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Items: 1 to 20 of 390

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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
    nsv7143079copy number variation1nstd232human GRCh37.p13 chr4: 3,442,359-3,442,500 , GRCh38.p12 chr4: 3,440,632-3,440,773 HGFAC
    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
    nsv6737270copy number variation1nstd229human GRCh38 chr4: 3,445,001-3,467,900 , GRCh37.p13 chr4: 3,446,728-3,469,627 DOK7, HGFAC
    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
    nsv6735655copy number variation1nstd229human GRCh38 chr4: 3,444,168-3,448,347 , GRCh37.p13 chr4: 3,445,895-3,450,074 HGFAC
    nsv6733197copy number variation1nstd229human GRCh38 chr4: 3,446,750-3,449,497 , GRCh37.p13 chr4: 3,448,477-3,451,224 HGFAC
    nsv6725718copy number variation1nstd229human GRCh38 chr4: 3,447,258-3,451,856 , GRCh37.p13 chr4: 3,448,985-3,453,583 HGFAC
    nsv6722465copy number variation1nstd229human GRCh38 chr4: 3,386,001-3,495,600 , GRCh37.p13 chr4: 3,387,728-3,497,327 LOC105374355, HGFAC, 2 more genes
    nsv6720668copy number variation1nstd229human GRCh38 chr4: 3,434,974-3,450,055 , GRCh37.p13 chr4: 3,436,701-3,451,782 HGFAC, RGS12
    nsv6636582copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,346-12,369,983 , GRCh38.p12 chr4: 68,454-12,368,359 NELFA, OR7E111FP, 289 more genes
    nsv6636256copy number variation1nstd102humanPathogenic GRCh37 chr4: 1-12,785,001 , GRCh38.p12 chr4: 10,001-12,783,377 AFAP1-AS1, LOC389199, 294 more genes
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6366311copy number variation1nstd223human GRCh38 chr4: 3,426,615-4,165,741 , GRCh37.p13 chr4: 3,428,342-4,167,468 LOC105374358, FAM86EP, 24 more genes
    nsv6315440copy number variation1nstd102humanPathogenic GRCh37 chr4: 114,784-47,569,569 , GRCh38.p12 chr4: 114,902-47,567,552 FAM86KP, ENPP7P11, 631 more genes
    nsv6315365copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-5,579,467 , GRCh38.p12 chr4: 68,453-5,577,740 LOC107986246, FAM53A, 149 more genes
    nsv6315347copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-20,964,575 , GRCh38.p12 chr4: 68,453-20,962,952 LOC100421802, ADRA2C, 375 more genes
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