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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv4878809inversion1nstd200human GRCh37 chr16: 60,132,255-77,533,939 , GRCh38.p12 chr16: 60,098,351-77,500,042 , ST3GAL2, 313 more genes
    nsv4857550copy number variation1nstd200human GRCh37 chr16: 69,600,124-69,600,174 , GRCh38.p12 chr16: 69,566,221-69,566,271 NFAT5, MIR1538
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729943copy number variation1nstd102humanUncertain significance GRCh37 chr16: 69,369,131-69,942,990 , GRCh38.p12 chr16: 69,335,228-69,909,087 NIP7, CYB5B, 12 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4675201copy number variation1nstd102humanPathogenic GRCh37 chr16: 65,669,673-70,180,183 , GRCh38.p12 chr16: 65,635,770-70,146,280 LOC100420066, LINC00920, 143 more genes
    nsv4628233copy number variation1nstd183human GRCh37 chr16: 69,595,761-69,617,045 , GRCh38.p12 chr16: 69,561,858-69,583,142 MIR1538, NFAT5
    nsv4436581complex substitution1nstd102humanUncertain significance GRCh38.p12 chr16: 56,334,777-90,074,947 , GRCh37 chr16: 56,368,689-90,141,355 AARS1, AP1G1, 662 more genes
    nsv4332560sequence alteration1nstd166human GRCh37.p13 chr16: 57,901,049-75,540,778 , GRCh38.p12 chr16: 57,867,145-75,506,880 , AGRP, 331 more genes
    nsv4321328inversion1nstd166human GRCh37.p13 chr16: 67,701,568-75,754,137 , GRCh38.p12 chr16: 67,667,665-75,720,239 , CDH3, 203 more genes
    nsv4232747copy number variation1nstd166human GRCh37.p13 chr16: 69,600,124-69,600,174 , GRCh38.p12 chr16: 69,566,221-69,566,271 NFAT5, MIR1538
    nsv3922126copy number variation1nstd102humanPathogenic NCBI36 chr16: 67,644,861-81,865,787 , GRCh38 chr16: 69,053,457-83,274,681 , GRCh37 chr16: 69,087,360-83,308,286 LOC105371357, EXOSC6, 232 more genes
    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
    nsv3920399copy number variation1nstd102humanPathogenic NCBI36 chr16: 61,517,334-83,176,902 , GRCh37 chr16: 62,959,833-84,619,401 , GRCh38 chr16: 62,925,929-84,585,795 LOC654780, LSM3P5, 385 more genes
    nsv3919817copy number variation1nstd102humanPathogenic NCBI36 chr16: 63,904,799-88,675,894 , GRCh37 chr16: 65,347,298-90,148,393 , GRCh38 chr16: 65,313,395-90,081,985 LOC105376772, WWP2, 527 more genes
    nsv3917492copy number variation1nstd102humanPathogenic NCBI36 chr16: 64,549,233-82,202,549 , GRCh38 chr16: 65,957,829-83,611,443 , GRCh37 chr16: 65,991,732-83,645,048 ELMO3, SNORD71, 346 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
    nsv3916803copy number variation1nstd102humanPathogenic NCBI36 chr16: 68,126,727-74,517,697 , GRCh37.p13 chr16: 69,569,226-75,960,196 , GRCh38.p12 chr16: 69,535,323-75,926,298 AP1G1, CPHXL, 138 more genes
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