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Items: 1 to 20 of 318

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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
    nsv7057432inversion1nstd229human GRCh38 chr4: 4,018,387-9,499,063 , GRCh37.p13 chr4: 4,020,114-9,500,707 CPZ, OR7E85P, 127 more genes
    nsv7057425inversion1nstd229human GRCh38 chr4: 3,715,710-4,814,110 , GRCh37.p13 chr4: 3,717,437-4,815,837 UNC93B4, STX18, 30 more genes
    nsv7056110inversion1nstd229human GRCh38 chr4: 3,991,106-9,653,685 , GRCh37.p13 chr4: 3,992,833-9,655,309 MAN2B2, SH3TC1, 134 more genes
    nsv7050522inversion1nstd229human GRCh38 chr4: 4,174,346-12,367,773 , GRCh37.p13 chr4: 4,176,073-12,369,397 USP17L29, MIR4274, 165 more genes
    nsv7044696inversion1nstd229human GRCh38 chr4: 3,996,444-9,648,382 , GRCh37.p13 chr4: 3,998,171-9,650,006 EVC, USP17L18, 134 more genes
    nsv7039148inversion1nstd229human GRCh38 chr4: 4,150,240-8,956,846 , GRCh37.p13 chr4: 4,151,967-8,958,572 PPP2R2C, CRMP1, 80 more genes
    nsv7038223inversion1nstd229human GRCh38 chr4: 3,989,150-9,655,696 , GRCh37.p13 chr4: 3,990,877-9,657,320 RNA5SP152, MRFAP1, 134 more genes
    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
    nsv6733296copy number variation1nstd229human GRCh38 chr4: 4,404,902-4,405,381 , GRCh37.p13 chr4: 4,406,629-4,407,108 NSG1
    nsv6725447copy number variation1nstd229human GRCh38 chr4: 3,485,667-4,651,685 , GRCh37.p13 chr4: 3,487,394-4,653,412 LOC101928217, LRPAP1, 34 more genes
    nsv6725356copy number variation1nstd229human GRCh38 chr4: 3,615,597-4,391,332 , GRCh37.p13 chr4: 3,617,324-4,393,059 ADRA2C, OR7E43P, 25 more genes
    nsv6722958copy number variation1nstd229human GRCh38 chr4: 4,411,835-4,425,967 , GRCh37.p13 chr4: 4,413,562-4,427,694 NSG1, STX18
    nsv6719505copy number variation1nstd229human GRCh38 chr4: 3,818,687-4,408,084 , GRCh37.p13 chr4: 3,820,414-4,409,811 UNC93B4, LOC107986252, 20 more genes
    nsv6718977copy number variation1nstd229human GRCh38 chr4: 4,350,317-4,416,610 , GRCh37.p13 chr4: 4,352,044-4,418,337 LOC112268462, NSG1
    nsv6718881copy number variation1nstd229human GRCh38 chr4: 3,908,216-9,748,640 , GRCh37.p13 chr4: 3,909,943-9,750,264 USP17L21, CYTL1, 143 more genes
    nsv6636582copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,346-12,369,983 , GRCh38.p12 chr4: 68,454-12,368,359 NELFA, OR7E111FP, 289 more genes
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