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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
    nsv5970379inversion1nstd209human GRCh38 chr16: 1,516,497-2,069,901 , GRCh37.p13 chr16: 1,566,498-2,119,902 GFER, HAGH, 37 more genes
    nsv5929910copy number variation1nstd209human GRCh38 chr16: 1,773,460-1,773,764 , GRCh37.p13 chr16: 1,823,461-1,823,765 EME2, MRPS34
    nsv5380998copy number variation2nstd102humanUncertain significance GRCh37 chr16: 624,055-2,153,916 , GRCh38.p12 chr16: 574,055-2,103,915 NDUFB10, BAIAP3, 102 more genes
    nsv5311960copy number variation1nstd204human GRCh37.p13 chr16: 1,823,440-1,823,788 , GRCh38.p13 chr16: 1,773,439-1,773,787 EME2, MRPS34
    nsv5271137copy number variation1nstd204human GRCh38.p13 chr16: 1,615,401-2,135,300 , GRCh37.p13 chr16: 1,665,402-2,185,301 SNHG9, SNORA64, 40 more genes
    nsv5270514copy number variation1nstd204human GRCh38.p13 chr16: 1,765,392-1,777,341 , GRCh37.p13 chr16: 1,815,393-1,827,342 EME2, MRPS34, 3 more genes
    nsv5269318copy number variation1nstd204human GRCh38.p13 chr16: 1,733,301-3,469,700 , GRCh37.p13 chr16: 1,783,302-3,519,700 , MIR6511B1, 156 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
    nsv5007892copy number variation1nstd200human GRCh38 chr16: 1,772,257-1,772,318 , GRCh37.p13 chr16: 1,822,258-1,822,319 MRPS34, EME2
    nsv5007891copy number variation1nstd200human GRCh38 chr16: 1,771,177-1,825,930 , GRCh37.p13 chr16: 1,821,178-1,875,931 HAGH, IGFALS, 6 more genes
    nsv4866374copy number variation1nstd200human GRCh37 chr16: 1,823,465-1,823,766 , GRCh38.p12 chr16: 1,773,464-1,773,765 EME2, MRPS34
    nsv4729241copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-5,249,457 , GRCh38.p12 chr16: 35,880-5,199,456 MTRNR2L4, BRICD5, 307 more genes
    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
    nsv4682253copy number variation1nstd102humanPathogenic GRCh37 chr16: 1,573,499-2,114,448 , GRCh38.p12 chr16: 1,523,498-2,064,447 NHERF2, IGFALS, 37 more genes
    nsv4631014copy number variation1nstd183human GRCh37 chr16: 1,820,976-1,823,351 , GRCh38.p12 chr16: 1,770,975-1,773,350 EME2, NME3, 1 more genes
    nsv4626758copy number variation1nstd183human GRCh37 chr16: 1,820,976-1,821,400 , GRCh38.p12 chr16: 1,770,975-1,771,399 NME3, MRPS34, 1 more genes
    nsv4622757copy number variation1nstd183human GRCh37 chr16: 1,822,244-1,823,743 , GRCh38.p12 chr16: 1,772,243-1,773,742 NME3, EME2, 1 more genes
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