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Items: 1 to 20 of 313

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7137196copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072 ECM1P2, LOC105378240, 482 more genes
    nsv7098818copy number variation1nstd102humanPathogenic GRCh38 chr4: 11,399,082-38,137,335 , GRCh37.p13 chr4: 11,400,706-38,138,956 LOC105374542, PPARGC1A, 232 more genes
    nsv7047237inversion1nstd229human GRCh38 chr4: 15,975,453-25,472,708 , GRCh37.p13 chr4: 15,977,076-25,474,330 LOC107986219, LOC102723675, 78 more genes
    nsv7041180inversion1nstd229human GRCh38 chr4: 18,154,007-23,460,918 , GRCh37.p13 chr4: 18,155,630-23,462,541 RPL21P46, LOC105374511, 28 more genes
    nsv7039147inversion1nstd229human GRCh38 chr4: 20,707,271-20,707,386 , GRCh37.p13 chr4: 20,708,894-20,709,009 PACRGL
    nsv7038354inversion1nstd229human GRCh38 chr4: 20,659,567-21,251,620 , GRCh37.p13 chr4: 20,661,190-21,253,243 KCNIP4, LOC105374515, 1 more genes
    nsv6737592copy number variation1nstd229human GRCh38 chr4: 20,740,501-20,744,800 , GRCh37.p13 chr4: 20,742,124-20,746,423 KCNIP4, PACRGL
    nsv6734042copy number variation1nstd229human GRCh38 chr4: 20,676,573-20,694,815 , GRCh37.p13 chr4: 20,678,196-20,696,438 PACRGL
    nsv6733885copy number variation1nstd229human GRCh38 chr4: 20,710,383-20,710,715 , GRCh37.p13 chr4: 20,712,006-20,712,338 PACRGL
    nsv6733331copy number variation1nstd229human GRCh38 chr4: 20,706,201-20,710,400 , GRCh37.p13 chr4: 20,707,824-20,712,023 PACRGL
    nsv6732953copy number variation1nstd229human GRCh38 chr4: 20,714,701-20,722,300 , GRCh37.p13 chr4: 20,716,324-20,723,923 PACRGL
    nsv6732592copy number variation1nstd229human GRCh38 chr4: 20,730,565-20,730,595 , GRCh37.p13 chr4: 20,732,188-20,732,218 KCNIP4, PACRGL
    nsv6731786copy number variation1nstd229human GRCh38 chr4: 20,725,150-20,725,499 , GRCh37.p13 chr4: 20,726,773-20,727,122 PACRGL
    nsv6729077copy number variation1nstd229human GRCh38 chr4: 20,701,413-20,702,288 , GRCh37.p13 chr4: 20,703,036-20,703,911 PACRGL
    nsv6726086copy number variation1nstd229human GRCh38 chr4: 20,737,901-21,138,600 , GRCh37.p13 chr4: 20,739,524-21,140,223 KCNIP4, PACRGL
    nsv6722058copy number variation1nstd229human GRCh38 chr4: 20,728,403-20,728,882 , GRCh37.p13 chr4: 20,730,026-20,730,505 PACRGL, KCNIP4
    nsv6718287copy number variation1nstd229human GRCh38 chr4: 20,716,501-20,721,200 , GRCh37.p13 chr4: 20,718,124-20,722,823 PACRGL
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