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Items: 1 to 20 of 214

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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
    nsv7072026inversion1nstd229human GRCh38 chr19: 4,297,095-4,299,985 , GRCh37.p13 chr19: 4,297,092-4,299,982 TMIGD2
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 more genes
    nsv7060403inversion1nstd229human GRCh38 chr19: 4,292,193-4,314,039 , GRCh37.p13 chr19: 4,292,190-4,314,036 FSD1, TMIGD2
    nsv7060352inversion1nstd229human GRCh38 chr19: 3,851,263-4,364,229 , GRCh37.p13 chr19: 3,851,261-4,364,226 DAPK3, YJU2, 22 more genes
    nsv7013667copy number variation1nstd229human GRCh38 chr19: 4,297,630-4,300,120 , GRCh37.p13 chr19: 4,297,627-4,300,117 TMIGD2
    nsv7011097copy number variation1nstd229human GRCh38 chr19: 4,282,112-4,295,269 , GRCh37.p13 chr19: 4,282,109-4,295,266 TMIGD2, SHD
    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
    nsv6534565copy number variation1nstd223human GRCh38 chr19: 4,295,154-4,300,245 , GRCh37.p13 chr19: 4,295,151-4,300,242 TMIGD2
    nsv6531875copy number variation1nstd223human GRCh38 chr19: 4,285,926-4,297,404 , GRCh37.p13 chr19: 4,285,923-4,297,401 SHD, TMIGD2
    nsv6531291copy number variation1nstd223human GRCh38 chr19: 4,291,945-4,293,463 , GRCh37.p13 chr19: 4,291,942-4,293,460 TMIGD2
    nsv6528575copy number variation1nstd223human GRCh38 chr19: 4,291,626-4,293,415 , GRCh37.p13 chr19: 4,291,623-4,293,412 TMIGD2
    nsv6526498copy number variation1nstd223human GRCh38 chr19: 4,300,223-4,300,654 , GRCh37.p13 chr19: 4,300,220-4,300,651 TMIGD2
    nsv6523138copy number variation1nstd223human GRCh38 chr19: 4,293,175-4,293,474 , GRCh37.p13 chr19: 4,293,172-4,293,471 TMIGD2
    nsv6519593copy number variation1nstd223human GRCh38 chr19: 4,294,014-4,296,171 , GRCh37.p13 chr19: 4,294,011-4,296,168 TMIGD2
    nsv6518412copy number variation1nstd223human GRCh38 chr19: 4,287,071-4,290,855 , GRCh37.p13 chr19: 4,287,068-4,290,852 SHD, TMIGD2
    nsv6517267copy number variation1nstd223human GRCh38 chr19: 4,297,594-4,300,133 , GRCh37.p13 chr19: 4,297,591-4,300,130 TMIGD2
    nsv6515960copy number variation1nstd223human GRCh38 chr19: 4,285,846-4,293,163 , GRCh37.p13 chr19: 4,285,843-4,293,160 SHD, TMIGD2
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