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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146777copy number variation1nstd232human GRCh37.p13 chr16: 86,370,337-86,370,391 , GRCh38.p12 chr16: 86,336,731-86,336,785 LINC00917
    nsv7094605copy number variation1nstd102humanUncertain significance GRCh37 chr16: 85,936,622-86,602,447 , GRCh38.p12 chr16: 85,903,016-86,568,841 LINC00917, RPL7AP63, 16 more genes
    nsv6996222copy number variation1nstd229human GRCh38 chr16: 86,324,301-86,588,300 , GRCh37.p13 chr16: 86,357,907-86,621,906 FOXF1, FENDRR, 8 more genes
    nsv6981943copy number variation1nstd229human GRCh38 chr16: 86,336,528-86,433,745 , GRCh37.p13 chr16: 86,370,134-86,467,351 LINC00917, LOC401864
    nsv6979502copy number variation1nstd229human GRCh38 chr16: 86,345,730-86,348,684 , GRCh37.p13 chr16: 86,379,336-86,382,290 LINC00917
    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
    nsv6623942copy number variation1nstd224human GRCh37 chr16: 86,290,512-86,710,660 , GRCh38.p12 chr16: 86,256,906-86,677,054 LINC02135, FENDRR, 10 more genes
    nsv6623790copy number variation1nstd224human GRCh37 chr16: 86,189,977-87,237,863 , GRCh38.p12 chr16: 86,156,371-87,204,257 FOXC2, FENDRR, 17 more genes
    nsv6499069copy number variation1nstd223human GRCh38 chr16: 86,336,528-86,433,745 , GRCh37.p13 chr16: 86,370,134-86,467,351 LINC00917, LOC401864
    nsv6315588copy number variation1nstd222human GRCh37.p13 chr16: 85,986,306-86,727,693 , GRCh38 chr16: 85,952,700-86,694,087 FOXF1, FOXL1, 13 more genes
    nsv6314986copy number variation1nstd102humanPathogenic GRCh37 chr16: 86,225,081-86,590,510 , GRCh38.p12 chr16: 86,191,475-86,556,904 LINC01081, LINC01082, 8 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
    nsv6289897copy number variation1nstd102humanPathogenic GRCh37 chr16: 86,243,180-87,703,229 , GRCh38.p12 chr16: 86,209,574-87,669,623 LINC02135, FOXF1, 28 more genes
    nsv6274038copy number variation1nstd214human GRCh38 chr16: 86,336,810-86,336,929 , GRCh37.p13 chr16: 86,370,416-86,370,535 LINC00917
    nsv6272557copy number variation1nstd214human GRCh38 chr16: 86,336,734-86,336,792 , GRCh37.p13 chr16: 86,370,340-86,370,398 LINC00917
    nsv6207469copy number variation1nstd214human GRCh38 chr16: 86,337,978-86,338,036 , GRCh37.p13 chr16: 86,371,584-86,371,642 LINC00917
    nsv6204993copy number variation1nstd214human GRCh38 chr16: 86,337,933-86,338,024 , GRCh37.p13 chr16: 86,371,539-86,371,630 LINC00917
    nsv6194918copy number variation1nstd214human GRCh38 chr16: 86,337,084-86,337,143 , GRCh37.p13 chr16: 86,370,690-86,370,749 LINC00917
    nsv6192778copy number variation1nstd214human GRCh38 chr16: 86,338,056-86,338,118 , GRCh37.p13 chr16: 86,371,662-86,371,724 LINC00917
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