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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094683copy number variation1nstd102humanUncertain significance GRCh37 chr16: 65,821,800-72,146,396 , GRCh38.p12 chr16: 65,787,897-72,112,497 TRG-GCC5-1, RNU6-359P, 205 more genes
    nsv7094682copy number variation2nstd102humanPathogenic GRCh37 chr16: 65,821,800-67,208,957 , GRCh38.p12 chr16: 65,787,897-67,175,054 RNA5SP428, PHAF1, 38 more genes
    nsv6990340copy number variation1nstd229human GRCh38 chr16: 66,732,301-67,029,000 , GRCh37.p13 chr16: 66,766,204-67,062,903 DYNC1LI2-DT, NAE1, 14 more genes
    nsv6990199copy number variation1nstd229human GRCh38 chr16: 66,934,711-66,938,174 , GRCh37.p13 chr16: 66,968,614-66,972,077 CIAO2B, CES2
    nsv6979396copy number variation1nstd229human GRCh38 chr16: 66,841,465-67,115,793 , GRCh37.p13 chr16: 66,875,368-67,149,696 CBFB, CDH16, 11 more genes
    nsv6508640copy number variation1nstd223human GRCh38 chr16: 66,934,707-66,938,169 , GRCh37.p13 chr16: 66,968,610-66,972,072 CIAO2B, CES2
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    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
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