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Items: 1 to 20 of 93

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5527869copy number variation1nstd206human GRCh38 chr16: 55,567,360-55,567,410 , GRCh37.p13 chr16: 55,601,272-55,601,322 LPCAT2, CAPNS2
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4514654mobile element insertion1nstd166human GRCh37.p13 chr16: 55,599,748-55,599,748 , GRCh38.p12 chr16: 55,565,836-55,565,836 CAPNS2, LPCAT2
    nsv4456077copy number variation1nstd102humanUncertain significance GRCh37 chr16: 53,455,650-64,006,604 , GRCh38.p12 chr16: 53,421,738-63,972,700 MT1DP, RPL23AP91, 167 more genes
    nsv4365843copy number variation1nstd173human GRCh37 chr16: 46,464,489-55,795,214 , GRCh38.p12 chr16: 46,430,577-55,761,302 , LOC100526838, 158 more genes
    nsv4365186copy number variation1nstd173human GRCh37 chr16: 46,503,205-57,376,253 , GRCh38.p12 chr16: 46,469,293-57,342,341 , TOX3, 210 more genes
    nsv4241354copy number variation1nstd166human GRCh37.p13 chr16: 55,583,549-55,636,416 , GRCh38.p12 chr16: 55,549,637-55,602,504 CAPNS2, LPCAT2
    nsv3921269copy number variation1nstd102humanPathogenic NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 LOC105371237, IGHV3OR16-11, 985 more genes
    nsv3918594copy number variation1nstd102humanPathogenic GRCh38 chr16: 50,784,329-55,566,715 , NCBI36 chr16: 49,375,741-54,158,128 , GRCh37 chr16: 50,818,240-55,600,627 TOX3, CASC22, 74 more genes
    nsv3918521copy number variation1nstd102humanPathogenic NCBI36 chr16: 48,276,933-66,993,116 , GRCh37 chr16: 49,719,432-68,435,615 , GRCh38 chr16: 49,685,521-68,401,712 CYLD-AS2, MT1F, 342 more genes
    nsv3917427copy number variation1nstd102humanBenign NCBI36 chr16: 32,529,496-88,822,254 , GRCh37.p13 chr16: 32,621,995-90,294,753 , GRCh38.p12 chr16: 32,610,674-90,228,345 TXNL4B, KLHL36, 968 more genes
    nsv3916905copy number variation1nstd102humanBenign NCBI36 chr16: 32,481,314-88,822,254 , GRCh37.p13 chr16: 32,573,813-90,294,753 , GRCh38.p12 chr16: 32,562,492-90,228,345 CDH16, TP53TG3HP, 968 more genes
    nsv3916542copy number variation1nstd102humanPathogenic GRCh38 chr16: 55,457,477-63,841,622 , NCBI36 chr16: 54,048,890-62,433,027 , GRCh37 chr16: 55,491,389-63,875,526 CES1, SNORA46, 139 more genes
    nsv3915506copy number variation1nstd102humanPathogenic NCBI36 chr16: 51,490,596-88,682,563 , GRCh38 chr16: 52,899,183-90,088,654 , GRCh37 chr16: 52,933,095-90,155,062 CFAP69P1, GAS8-AS1, 716 more genes
    nsv3915341copy number variation1nstd102humanBenign NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 GINS3, LINC00919, 985 more genes
    nsv3915118copy number variation1nstd102humanBenign NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 ZFHX3, CENPN-AS1, 985 more genes
    nsv3912769copy number variation1nstd102humanBenign NCBI36 chr16: 31,862,658-88,822,254 , GRCh37.p13 chr16: 31,955,157-90,294,753 , GRCh38.p12 chr16: 31,943,836-90,228,345 MAF, LOC112268167, 985 more genes
    nsv3912663copy number variation1nstd102humanBenign NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 SMG1P7, LOC105371287, 985 more genes
    nsv3912156copy number variation1nstd102humanBenign NCBI36 chr16: 31,902,168-88,822,254 , GRCh37.p13 chr16: 31,994,667-90,294,753 , GRCh38.p12 chr16: 31,983,346-90,228,345 IST1, CMTR2, 985 more genes
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