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Items: 1 to 20 of 115

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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
    nsv7061059inversion1nstd229human GRCh38 chr16: 23,459,969-24,877,943 , GRCh37.p13 chr16: 23,471,290-24,889,264 LOC105371143, CHP2, 20 more genes
    nsv7060602inversion1nstd229human GRCh38 chr16: 22,087,809-24,116,610 , GRCh37.p13 chr16: 22,099,130-24,127,931 RRN3P3, MFSD13B, 34 more genes
    nsv6996099copy number variation1nstd229human GRCh38 chr16: 23,725,916-23,762,541 , GRCh37.p13 chr16: 23,737,237-23,773,862 CHP2
    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
    nsv6623387copy number variation1nstd224human GRCh37 chr16: 23,717,833-23,815,361 , GRCh38.p12 chr16: 23,706,512-23,804,040 ERN2, CHP2
    nsv6508632copy number variation1nstd223human GRCh38 chr16: 23,737,666-23,783,955 , GRCh37.p13 chr16: 23,748,987-23,795,276 CHP2
    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
    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
    nsv6133189copy number variation1nstd213human GRCh37 chr16: 23,660,000-23,860,001 , GRCh38.p12 chr16: 23,648,679-23,848,680 PLK1, PRKCB, 3 more genes
    nsv5929387copy number variation1nstd209human GRCh38 chr16: 20,698,055-24,692,430 , GRCh37.p13 chr16: 20,709,377-24,703,751 , ACSM1, 87 more genes
    nsv5274402copy number variation1nstd204human GRCh38.p13 chr16: 23,737,701-23,784,000 , GRCh37.p13 chr16: 23,749,022-23,795,321 CHP2
    nsv5266216copy number variation1nstd204human GRCh38.p13 chr16: 23,750,826-23,783,740 , GRCh37.p13 chr16: 23,762,147-23,795,061 CHP2
    nsv5003211copy number variation1nstd200human GRCh38 chr16: 23,756,468-23,758,671 , GRCh37.p13 chr16: 23,767,789-23,769,992 CHP2
    nsv4850751copy number variation1nstd200human GRCh37 chr16: 23,767,789-23,769,992 , GRCh38.p12 chr16: 23,756,468-23,758,671 CHP2
    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
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