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Items: 1 to 20 of 610

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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
    nsv7097002copy number variation1nstd102humanPathogenic GRCh37 chr4: 5,710,003-5,750,043 , GRCh38.p12 chr4: 5,708,276-5,748,316 EVC, EVC2
    nsv7097001copy number variation1nstd102humanPathogenic GRCh37 chr4: 5,690,874-5,696,238 , GRCh38.p12 chr4: 5,689,147-5,694,511 EVC2
    nsv7096863copy number variation1nstd102humanPathogenic GRCh37 chr4: 5,617,139-5,812,774 , GRCh38.p12 chr4: 5,615,412-5,811,047 EVC2, EVC
    nsv7096737copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 5,630,335-5,635,926 , GRCh38.p12 chr4: 5,628,608-5,634,199 EVC2
    nsv7096736copy number variation1nstd102humanPathogenic GRCh37 chr4: 5,576,402-5,576,509 , GRCh38.p12 chr4: 5,574,675-5,574,782 EVC2
    nsv7096735copy number variation1nstd102humanPathogenic GRCh37 chr4: 5,564,565-5,578,191 , GRCh38.p12 chr4: 5,562,838-5,576,464 EVC2
    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
    nsv7052322inversion1nstd229human GRCh38 chr4: 5,688,513-5,696,739 , GRCh37.p13 chr4: 5,690,240-5,698,466 EVC2
    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
    nsv7038608inversion1nstd229human GRCh38 chr4: 5,707,069-5,707,173 , GRCh37.p13 chr4: 5,708,796-5,708,900 EVC2
    nsv7038223inversion1nstd229human GRCh38 chr4: 3,989,150-9,655,696 , GRCh37.p13 chr4: 3,990,877-9,657,320 RNA5SP152, MRFAP1, 134 more genes
    nsv6737780copy number variation1nstd229human GRCh38 chr4: 5,640,171-5,640,450 , GRCh37.p13 chr4: 5,641,898-5,642,177 EVC2
    nsv6737678copy number variation1nstd229human GRCh38 chr4: 5,601,610-5,606,573 , GRCh37.p13 chr4: 5,603,337-5,608,300 EVC2
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