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Items: 1 to 20 of 292

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137115copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,467,726-29,044,717 , GRCh38.p12 chr16: 21,456,405-29,033,396 OTOAP1, GGA2, 148 more genes
    nsv7069781inversion1nstd229human GRCh38 chr16: 24,962,563-25,492,782 , GRCh37.p13 chr16: 24,973,884-25,504,103 CYCSP39, ARHGAP17, 13 more genes
    nsv7066307inversion1nstd229human GRCh38 chr16: 25,128,995-25,267,847 , GRCh37.p13 chr16: 25,140,316-25,279,168 AQP8, LCMT1, 3 more genes
    nsv7063724inversion1nstd229human GRCh38 chr16: 25,128,816-25,129,102 , GRCh37.p13 chr16: 25,140,137-25,140,423 LCMT1
    nsv6987227copy number variation1nstd229human GRCh38 chr16: 25,109,801-25,115,000 , GRCh37.p13 chr16: 25,121,122-25,126,321 LCMT1, LCMT1-AS1
    nsv6984393copy number variation1nstd229human GRCh38 chr16: 25,099,702-25,109,713 , GRCh37.p13 chr16: 25,111,023-25,121,034 LCMT1-AS1, LCMT1
    nsv6637633copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,576,803-30,177,240 , GRCh38.p12 chr16: 21,565,482-30,165,919 USP31, CA5AP1, 200 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    nsv6593707inversion1nstd223human GRCh38 chr16: 25,162,983-25,163,453 , GRCh37.p13 chr16: 25,174,304-25,174,774 LCMT1
    nsv6586886inversion1nstd223human GRCh38 chr16: 25,161,357-25,162,432 , GRCh37.p13 chr16: 25,172,678-25,173,753 LCMT1
    nsv6580577inversion1nstd223human GRCh38 chr16: 25,133,409-25,133,923 , GRCh37.p13 chr16: 25,144,730-25,145,244 LCMT1
    nsv6578695inversion1nstd223human GRCh38 chr16: 25,149,634-25,150,642 , GRCh37.p13 chr16: 25,160,955-25,161,963 LCMT1
    nsv6577036inversion1nstd223human GRCh38 chr16: 25,153,855-25,154,068 , GRCh37.p13 chr16: 25,165,176-25,165,389 LCMT1
    nsv6507059copy number variation1nstd223human GRCh38 chr16: 25,113,048-25,120,147 , GRCh37.p13 chr16: 25,124,369-25,131,468 LCMT1
    nsv6505130copy number variation1nstd223human GRCh38 chr16: 25,176,704-25,179,042 , GRCh37.p13 chr16: 25,188,025-25,190,363 LCMT1
    nsv6290289copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,594,997-29,625,302 , GRCh38.p12 chr16: 21,583,676-29,613,981 LOC105371149, SLX1B, 166 more genes
    nsv6289847copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,530,207-29,332,245 , GRCh38.p12 chr16: 21,518,886-29,320,924 GAPDHP35, NSMCE1, 154 more genes
    nsv6144430copy number variation1nstd206human GRCh38 chr16: 25,054,486-25,126,486 , GRCh37.p13 chr16: 25,065,807-25,137,807 LCMT1, LINC02175, 4 more genes
    nsv6133272copy number variation1nstd213human GRCh37 chr16: 24,980,000-25,140,001 , GRCh38.p12 chr16: 24,968,679-25,128,680 LCMT1, ARHGAP17, 7 more genes
    nsv6133268copy number variation1nstd213human GRCh37 chr16: 22,710,000-32,010,001 , GRCh38.p12 chr16: 22,698,679-31,998,680 ALDOA, AQP8, 269 more genes
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