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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5158635mobile element insertion1nstd203human GRCh38 chr16: 67,237,397-67,237,411 , GRCh37.p13 chr16: 67,271,300-67,271,314 FHOD1
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv4993096copy number variation1nstd200human GRCh38 chr16: 67,235,984-67,236,082 , GRCh37.p13 chr16: 67,269,887-67,269,985 FHOD1
    nsv4993095copy number variation1nstd200human GRCh38 chr16: 67,228,585-67,249,440 , GRCh37.p13 chr16: 67,262,488-67,283,343 SLC9A5, TMEM208, 1 more genes
    nsv4878809inversion1nstd200human GRCh37 chr16: 60,132,255-77,533,939 , GRCh38.p12 chr16: 60,098,351-77,500,042 , ST3GAL2, 313 more genes
    nsv4857469copy number variation1nstd200human GRCh37 chr16: 67,269,887-67,269,985 , GRCh38.p12 chr16: 67,235,984-67,236,082 FHOD1
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 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
    nsv4630558copy number variation1nstd183human GRCh37 chr16: 67,262,506-67,262,550 , GRCh38.p12 chr16: 67,228,603-67,228,647 FHOD1, TMEM208
    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
    nsv4423203copy number variation1nstd174human GRCh37 chr16: 67,175,101-67,323,199 , GRCh38.p12 chr16: 67,141,198-67,289,296 EXOC3L1, MIR328, 15 more genes
    nsv4350223copy number variation1nstd102humanPathogenic GRCh37 chr16: 67,132,790-68,166,320 , GRCh38.p12 chr16: 67,098,887-68,132,417 CBFB, B3GNT9, 55 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
    nsv3924078copy number variation1nstd102humanUncertain significance NCBI36 chr16: 65,484,671-66,350,189 , GRCh37.p13 chr16: 66,927,170-67,792,688 , GRCh38.p12 chr16: 66,893,267-67,758,785 ENKD1, LOC100505942, 45 more genes
    nsv3923741copy number variation1nstd102humanUncertain significance GRCh37 chr16: 66,927,107-67,391,081 , GRCh38 chr16: 66,893,204-67,357,178 , NCBI36 chr16: 65,484,608-65,948,582 CIAO2B, EXOC3L1, 27 more genes
    nsv3923505copy number variation1nstd102humanPathogenic NCBI36 chr16: 65,285,584-66,456,849 , GRCh37 chr16: 66,728,083-67,899,348 , GRCh38 chr16: 66,694,180-67,865,445 DYNC1LI2, CIAO2B, 56 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
    nsv3920667copy number variation1nstd102humanUncertain significance NCBI36 chr16: 65,513,073-65,903,848 , GRCh38 chr16: 66,921,669-67,312,444 , GRCh37 chr16: 66,955,572-67,346,347 PLEKHG4, TMEM208, 23 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
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