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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
    nsv5380995copy number variation1nstd102humanUncertain significance GRCh37 chr16: 2,098,597-2,550,979 , GRCh38.p12 chr16: 2,048,596-2,500,978 TEDC2, MIR3677HG, 33 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
    nsv5266471copy number variation1nstd204human GRCh38.p13 chr16: 1,936,501-2,552,200 , GRCh37.p13 chr16: 1,986,502-2,602,201 AMDHD2, MIR3178, 56 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
    nsv5007910copy number variation1nstd200human GRCh38 chr16: 2,152,944-2,153,053 , GRCh37.p13 chr16: 2,202,945-2,203,054 SNORD60, RAB26, 1 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
    nsv4716573copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,157,801-2,288,100 , GRCh38.p12 chr16: 2,107,800-2,238,099 MIR3180-5, BRICD5, 12 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
    nsv4675023copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,162,341-2,203,046 , GRCh38.p12 chr16: 2,112,340-2,153,045 PKD1, RAB26, 4 more genes
    nsv4620933copy number variation1nstd183human GRCh37 chr16: 2,097,158-2,237,846 , GRCh38.p12 chr16: 2,047,157-2,187,845 TRAF7, RAB26, 11 more genes
    nsv4457206copy number variation1nstd102humanUncertain significance GRCh37 chr16: 2,070,917-2,592,737 , GRCh38.p12 chr16: 2,020,916-2,542,736 CEMP1, MIR3180-5, 41 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
    nsv4375182copy number variation1nstd173human GRCh37 chr16: 2,156,160-2,220,764 , GRCh38.p12 chr16: 2,106,159-2,170,763 PKD1, TRAF7, 6 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
    nsv3923267copy number variation1nstd102humanPathogenic GRCh37 chr16: 93,732-13,420,663 , GRCh38 chr16: 43,732-13,326,806 , NCBI36 chr16: 33,732-13,328,164 METRN, FAM234A, 413 more genes
    nsv3923184copy number variation1nstd102humanPathogenic GRCh37 chr16: 96,766-3,264,623 , GRCh38 chr16: 46,766-3,214,623 , NCBI36 chr16: 36,766-3,204,624 TRP-CGG1-2, HAGHL, 235 more genes
    nsv3920144copy number variation1nstd102humanUncertain significance NCBI36 chr16: 2,123,686-2,216,665 , GRCh37.p13 chr16: 2,183,685-2,276,664 , GRCh38.p12 chr16: 2,133,684-2,226,663 BRICD5, MLST8, 10 more genes
    nsv3918246copy number variation1nstd102humanPathogenic NCBI36 chr16: 19,941-2,550,462 , GRCh38 chr16: 29,941-2,560,460 , GRCh37 chr16: 79,941-2,610,461 TEDC2, SYNGR3, 172 more genes
    nsv3917929copy number variation1nstd102humanPathogenic GRCh37 chr16: 96,766-11,619,372 , GRCh38 chr16: 46,766-11,525,516 , NCBI36 chr16: 36,766-11,526,873 LOC100130283, PGP, 386 more genes
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