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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072039inversion1nstd229human GRCh38 chr16: 79,903,600-82,537,648 , GRCh37.p13 chr16: 79,937,497-82,571,253 RN7SKP176, LOC105371357, 34 more genes
    nsv7070808inversion1nstd229human GRCh38 chr16: 79,903,594-82,532,651 , GRCh37.p13 chr16: 79,937,491-82,566,256 DYNLRB2, RNU6-1191P, 34 more genes
    nsv6995939copy number variation1nstd229human GRCh38 chr16: 81,542,755-81,935,940 , GRCh37.p13 chr16: 81,576,360-81,969,545 MIR6504, LOC105371362, 3 more genes
    nsv6994608copy number variation1nstd229human GRCh38 chr16: 76,392,054-84,158,971 , GRCh37.p13 chr16: 76,425,951-84,192,576 , MAFTRR, 87 more genes
    nsv6989574copy number variation1nstd229human GRCh38 chr16: 81,358,074-81,706,386 , GRCh37.p13 chr16: 81,391,679-81,739,991 MIR4720, LOC105371362, 6 more genes
    nsv6984896copy number variation1nstd229human GRCh38 chr16: 80,642,208-81,673,247 , GRCh37.p13 chr16: 80,676,105-81,706,852 RNU6-1191P, BCO1, 18 more genes
    nsv6983976copy number variation1nstd229human GRCh38 chr16: 80,966,228-81,785,439 , GRCh37.p13 chr16: 81,000,125-81,819,044 PLCG2, PPIAP51, 17 more genes
    nsv6981137copy number variation1nstd229human GRCh38 chr16: 81,608,253-81,618,802 , GRCh37.p13 chr16: 81,641,858-81,652,407 CMIP, MIR6504
    nsv6634465copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 71,610,276-90,354,753 , GRCh38.p12 chr16: 71,576,373-90,228,345 AP1G1, AFG3L1P, 349 more genes
    nsv6623777copy number variation1nstd224human GRCh37 chr16: 81,429,758-81,694,850 , GRCh38.p12 chr16: 81,396,153-81,661,245 MIR7854, LOC105371362, 3 more genes
    nsv6576763inversion1nstd223human GRCh38 chr16: 81,262,059-82,043,442 , GRCh37.p13 chr16: 81,295,664-82,077,047 LOC112268169, LOC105371362, 13 more genes
    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
    nsv6290331copy number variation1nstd102humanPathogenic GRCh37 chr16: 80,386,595-90,163,348 , GRCh38.p12 chr16: 80,352,698-90,096,940 GINS2, TCF25, 220 more genes
    nsv6133210copy number variation1nstd213human GRCh37 chr16: 78,970,000-88,180,001 , GRCh38.p12 chr16: 78,936,103-88,146,395 , CA5A, 152 more genes
    nsv6133206copy number variation1nstd213human GRCh37 chr16: 74,460,000-84,740,001 , GRCh38.p12 chr16: 74,426,102-84,706,395 , CDH13, 142 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
    nsv5522915copy number variation1nstd206human GRCh38 chr16: 81,369,621-81,867,737 , GRCh37.p13 chr16: 81,403,226-81,901,342 PLCG2, GAN, 7 more genes
    nsv4866898copy number variation1nstd200human GRCh37 chr16: 81,645,029-81,645,808 , GRCh38.p12 chr16: 81,611,424-81,612,203 CMIP, MIR6504
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729841copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 80,483,625-82,044,152 , GRCh38.p12 chr16: 80,449,728-82,010,547 GCSH, PLCG2, 25 more genes
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