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Items: 1 to 20 of 346

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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
    nsv7048844inversion1nstd229human GRCh38 chr4: 4,924,889-4,924,952 , GRCh37.p13 chr4: 4,926,616-4,926,679 LOC101928306
    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
    nsv6737264copy number variation1nstd229human GRCh38 chr4: 4,965,947-4,966,016 , GRCh37.p13 chr4: 4,967,674-4,967,743 LOC101928306
    nsv6735689copy number variation1nstd229human GRCh38 chr4: 4,935,047-4,938,750 , GRCh37.p13 chr4: 4,936,774-4,940,477 LOC101928306
    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
    nsv6735369copy number variation1nstd229human GRCh38 chr4: 4,915,030-4,923,202 , GRCh37.p13 chr4: 4,916,757-4,924,929 RN7SKP113, LOC107986218, 1 more genes
    nsv6733592copy number variation1nstd229human GRCh38 chr4: 4,914,314-4,920,164 , GRCh37.p13 chr4: 4,916,041-4,921,891 LOC101928306, RN7SKP113, 1 more genes
    nsv6729359copy number variation1nstd229human GRCh38 chr4: 4,916,752-4,925,078 , GRCh37.p13 chr4: 4,918,479-4,926,805 LOC107986218, RN7SKP113, 1 more genes
    nsv6729276copy number variation1nstd229human GRCh38 chr4: 4,946,586-4,951,684 , GRCh37.p13 chr4: 4,948,313-4,953,411 LOC101928306
    nsv6728948copy number variation1nstd229human GRCh38 chr4: 4,979,561-4,988,233 , GRCh37.p13 chr4: 4,981,288-4,989,960 LOC101928306
    nsv6728731copy number variation1nstd229human GRCh38 chr4: 4,483,158-4,982,254 , GRCh37.p13 chr4: 4,484,885-4,983,981 LINC03091, LOC101928306, 11 more genes
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