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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5947462copy number variation1nstd209human GRCh38 chr16: 1,438,383-1,438,645 , GRCh37.p13 chr16: 1,488,384-1,488,646 CCDC154
    nsv5524805copy number variation1nstd206human GRCh38 chr16: 1,437,743-1,437,798 , GRCh37.p13 chr16: 1,487,744-1,487,799 CCDC154
    nsv5380998copy number variation2nstd102humanUncertain significance GRCh37 chr16: 624,055-2,153,916 , GRCh38.p12 chr16: 574,055-2,103,915 NDUFB10, BAIAP3, 102 more genes
    nsv5278705copy number variation1nstd204human GRCh38.p13 chr16: 1,376,101-1,511,800 , GRCh37.p13 chr16: 1,426,102-1,561,801 UNKL, IFT140, 9 more genes
    nsv5278593copy number variation1nstd204human GRCh38.p13 chr16: 495,101-1,599,500 , GRCh37.p13 chr16: 545,101-1,649,501 , MIR662, 73 more genes
    nsv5265522copy number variation1nstd204human GRCh38.p13 chr16: 53,201-2,576,200 , GRCh37.p13 chr16: 103,201-2,626,201 , RHBDL1, 175 more genes
    nsv4729673copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,233,996-1,509,217 , GRCh38.p12 chr16: 1,183,996-1,459,216 LOC105371044, TPSB2, 19 more genes
    nsv4729241copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-5,249,457 , GRCh38.p12 chr16: 35,880-5,199,456 MTRNR2L4, BRICD5, 307 more genes
    nsv4727872copy number variation2nstd197human GRCh38.p12 chr16: 1,438,620-1,442,975 , GRCh37 chr16: 1,488,621-1,492,976 CLCN7, CCDC154
    nsv4683390copy number variation1nstd102humanPathogenic GRCh37 chr16: 624,055-2,148,005 , GRCh38.p12 chr16: 574,055-2,098,004 MRPS34, HAGHL, 102 more genes
    nsv4683209copy number variation1nstd102humanPathogenic GRCh37 chr16: 1,203,718-2,185,710 , GRCh38.p12 chr16: 1,153,718-2,135,709 TMEM204, UQCC4, 67 more genes
    nsv4682518copy number variation1nstd102humanUncertain significance GRCh37 chr16: 624,055-2,550,979 , GRCh38.p12 chr16: 574,055-2,500,978 C1QTNF8, NHERF2, 133 more genes
    nsv4542548insertion1nstd166human GRCh37.p13 chr16: 1,490,443-1,490,443 , GRCh38.p12 chr16: 1,440,442-1,440,442 CCDC154
    nsv4532583copy number variation1nstd166human GRCh37.p13 chr16: 1,483,456-1,483,867 , GRCh38.p12 chr16: 1,433,455-1,433,866 CCDC154, PERCC1
    nsv4455594copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-2,053,328 , GRCh38.p12 chr16: 35,880-2,003,327 JPT2, TSR3, 128 more genes
    nsv4449893copy number variation1nstd102humanPathogenic GRCh37 chr16: 624,055-2,115,656 , GRCh38.p12 chr16: 574,055-2,065,655 LMF1-AS1, RAB40C, 99 more genes
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ABAT, ABCA3, 876 more genes
    nsv4349832copy number variation1nstd102humanPathogenic GRCh37 chr16: 109,978-4,316,797 , GRCh38.p12 chr16: 59,980-4,266,796 LINC00235, RNF151, 269 more genes
    nsv4334280sequence alteration1nstd166human GRCh38.p12 chr16: 1,436,691-1,519,077 , GRCh37.p13 chr16: 1,486,692-1,569,078 CLCN7, IFT140, 4 more genes
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