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Items: 1 to 20 of 275

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140442insertion1nstd232human GRCh37.p13 chr19: 4,334,813-4,334,813 , GRCh38.p12 chr19: 4,334,816-4,334,816 STAP2
    nsv7138795copy number variation1nstd232human GRCh37.p13 chr19: 4,328,415-4,328,478 , GRCh38.p12 chr19: 4,328,418-4,328,481 STAP2
    nsv7095297copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777 NCLN, RN7SL202P, 223 more genes
    nsv7095226copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-4,818,389 , GRCh38.p12 chr19: 589,946-4,818,377 ATP5F1D, LOC102723798, 204 more genes
    nsv7068649inversion1nstd229human GRCh38 chr19: 4,313,135-7,007,201 , GRCh37.p13 chr19: 4,313,132-7,007,212 CAPS, SH2D3A, 93 more genes
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 more genes
    nsv7060352inversion1nstd229human GRCh38 chr19: 3,851,263-4,364,229 , GRCh37.p13 chr19: 3,851,261-4,364,226 DAPK3, YJU2, 22 more genes
    nsv7017810copy number variation1nstd229human GRCh38 chr19: 4,323,001-4,523,900 , GRCh37.p13 chr19: 4,322,998-4,523,912 CHAF1A, FSD1, 9 more genes
    nsv7017043copy number variation1nstd229human GRCh38 chr19: 4,322,358-4,327,147 , GRCh37.p13 chr19: 4,322,355-4,327,144 FSD1, STAP2
    nsv7014130copy number variation1nstd229human GRCh38 chr19: 4,321,522-4,322,590 , GRCh37.p13 chr19: 4,321,519-4,322,587 FSD1, STAP2
    nsv7013155copy number variation1nstd229human GRCh38 chr19: 4,325,735-4,331,698 , GRCh37.p13 chr19: 4,325,732-4,331,695 STAP2
    nsv7012009copy number variation1nstd229human GRCh38 chr19: 4,325,383-4,327,283 , GRCh37.p13 chr19: 4,325,380-4,327,280 STAP2
    nsv7008827copy number variation1nstd229human GRCh38 chr19: 4,328,418-4,328,482 , GRCh37.p13 chr19: 4,328,415-4,328,479 STAP2
    nsv6624976copy number variation1nstd224human GRCh37 chr19: 4,323,195-4,375,162 , GRCh38.p12 chr19: 4,323,198-4,375,165 STAP2, MPND, 3 more genes
    nsv6598603inversion1nstd223human GRCh38 chr19: 4,262,367-4,610,905 , GRCh37.p13 chr19: 4,262,364-4,610,917 STAP2, FSD1, 15 more genes
    nsv6597296inversion1nstd223human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , ALKBH7, 192 more genes
    nsv6534671copy number variation1nstd223human GRCh38 chr19: 4,334,809-4,335,103 , GRCh37.p13 chr19: 4,334,806-4,335,100 STAP2
    nsv6533177copy number variation1nstd223human GRCh38 chr19: 4,325,734-4,331,650 , GRCh37.p13 chr19: 4,325,731-4,331,647 STAP2
    nsv6528576copy number variation1nstd223human GRCh38 chr19: 4,331,888-4,342,037 , GRCh37.p13 chr19: 4,331,885-4,342,034 MPND, STAP2
    nsv6527220copy number variation1nstd223human GRCh38 chr19: 4,320,080-4,388,602 , GRCh37.p13 chr19: 4,320,077-4,388,599 STAP2, SH3GL1, 3 more genes
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