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Items: 1 to 20 of 107

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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
    nsv6992934copy number variation1nstd229human GRCh38 chr16: 66,551,201-66,643,300 , GRCh37.p13 chr16: 66,585,104-66,677,203 CMTM3, CKLF-CMTM1, 4 more genes
    nsv6990600copy number variation1nstd229human GRCh38 chr16: 66,444,868-66,662,149 , GRCh37.p13 chr16: 66,478,771-66,696,052 TK2, CMTM2, 8 more genes
    nsv6585759inversion1nstd223human GRCh38 chr16: 66,602,350-66,602,806 , GRCh37.p13 chr16: 66,636,253-66,636,709 CMTM4, CMTM3
    nsv6509129copy number variation1nstd223human GRCh38 chr16: 66,601,786-66,606,079 , GRCh37.p13 chr16: 66,635,689-66,639,982 CMTM4, CMTM3
    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
    nsv5525317copy number variation1nstd206human GRCh38 chr16: 66,608,862-66,609,025 , GRCh37.p13 chr16: 66,642,765-66,642,928 CMTM4, CMTM3
    nsv5515731copy number variation1nstd206human GRCh38 chr16: 66,605,434-66,605,541 , GRCh37.p13 chr16: 66,639,337-66,639,444 CMTM3, CMTM4
    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
    nsv4857450copy number variation1nstd200human GRCh37 chr16: 66,642,765-66,642,928 , GRCh38.p12 chr16: 66,608,862-66,609,025 CMTM4, CMTM3
    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
    nsv4578635copy number variation1nstd102humanUncertain significance GRCh37 chr16: 64,981,506-66,806,661 , GRCh38.p12 chr16: 64,947,603-66,772,758 CKLF-CMTM1, BEAN1, 21 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
    nsv4239786copy number variation1nstd166human GRCh37.p13 chr16: 66,642,765-66,642,928 , GRCh38.p12 chr16: 66,608,862-66,609,025 CMTM4, CMTM3
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