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Items: 1 to 20 of 157

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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
    nsv7073355inversion1nstd229human GRCh38 chr19: 38,760,450-38,833,692 , GRCh37.p13 chr19: 39,251,090-39,324,332 LGALS7B, RNU6-140P, 3 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
    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
    nsv6599434inversion1nstd223human GRCh38 chr19: 38,769,860-38,792,818 , GRCh37.p13 chr19: 39,260,500-39,283,458 LGALS7, LGALS7B
    nsv6596717inversion1nstd223human GRCh38 chr19: 38,769,465-38,793,260 , GRCh37.p13 chr19: 39,260,105-39,283,900 LGALS7, LGALS7B
    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
    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
    nsv6144529copy number variation1nstd206human GRCh38 chr19: 38,764,399-38,791,874 , GRCh37.p13 chr19: 39,255,039-39,282,514 LGALS7, LGALS7B
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv5665548inversion1nstd207human GRCh38 chr19: 38,770,127-38,792,391 , GRCh37.p13 chr19: 39,260,767-39,283,031 LGALS7, LGALS7B
    nsv5375429translocation1nstd200human GRCh38 chr19: 38,792,816-38,792,816 , GRCh38 chr19: 38,769,795-38,769,795 , GRCh37.p13 chr19: 39,283,456-39,283,456 , GRCh37.p13 chr19: 39,260,435-39,260,435 LGALS7
    nsv5375428translocation1nstd200human GRCh38 chr19: 38,769,702-38,769,702 , GRCh38 chr19: 38,793,122-38,793,122 , GRCh37.p13 chr19: 39,260,342-39,260,342 , GRCh37.p13 chr19: 39,283,762-39,283,762 LGALS7
    nsv5332424translocation1nstd200human GRCh37 chr19: 39,283,456-39,283,456 , GRCh37 chr19: 39,260,450-39,260,450 , GRCh38.p12 chr19|NW_014040929.1: 202,498-202,498 , GRCh38.p12 chr19: 38,769,810-38,769,810 , GRCh38.p12 chr19: 38,792,816-38,792,816 , GRCh38.p12 chr19|NW_014040929.1: 179,450-179,450 LGALS7
    nsv5298555copy number variation1nstd204human GRCh38.p13 chr19: 38,771,901-38,772,500 , GRCh37.p13 chr19: 39,262,541-39,263,140 LGALS7
    nsv5024622copy number variation1nstd200human GRCh38 chr19: 38,758,799-38,818,817 , GRCh37.p13 chr19: 39,249,439-39,309,457 LGALS7, LGALS4, 3 more genes
    nsv5024620copy number variation1nstd200human GRCh38 chr19: 38,737,176-38,789,205 , GRCh37.p13 chr19: 39,227,816-39,279,845 LGALS7B, LGALS7, 1 more genes
    nsv4865159copy number variation1nstd200human GRCh37 chr19: 39,249,439-39,309,457 , GRCh38.p12 chr19|NW_014040929.1: 168,408-228,489 , GRCh38.p12 chr19: 38,758,799-38,818,817 ECH1, RNU6-140P, 3 more genes
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