NAGPA, LOC107984828, 11 more genes
    nsv6966578copy number variation1nstd229human GRCh38 chr16: 4,924,814-5,845,027 , GRCh37.p13 chr16: 4,974,815-5,895,028 RPS3AP48, PPL, 16 more genes
    nsv6964343copy number variation1nstd229human GRCh38 chr16: 5,098,101-5,136,500 , GRCh37.p13 chr16: 5,148,102-5,186,501 LOC107984828, ENPP7P14, 1 more genes
    nsv6962244copy number variation1nstd229human GRCh38 chr16: 5,082,201-5,086,000 , GRCh37.p13 chr16: 5,132,202-5,136,001 ALG1, EEF2KMT
    nsv6962151copy number variation1nstd229human GRCh38 chr16: 5,081,595-5,127,371 , GRCh37.p13 chr16: 5,131,596-5,177,372 EEF2KMT, ALG1, 2 more genes
    nsv6962129copy number variation1nstd229human GRCh38 chr16: 5,083,875-5,095,923 , GRCh37.p13 chr16: 5,133,876-5,145,924 EEF2KMT, ALG1
    nsv6960419copy number variation1nstd229human GRCh38 chr16: 5,073,148-5,100,978 , GRCh37.p13 chr16: 5,123,149-5,150,979 EEF2KMT, ALG1
    nsv6960093copy number variation1nstd229human GRCh38 chr16: 5,026,806-5,260,107 , GRCh37.p13 chr16: 5,076,807-5,310,108 ALG1, RBFOX1, 8 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
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