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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
    nsv7144519insertion1nstd232human GRCh37.p13 chr4: 3,311,990-3,311,990 , GRCh38.p12 chr4: 3,310,263-3,310,263 RGS12
    nsv7137913insertion1nstd232human GRCh37.p13 chr4: 3,295,694-3,295,694 , GRCh38.p12 chr4: 3,293,967-3,293,967 RGS12
    nsv7137271copy number variation1nstd232human GRCh37.p13 chr4: 3,414,790-3,414,892 , GRCh38.p12 chr4: 3,413,063-3,413,165 RGS12
    nsv7137196copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072 ECM1P2, LOC105378240, 482 more genes
    nsv7042908inversion1nstd229human GRCh38 chr4: 3,054,197-3,526,616 , GRCh37.p13 chr4: 3,055,924-3,528,343 HGFAC, LOC100286945, 9 more genes
    nsv6737128copy number variation1nstd229human GRCh38 chr4: 3,407,724-3,407,923 , GRCh37.p13 chr4: 3,409,451-3,409,650 RGS12
    nsv6736166copy number variation1nstd229human GRCh38 chr4: 3,268,098-4,744,559 , GRCh37.p13 chr4: 3,269,825-4,746,286 LOC105374355, LOC105374358, 40 more genes
    nsv6736052copy number variation1nstd229human GRCh38 chr4: 3,356,196-3,363,038 , GRCh37.p13 chr4: 3,357,923-3,364,765 RGS12
    nsv6735312copy number variation1nstd229human GRCh38 chr4: 3,344,407-3,344,618 , GRCh37.p13 chr4: 3,346,134-3,346,345 RGS12
    nsv6733795copy number variation1nstd229human GRCh38 chr4: 3,353,164-3,354,993 , GRCh37.p13 chr4: 3,354,891-3,356,720 RGS12
    nsv6733621copy number variation1nstd229human GRCh38 chr4: 3,382,722-3,384,280 , GRCh37.p13 chr4: 3,384,449-3,386,007 RGS12
    nsv6733290copy number variation1nstd229human GRCh38 chr4: 3,348,901-3,363,600 , GRCh37.p13 chr4: 3,350,628-3,365,327 RGS12
    nsv6732731copy number variation1nstd229human GRCh38 chr4: 3,329,651-3,329,812 , GRCh37.p13 chr4: 3,331,378-3,331,539 RGS12
    nsv6730607copy number variation1nstd229human GRCh38 chr4: 3,350,901-3,364,800 , GRCh37.p13 chr4: 3,352,628-3,366,527 RGS12
    nsv6729040copy number variation1nstd229human GRCh38 chr4: 3,351,101-3,363,700 , GRCh37.p13 chr4: 3,352,828-3,365,427 RGS12
    nsv6728729copy number variation1nstd229human GRCh38 chr4: 3,302,402-3,305,490 , GRCh37.p13 chr4: 3,304,129-3,307,217 RGS12
    nsv6728282copy number variation1nstd229human GRCh38 chr4: 3,323,365-3,333,181 , GRCh37.p13 chr4: 3,325,092-3,334,908 RPL7AP29, RGS12
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