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Items: 1 to 20 of 169

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095479copy number variation1nstd102humanUncertain significance GRCh37 chr19: 38,375,572-39,738,787 , GRCh38.p12 chr19: 37,884,932-39,248,147 HNRNPL, RN7SL663P, 45 more genes
    nsv7095205copy number variation2nstd102humanUncertain significance GRCh37 chr19: 39,205,089-40,913,839 , GRCh38.p12 chr19: 38,714,449-40,407,932 CCNP, NFKBIB, 81 more genes
    nsv7075514inversion1nstd229human GRCh38 chr19: 38,994,526-39,502,034 , GRCh37.p13 chr19: 39,485,166-39,992,674 RPS16, PLEKHG2, 25 more genes
    nsv7071361inversion1nstd229human GRCh38 chr19: 39,004,066-42,402,005 , GRCh37.p13 chr19: 39,494,706-42,906,157 RAB4B, RABAC1, 160 more genes
    nsv7068288inversion1nstd229human GRCh38 chr19: 39,023,970-42,945,419 , GRCh37.p13 chr19: 39,514,610-43,449,571 MIR4530, RNU6-195P, 178 more genes
    nsv7014583copy number variation1nstd229human GRCh38 chr19: 39,182,103-39,207,187 , GRCh37.p13 chr19: 39,672,743-39,697,827 PAK4, SYCN, 1 more genes
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7002869copy number variation1nstd229human GRCh38 chr19: 38,872,385-39,331,882 , GRCh37.p13 chr19: 39,363,025-39,822,522 IFNL4P1, IFNL4, 19 more genes
    nsv6531882copy number variation1nstd223human GRCh38 chr19: 38,872,385-39,331,882 , GRCh37.p13 chr19: 39,363,025-39,822,522 NFKBIB, IFNL3, 19 more genes
    nsv6530587copy number variation1nstd223human GRCh38 chr19: 39,197,689-39,199,546 , GRCh37.p13 chr19: 39,688,329-39,690,186 NCCRP1
    nsv6528813copy number variation1nstd223human GRCh38 chr19: 39,198,699-39,201,487 , GRCh37.p13 chr19: 39,689,339-39,692,127 SYCN, NCCRP1
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6226909copy number variation1nstd214human GRCh38 chr19: 39,196,751-39,196,822 , GRCh37.p13 chr19: 39,687,391-39,687,462 NCCRP1
    nsv6209455copy number variation1nstd214human GRCh38 chr19: 39,196,680-39,196,753 , GRCh37.p13 chr19: 39,687,320-39,687,393 NCCRP1
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv6105093insertion1nstd212human GRCh38 chr19: 39,196,801-39,196,801 , GRCh37.p13 chr19: 39,687,441-39,687,441 NCCRP1
    nsv6103197insertion1nstd212human GRCh38 chr19: 39,196,716-39,196,716 , GRCh37.p13 chr19: 39,687,356-39,687,356 NCCRP1
    nsv6102240insertion1nstd212human GRCh38 chr19: 39,196,760-39,196,760 , GRCh37.p13 chr19: 39,687,400-39,687,400 NCCRP1
    nsv6053970copy number variation1nstd212human GRCh38 chr19: 39,196,736-39,196,809 , GRCh37.p13 chr19: 39,687,376-39,687,449 NCCRP1
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