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Items: 1 to 20 of 324

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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
    nsv7054319inversion1nstd229human GRCh38 chr4: 40,437,339-43,087,585 , GRCh37.p13 chr4: 40,439,356-43,089,602 RN7SKP82, RPS7P7, 33 more genes
    nsv7052792inversion1nstd229human GRCh38 chr4: 42,386,789-42,395,898 , GRCh37.p13 chr4: 42,388,806-42,397,915 LOC105374428, SHISA3
    nsv7045674inversion1nstd229human GRCh38 chr4: 42,377,555-42,377,621 , GRCh37.p13 chr4: 42,379,572-42,379,638 LOC105374428
    nsv7040375inversion1nstd229human GRCh38 chr4: 42,334,818-42,334,837 , GRCh37.p13 chr4: 42,336,835-42,336,854 LOC105374428
    nsv6736198copy number variation1nstd229human GRCh38 chr4: 42,381,976-42,387,482 , GRCh37.p13 chr4: 42,383,993-42,389,499 LOC105374428
    nsv6735276copy number variation1nstd229human GRCh38 chr4: 42,342,324-42,347,182 , GRCh37.p13 chr4: 42,344,341-42,349,199 LOC105374428
    nsv6731802copy number variation1nstd229human GRCh38 chr4: 42,338,548-42,341,221 , GRCh37.p13 chr4: 42,340,565-42,343,238 LOC105374428
    nsv6730453copy number variation1nstd229human GRCh38 chr4: 42,370,430-42,374,965 , GRCh37.p13 chr4: 42,372,447-42,376,982 LOC105374428
    nsv6730315copy number variation1nstd229human GRCh38 chr4: 42,234,282-42,303,689 , GRCh37.p13 chr4: 42,236,299-42,305,706 LOC105374428
    nsv6726048copy number variation1nstd229human GRCh38 chr4: 42,355,322-42,361,002 , GRCh37.p13 chr4: 42,357,339-42,363,019 LOC105374428
    nsv6724443copy number variation1nstd229human GRCh38 chr4: 42,325,095-42,334,553 , GRCh37.p13 chr4: 42,327,112-42,336,570 LOC105374428
    nsv6723583copy number variation1nstd229human GRCh38 chr4: 42,369,581-42,370,346 , GRCh37.p13 chr4: 42,371,598-42,372,363 LOC105374428
    nsv6723221copy number variation1nstd229human GRCh38 chr4: 42,367,831-42,369,446 , GRCh37.p13 chr4: 42,369,848-42,371,463 LOC105374428
    nsv6721338copy number variation1nstd229human GRCh38 chr4: 42,323,208-42,391,472 , GRCh37.p13 chr4: 42,325,225-42,393,489 LOC105374428
    nsv6719022copy number variation1nstd229human GRCh38 chr4: 42,335,056-42,337,083 , GRCh37.p13 chr4: 42,337,073-42,339,100 LOC105374428
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6629868copy number variation1nstd224human GRCh37 chr4: 42,156,069-42,639,186 , GRCh38.p12 chr4: 42,154,052-42,637,169 ATP8A1, SHISA3, 3 more genes
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