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Items: 1 to 20 of 138

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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
    nsv7073753inversion1nstd229human GRCh38 chr16: 25,011,074-25,020,050 , GRCh37.p13 chr16: 25,022,395-25,031,371 ARHGAP17, LOC100421171
    nsv7069781inversion1nstd229human GRCh38 chr16: 24,962,563-25,492,782 , GRCh37.p13 chr16: 24,973,884-25,504,103 CYCSP39, ARHGAP17, 13 more genes
    nsv6997862copy number variation1nstd229human GRCh38 chr16: 25,017,886-25,023,796 , GRCh37.p13 chr16: 25,029,207-25,035,117 LOC100421171
    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
    nsv6594879inversion1nstd223human GRCh38 chr16: 25,013,917-25,014,938 , GRCh37.p13 chr16: 25,025,238-25,026,259 ARHGAP17, LOC100421171
    nsv6582990inversion1nstd223human GRCh38 chr16: 25,022,156-25,022,245 , GRCh37.p13 chr16: 25,033,477-25,033,566 LOC100421171
    nsv6578093inversion1nstd223human GRCh38 chr16: 25,021,923-25,022,518 , GRCh37.p13 chr16: 25,033,244-25,033,839 LOC100421171
    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
    nsv6272519copy number variation1nstd214human GRCh38 chr16: 25,021,365-25,021,416 , GRCh37.p13 chr16: 25,032,686-25,032,737 LOC100421171
    nsv6206125copy number variation1nstd214human GRCh38 chr16: 25,021,293-25,021,362 , GRCh37.p13 chr16: 25,032,614-25,032,683 LOC100421171
    nsv6204628copy number variation1nstd214human GRCh38 chr16: 25,021,347-25,021,416 , GRCh37.p13 chr16: 25,032,668-25,032,737 LOC100421171
    nsv6203567copy number variation1nstd214human GRCh38 chr16: 25,021,295-25,021,345 , GRCh37.p13 chr16: 25,032,616-25,032,666 LOC100421171
    nsv6198202copy number variation1nstd214human GRCh38 chr16: 25,021,293-25,021,344 , GRCh37.p13 chr16: 25,032,614-25,032,665 LOC100421171
    nsv6197092copy number variation1nstd214human GRCh38 chr16: 25,021,293-25,021,363 , GRCh37.p13 chr16: 25,032,614-25,032,684 LOC100421171
    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
    nsv6133267copy number variation1nstd213human GRCh37 chr16: 22,710,000-30,200,001 , GRCh38.p12 chr16: 22,698,679-30,188,680 ALDOA, AQP8, 169 more genes
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