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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7053565inversion1nstd229human GRCh38 chr4: 2,195,256-2,195,294 , GRCh37.p13 chr4: 2,196,983-2,197,021 POLN
    nsv7049879inversion1nstd229human GRCh38 chr4: 2,192,166-2,195,993 , GRCh37.p13 chr4: 2,193,893-2,197,720 POLN
    nsv7049289inversion1nstd229human GRCh38 chr4: 1,879,237-2,966,412 , GRCh37.p13 chr4: 1,880,964-2,968,139 RNF4, SCARNA22, 28 more genes
    nsv7045507inversion1nstd229human GRCh38 chr4: 2,153,682-2,154,199 , GRCh37.p13 chr4: 2,155,409-2,155,926 POLN
    nsv7044843inversion1nstd229human GRCh38 chr4: 2,164,081-2,167,461 , GRCh37.p13 chr4: 2,165,808-2,169,188 POLN
    nsv7041631inversion1nstd229human GRCh38 chr4: 2,160,823-2,167,657 , GRCh37.p13 chr4: 2,162,550-2,169,384 POLN
    nsv7039441inversion1nstd229human GRCh38 chr4: 1,689,472-2,959,448 , GRCh37.p13 chr4: 1,691,199-2,961,175 NOP14-AS1, LOC112268460, 34 more genes
    nsv6736923copy number variation1nstd229human GRCh38 chr4: 2,160,969-2,164,080 , GRCh37.p13 chr4: 2,162,696-2,165,807 POLN
    nsv6734537copy number variation1nstd229human GRCh38 chr4: 2,195,123-2,201,783 , GRCh37.p13 chr4: 2,196,850-2,203,510 POLN
    nsv6730394copy number variation1nstd229human GRCh38 chr4: 2,200,486-2,609,402 , GRCh37.p13 chr4: 2,202,213-2,611,129 MIR4800, LOC105374352, 13 more genes
    nsv6729949copy number variation1nstd229human GRCh38 chr4: 2,167,550-2,173,218 , GRCh37.p13 chr4: 2,169,277-2,174,945 POLN
    nsv6728594copy number variation1nstd229human GRCh38 chr4: 2,200,502-2,212,519 , GRCh37.p13 chr4: 2,202,229-2,214,246 POLN
    nsv6728163copy number variation1nstd229human GRCh38 chr4: 2,164,288-2,171,340 , GRCh37.p13 chr4: 2,166,015-2,173,067 POLN
    nsv6726871copy number variation1nstd229human GRCh38 chr4: 2,234,148-2,235,473 , GRCh37.p13 chr4: 2,235,875-2,237,200 COX6B1P5, HAUS3, 1 more genes
    nsv6726652copy number variation1nstd229human GRCh38 chr4: 2,067,576-2,071,110 , GRCh37.p13 chr4: 2,069,303-2,072,837 POLN, NAT8L
    nsv6726433copy number variation1nstd229human GRCh38 chr4: 2,182,801-2,185,900 , GRCh37.p13 chr4: 2,184,528-2,187,627 POLN
    nsv6725535copy number variation1nstd229human GRCh38 chr4: 2,201,001-2,480,600 , GRCh37.p13 chr4: 2,202,728-2,482,327 POLN, RNF4, 12 more genes
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