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Items: 1 to 20 of 596

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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
    nsv7145445insertion1nstd232human GRCh37.p13 chr4: 37,534,567-37,534,567 , GRCh38.p12 chr4: 37,532,945-37,532,945 C4orf19
    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
    nsv7055164inversion1nstd229human GRCh38 chr4: 37,533,941-37,536,673 , GRCh37.p13 chr4: 37,535,563-37,538,295 C4orf19
    nsv7052586inversion1nstd229human GRCh38 chr4: 37,564,011-37,569,041 , GRCh37.p13 chr4: 37,565,633-37,570,663 C4orf19
    nsv7046474inversion1nstd229human GRCh38 chr4: 37,567,797-37,567,893 , GRCh37.p13 chr4: 37,569,419-37,569,515 C4orf19
    nsv7043551inversion1nstd229human GRCh38 chr4: 37,476,845-37,476,870 , GRCh37.p13 chr4: 37,478,467-37,478,492 C4orf19
    nsv7042059inversion1nstd229human GRCh38 chr4: 37,555,259-37,555,289 , GRCh37.p13 chr4: 37,556,881-37,556,911 C4orf19
    nsv7039952inversion1nstd229human GRCh38 chr4: 37,593,247-37,593,265 , GRCh37.p13 chr4: 37,594,869-37,594,887 C4orf19, RELL1
    nsv6738040copy number variation1nstd229human GRCh38 chr4: 37,526,901-37,652,300 , GRCh37.p13 chr4: 37,528,523-37,653,922 RELL1, C4orf19
    nsv6736718copy number variation1nstd229human GRCh38 chr4: 37,582,222-37,587,589 , GRCh37.p13 chr4: 37,583,844-37,589,211 C4orf19
    nsv6735032copy number variation1nstd229human GRCh38 chr4: 37,547,601-37,557,400 , GRCh37.p13 chr4: 37,549,223-37,559,022 C4orf19
    nsv6734996copy number variation1nstd229human GRCh38 chr4: 37,591,217-37,594,744 , GRCh37.p13 chr4: 37,592,839-37,596,366 RELL1, C4orf19
    nsv6733650copy number variation1nstd229human GRCh38 chr4: 37,457,801-37,468,800 , GRCh37.p13 chr4: 37,459,423-37,470,422 C4orf19
    nsv6730551copy number variation1nstd229human GRCh38 chr4: 37,555,365-37,555,536 , GRCh37.p13 chr4: 37,556,987-37,557,158 C4orf19
    nsv6730169copy number variation1nstd229human GRCh38 chr4: 37,536,333-37,540,619 , GRCh37.p13 chr4: 37,537,955-37,542,241 C4orf19
    nsv6728490copy number variation1nstd229human GRCh38 chr4: 37,447,916-37,459,213 , GRCh37.p13 chr4: 37,449,538-37,460,835 C4orf19, NWD2
    nsv6727581copy number variation1nstd229human GRCh38 chr4: 28,550,139-38,411,880 , GRCh37.p13 chr4: 28,551,761-38,413,501 LINC02497, MESTP3, 66 more genes
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