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Items: 1 to 20 of 262

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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
    nsv7052285inversion1nstd229human GRCh38 chr4: 5,012,616-5,012,651 , GRCh37.p13 chr4: 5,014,343-5,014,378 CYTL1
    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
    nsv6735508copy number variation1nstd229human GRCh38 chr4: 4,783,311-5,226,255 , GRCh37.p13 chr4: 4,785,038-5,227,982 LDHAP1, LOC101928306, 8 more genes
    nsv6731435copy number variation1nstd229human GRCh38 chr4: 5,015,413-5,021,018 , GRCh37.p13 chr4: 5,017,140-5,022,745 CYTL1
    nsv6729496copy number variation1nstd229human GRCh38 chr4: 5,016,608-5,016,758 , GRCh37.p13 chr4: 5,018,335-5,018,485 CYTL1
    nsv6726851copy number variation1nstd229human GRCh38 chr4: 5,017,515-5,017,618 , GRCh37.p13 chr4: 5,019,242-5,019,345 CYTL1
    nsv6725759copy number variation1nstd229human GRCh38 chr4: 4,918,972-5,083,515 , GRCh37.p13 chr4: 4,920,699-5,085,242 STK32B, LOC107986218, 4 more genes
    nsv6724310copy number variation1nstd229human GRCh38 chr4: 4,911,365-5,017,052 , GRCh37.p13 chr4: 4,913,092-5,018,779 LOC101928306, CYTL1, 2 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
    nsv6636683copy number variation1nstd102humanUncertain significance GRCh37 chr4: 4,955,520-5,440,181 , GRCh38.p12 chr4: 4,953,793-5,438,454 STK32B, LOC107986256, 2 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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