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Items: 1 to 20 of 134

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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
    nsv7094777copy number variation1nstd102humanPathogenic GRCh37 chr16: 27,441,393-29,001,333 , GRCh38.p12 chr16: 27,430,072-28,990,012 NUPR1, RPS15AP33, 45 more genes
    nsv7094776copy number variation1nstd102humanUncertain significance GRCh37 chr16: 27,441,393-28,899,063 , GRCh38.p12 chr16: 27,430,072-28,887,742 SH2B1, RNU6-1241P, 39 more genes
    nsv7074538inversion1nstd229human GRCh38 chr16: 28,237,866-28,246,368 , GRCh37.p13 chr16: 28,249,187-28,257,689 GAPDHP35
    nsv6997991copy number variation1nstd229human GRCh38 chr16: 28,235,065-28,251,332 , GRCh37.p13 chr16: 28,246,386-28,262,653 GAPDHP35
    nsv6994025copy number variation1nstd229human GRCh38 chr16: 28,226,823-28,280,970 , GRCh37.p13 chr16: 28,238,144-28,292,291 GAPDHP35, SBK1
    nsv6991839copy number variation1nstd229human GRCh38 chr16: 28,235,444-28,282,229 , GRCh37.p13 chr16: 28,246,765-28,293,550 GAPDHP35, SBK1
    nsv6990277copy number variation1nstd229human GRCh38 chr16: 28,236,619-28,253,108 , GRCh37.p13 chr16: 28,247,940-28,264,429 GAPDHP35
    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
    nsv6623582copy number variation1nstd224human GRCh37 chr16: 28,137,151-28,264,210 , GRCh38.p12 chr16: 28,125,830-28,252,889 GAPDHP35, XPO6, 1 more genes
    nsv6582293inversion1nstd223human GRCh38 chr16: 28,240,941-28,241,294 , GRCh37.p13 chr16: 28,252,262-28,252,615 GAPDHP35
    nsv6507284copy number variation1nstd223human GRCh38 chr16: 28,217,923-28,240,835 , GRCh37.p13 chr16: 28,229,244-28,252,156 GAPDHP35
    nsv6506382copy number variation1nstd223human GRCh38 chr16: 28,116,939-28,259,277 , GRCh37.p13 chr16: 28,128,260-28,270,598 RNY1P10, XPO6, 2 more genes
    nsv6503603copy number variation1nstd223human GRCh38 chr16: 28,228,057-28,242,938 , GRCh37.p13 chr16: 28,239,378-28,254,259 GAPDHP35
    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
    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
    nsv6133019copy number variation1nstd213human GRCh37 chr16: 27,940,000-28,670,001 , GRCh38.p12 chr16: 27,928,679-28,658,680 CLN3, SULT1A2, 19 more genes
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