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Items: 1 to 20 of 109

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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
    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
    nsv4456092copy number variation1nstd102humanUncertain significance GRCh37 chr16: 66,797,153-67,109,495 , GRCh38.p12 chr16: 66,763,250-67,075,592 CES4A, RN7SL543P, 12 more genes
    nsv4455939copy number variation1nstd102humanUncertain significance GRCh37 chr16: 66,876,199-67,150,370 , GRCh38.p12 chr16: 66,842,296-67,116,467 CDH16, CA7, 11 more genes
    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
    nsv4237582copy number variation1nstd166human GRCh37.p13 chr16: 66,968,614-66,972,072 , GRCh38.p12 chr16: 66,934,711-66,938,169 CES2, CIAO2B
    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
    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
    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
    nsv3918405copy number variation1nstd102humanPathogenic GRCh38 chr16: 66,245,888-67,473,023 , NCBI36 chr16: 64,837,292-66,064,427 , GRCh37 chr16: 66,279,791-67,506,926 PLEKHG4, TMEM208, 53 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
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