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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143789copy number variation1nstd232human GRCh37.p13 chr19: 39,308,004-39,308,089 , GRCh38.p12 chr19: 38,817,364-38,817,449 , GRCh38.p12 chr19|NW_014040929.1: 227,036-227,121 ECH1
    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
    nsv7073355inversion1nstd229human GRCh38 chr19: 38,760,450-38,833,692 , GRCh37.p13 chr19: 39,251,090-39,324,332 LGALS7B, RNU6-140P, 3 more genes
    nsv7016233copy number variation1nstd229human GRCh38 chr19: 38,822,222-38,834,681 , GRCh37.p13 chr19: 39,312,862-39,325,321 HNRNPL, ECH1
    nsv7011890copy number variation1nstd229human GRCh38 chr19: 38,832,201-38,835,500 , GRCh37.p13 chr19: 39,322,841-39,326,140 HNRNPL, ECH1
    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
    nsv7006482copy number variation1nstd229human GRCh38 chr19: 38,816,483-38,817,076 , GRCh37.p13 chr19: 39,307,123-39,307,716 ECH1
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7002068copy number variation1nstd229human GRCh38 chr19: 38,758,871-38,818,740 , GRCh37.p13 chr19: 39,249,511-39,309,380 RNU6-140P, ECH1, 3 more genes
    nsv6998973copy number variation1nstd229human GRCh38 chr19: 38,827,604-38,827,786 , GRCh37.p13 chr19: 39,318,244-39,318,426 ECH1
    nsv6598894inversion1nstd223human GRCh38 chr19: 38,828,414-38,829,292 , GRCh37.p13 chr19: 39,319,054-39,319,932 ECH1
    nsv6598191inversion1nstd223human GRCh38 chr19: 38,828,790-38,829,101 , GRCh37.p13 chr19: 39,319,430-39,319,741 ECH1
    nsv6534932copy number variation1nstd223human GRCh38 chr19: 38,822,222-38,834,677 , GRCh37.p13 chr19: 39,312,862-39,325,317 HNRNPL, ECH1
    nsv6534792copy number variation1nstd223human GRCh38 chr19: 38,822,114-38,822,498 , GRCh37.p13 chr19: 39,312,754-39,313,138 ECH1
    nsv6526448copy number variation1nstd223human GRCh38 chr19: 38,758,834-38,818,779 , GRCh37.p13 chr19: 39,249,474-39,309,419 LGALS4, LGALS7, 3 more genes
    nsv6524029copy number variation1nstd223human GRCh38 chr19: 38,819,059-38,819,996 , GRCh37.p13 chr19: 39,309,699-39,310,636 ECH1
    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
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv6044623copy number variation1nstd212human GRCh38 chr19: 38,827,082-38,827,152 , GRCh37.p13 chr19: 39,317,722-39,317,792 ECH1
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