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Items: 1 to 20 of 152

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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
    nsv5971532insertion1nstd209human GRCh38 chr16: 3,393,227-3,393,227 , GRCh37.p13 chr16: 3,443,227-3,443,227 LOC105371059, ZSCAN32
    nsv5654733insertion2nstd207human GRCh38 chr16: 3,393,202-3,393,202 , GRCh37.p13 chr16: 3,443,202-3,443,202 ZSCAN32, LOC105371059
    nsv5649810insertion1nstd207human GRCh38 chr16: 3,393,239-3,393,239 , GRCh37.p13 chr16: 3,443,239-3,443,239 LOC105371059, ZSCAN32
    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
    nsv5140572mobile element insertion1nstd203human GRCh38 chr16: 3,392,825-3,392,841 , GRCh37.p13 chr16: 3,442,825-3,442,841 LOC105371059, ZSCAN32
    nsv5008000copy number variation1nstd200human GRCh38 chr16: 3,327,719-3,398,127 , GRCh37.p13 chr16: 3,377,719-3,448,127 OR2C1, ZSCAN32, 6 more genes
    nsv4866459copy number variation1nstd200human GRCh37 chr16: 3,377,719-3,448,127 , GRCh38.p12 chr16: 3,327,719-3,398,127 OR2C1, ZSCAN32, 6 more genes
    nsv4757884insertion1nstd199human GRCh37 chr16: 3,443,191-3,443,191 , GRCh38.p12 chr16: 3,393,191-3,393,191 ZSCAN32, LOC105371059
    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
    nsv4729241copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-5,249,457 , GRCh38.p12 chr16: 35,880-5,199,456 MTRNR2L4, BRICD5, 307 more genes
    nsv4675826copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,651,354-4,614,965 , GRCh38.p12 chr16: 2,601,353-4,564,964 MEFV, TRR-CCT5-1, 111 more genes
    nsv4632133copy number variation1nstd183human GRCh37 chr16: 3,445,074-3,445,153 , GRCh38.p12 chr16: 3,395,074-3,395,153 LOC105371059, ZSCAN32
    nsv4619221copy number variation1nstd183human GRCh37 chr16: 3,432,155-3,433,840 , GRCh38.p12 chr16: 3,382,155-3,383,840 LOC105371059, ZSCAN32
    nsv4544513insertion1nstd166human GRCh37.p13 chr16: 3,443,170-3,443,170 , GRCh38.p12 chr16: 3,393,170-3,393,170 LOC105371059, ZSCAN32
    nsv4542498insertion1nstd166human GRCh37.p13 chr16: 3,443,241-3,443,241 , GRCh38.p12 chr16: 3,393,241-3,393,241 LOC105371059, ZSCAN32
    nsv4456418copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,112,024-3,738,078 , GRCh38.p12 chr16: 3,062,023-3,688,077 ZNF597, ZNF205-AS1, 55 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
    nsv4247873copy number variation1nstd166human GRCh37.p13 chr16: 3,443,608-3,444,459 , GRCh38.p12 chr16: 3,393,608-3,394,459 ZSCAN32, LOC105371059
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