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Items: 1 to 20 of 234

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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
    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
    nsv6737190copy number variation1nstd229human GRCh38 chr4: 5,524,132-5,524,159 , GRCh37.p13 chr4: 5,525,859-5,525,886 LINC01587
    nsv6736122copy number variation1nstd229human GRCh38 chr4: 5,410,363-5,631,092 , GRCh37.p13 chr4: 5,412,090-5,632,819 EVC2, LINC01587, 2 more genes
    nsv6731928copy number variation1nstd229human GRCh38 chr4: 5,385,798-5,741,452 , GRCh37.p13 chr4: 5,387,525-5,743,179 LINC01587, RN7SKP275, 3 more genes
    nsv6731623copy number variation1nstd229human GRCh38 chr4: 5,518,164-5,525,690 , GRCh37.p13 chr4: 5,519,891-5,527,417 LINC01587
    nsv6731366copy number variation1nstd229human GRCh38 chr4: 5,526,767-5,530,719 , GRCh37.p13 chr4: 5,528,494-5,532,446 LINC01587
    nsv6731249copy number variation1nstd229human GRCh38 chr4: 5,331,845-5,557,699 , GRCh37.p13 chr4: 5,333,572-5,559,426 RN7SKP275, LINC01587, 1 more genes
    nsv6729836copy number variation1nstd229human GRCh38 chr4: 5,502,601-5,586,900 , GRCh37.p13 chr4: 5,504,328-5,588,627 LINC01587, EVC2
    nsv6723208copy number variation1nstd229human GRCh38 chr4: 5,355,032-14,502,279 , GRCh37.p13 chr4: 5,356,759-14,503,903 OR7E86P, LINC02447, 164 more genes
    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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