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Items: 1 to 20 of 113

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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
    nsv6994230copy number variation1nstd229human GRCh38 chr16: 25,064,945-25,067,603 , GRCh37.p13 chr16: 25,076,266-25,078,924 SCML2P2, LINC02175
    nsv6991377copy number variation1nstd229human GRCh38 chr16: 25,066,785-25,071,699 , GRCh37.p13 chr16: 25,078,106-25,083,020 LINC02175, LOC100421169, 1 more genes
    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
    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
    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
    nsv6133266copy number variation1nstd213human GRCh37 chr16: 22,710,000-26,360,001 , GRCh38.p12 chr16: 22,698,679-26,348,680 AQP8, NDUFAB1, 54 more genes
    nsv5003266copy number variation1nstd200human GRCh38 chr16: 25,064,945-25,067,599 , GRCh37.p13 chr16: 25,076,266-25,078,920 LINC02175, SCML2P2
    nsv4900137mobile element deletion1nstd200human GRCh38 chr16: 25,068,958-25,069,093 , GRCh37.p13 chr16: 25,080,279-25,080,414 SCML2P2, LINC02175
    nsv4850797copy number variation1nstd200human GRCh37 chr16: 25,076,916-25,076,984 , GRCh38.p12 chr16: 25,065,595-25,065,663 LINC02175
    nsv4850796copy number variation1nstd200human GRCh37 chr16: 25,076,265-25,078,920 , GRCh38.p12 chr16: 25,064,944-25,067,599 LINC02175, SCML2P2
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 NPIPB9, TMEM219, 597 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 LOC105371069, PKD1P6-NPIPP1, 654 more genes
    nsv4685761copy number variation1nstd102humannot provided GRCh37 chr16: 21,312,200-29,646,379 , GRCh38.p12 chr16: 21,300,879-29,635,058 NUPR1, TNRC6A, 176 more genes
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