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Items: 1 to 20 of 211

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7012709copy number variation1nstd229human GRCh38 chr19: 4,346,682-4,349,777 , GRCh37.p13 chr19: 4,346,679-4,349,774 MPND, EIF1P6
    nsv7012203copy number variation1nstd229human GRCh38 chr19: 4,350,958-4,365,304 , GRCh37.p13 chr19: 4,350,955-4,365,301 MPND, SH3GL1
    nsv7005968copy number variation1nstd229human GRCh38 chr19: 4,356,296-4,368,845 , GRCh37.p13 chr19: 4,356,293-4,368,842 MPND, SH3GL1
    nsv6634858copy number variation1nstd227human GRCh38.p12 chr19: 4,340,745-4,575,361 , GRCh37 chr19: 4,340,742-4,575,373 SH3GL1, CHAF1A, 10 more genes
    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
    nsv6535576copy number variation1nstd223human GRCh38 chr19: 4,349,283-4,349,718 , GRCh37.p13 chr19: 4,349,280-4,349,715 MPND, EIF1P6
    nsv6533884copy number variation1nstd223human GRCh38 chr19: 4,345,288-4,348,116 , GRCh37.p13 chr19: 4,345,285-4,348,113 EIF1P6, MPND
    nsv6530536copy number variation1nstd223human GRCh38 chr19: 4,347,415-4,348,477 , GRCh37.p13 chr19: 4,347,412-4,348,474 EIF1P6, MPND
    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
    nsv6523041copy number variation1nstd223human GRCh38 chr19: 4,348,466-4,349,683 , GRCh37.p13 chr19: 4,348,463-4,349,680 MPND, EIF1P6
    nsv6521455copy number variation1nstd223human GRCh38 chr19: 4,348,155-4,349,774 , GRCh37.p13 chr19: 4,348,152-4,349,771 MPND, EIF1P6
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