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Items: 1 to 20 of 147

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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
    nsv7075084inversion1nstd229human GRCh38 chr16: 67,127,296-73,957,488 , GRCh37.p13 chr16: 67,161,199-73,991,387 MIR1538, LINC02136, 187 more genes
    nsv6993386copy number variation1nstd229human GRCh38 chr16: 67,178,001-67,193,100 , GRCh37.p13 chr16: 67,211,904-67,227,003 EXOC3L1, MATCAP1, 1 more genes
    nsv6987699copy number variation1nstd229human GRCh38 chr16: 67,178,586-67,199,277 , GRCh37.p13 chr16: 67,212,489-67,233,180 MATCAP1, ELMO3, 2 more genes
    nsv6981317copy number variation1nstd229human GRCh38 chr16: 67,182,817-67,183,104 , GRCh37.p13 chr16: 67,216,720-67,217,007 EXOC3L1, MATCAP1
    nsv6636055copy number variation1nstd102humanUncertain significance GRCh37 chr16: 67,208,681-67,208,734 , GRCh38 chr16: 67,174,778-67,174,831 NOL3, MATCAP1
    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
    nsv5526841copy number variation1nstd206human GRCh38 chr16: 67,175,987-67,176,137 , GRCh37.p13 chr16: 67,209,890-67,210,040 NOL3, MATCAP1
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv5005781copy number variation1nstd200human GRCh38 chr16: 67,178,586-67,199,277 , GRCh37.p13 chr16: 67,212,489-67,233,180 MATCAP1, ELMO3, 2 more genes
    nsv5005780copy number variation1nstd200human GRCh38 chr16: 67,159,261-67,221,610 , GRCh37.p13 chr16: 67,193,164-67,255,513 TRADD, HSF4, 8 more genes
    nsv5005779copy number variation1nstd200human GRCh38 chr16: 67,159,176-67,212,734 , GRCh37.p13 chr16: 67,193,079-67,246,637 EXOC3L1, FBXL9P, 8 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
    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
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