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Items: 1 to 20 of 225

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096805copy number variation1nstd102humanUncertain significance GRCh37 chr3: 45,435,946-49,137,751 , GRCh38.p12 chr3: 45,394,454-49,100,318 SNORA94, LIMD1-AS1, 120 more genes
    nsv6717402copy number variation1nstd229human GRCh38 chr3: 48,549,930-48,553,345 , GRCh37.p13 chr3: 48,587,363-48,590,778 PFKFB4, MIR6823
    nsv6715574copy number variation1nstd229human GRCh38 chr3: 48,548,367-48,549,088 , GRCh37.p13 chr3: 48,585,800-48,586,521 PFKFB4, MIR6823
    nsv6713770copy number variation1nstd229human GRCh38 chr3: 48,549,807-48,561,811 , GRCh37.p13 chr3: 48,587,240-48,599,244 PFKFB4, MIR6823, 1 more genes
    nsv6712813copy number variation1nstd229human GRCh38 chr3: 48,419,498-48,534,372 , GRCh37.p13 chr3: 48,460,907-48,571,805 SHISA5, PLXNB1, 6 more genes
    nsv6708120copy number variation1nstd229human GRCh38 chr3: 48,552,177-48,594,105 , GRCh37.p13 chr3: 48,589,610-48,631,538 MIR711, UCN2, 2 more genes
    nsv6700836copy number variation1nstd229human GRCh38 chr3: 48,056,801-51,204,000 , GRCh37.p13 chr3: 48,098,291-51,241,431 APEH, SLC26A6, 129 more genes
    nsv6372055copy number variation1nstd223human GRCh38 chr3: 48,386,801-49,230,000 , GRCh37.p13 chr3: 48,428,291-49,267,433 NCKIPSD, UCN2, 44 more genes
    nsv6366589copy number variation1nstd223human GRCh38 chr3: 48,534,932-48,551,285 , GRCh37.p13 chr3: 48,572,365-48,588,718 MIR6823, PFKFB4
    nsv6365587copy number variation1nstd223human GRCh38 chr3: 48,544,136-48,545,256 , GRCh37.p13 chr3: 48,581,569-48,582,689 PFKFB4
    nsv6365306copy number variation1nstd223human GRCh38 chr3: 48,429,601-48,926,800 , GRCh37.p13 chr3: 48,471,010-48,964,233 PRKAR2A-AS1, SNORA94, 25 more genes
    nsv6356858copy number variation1nstd223human GRCh38 chr3: 48,509,594-48,516,227 , GRCh37.p13 chr3: 48,547,027-48,553,660 PFKFB4
    nsv6315166copy number variation1nstd102humanPathogenic GRCh37 chr3: 44,948,482-49,115,809 , GRCh38.p12 chr3: 44,906,990-49,078,376 TMEM89, TGM4, 129 more genes
    nsv6299386copy number variation1nstd186human GRCh37 chr3: 48,585,800-48,586,517 , GRCh38.p12 chr3: 48,548,367-48,549,084 PFKFB4, MIR6823
    nsv6294481mobile element insertion1nstd186human GRCh37 chr3: 48,556,759-48,556,810 , GRCh38.p12 chr3: 48,519,326-48,519,377 PFKFB4
    nsv6253985mobile element insertion1nstd215human GRCh38 chr3: 48,524,227-48,524,227 , GRCh37.p13 chr3: 48,561,660-48,561,660 PFKFB4
    nsv6164129copy number variation1nstd214human GRCh38 chr3: 48,561,633-48,561,723 , GRCh37.p13 chr3: 48,599,066-48,599,156 UCN2, PFKFB4
    nsv6155021copy number variation1nstd214human GRCh38 chr3: 48,561,698-48,561,788 , GRCh37.p13 chr3: 48,599,131-48,599,221 UCN2, PFKFB4
    nsv6134694copy number variation1nstd213human GRCh37 chr3: 46,170,000-52,140,001 , GRCh38.p12 chr3: 46,128,508-52,105,985 ACY1, AMT, 210 more genes
    nsv6066537insertion1nstd212human GRCh38 chr3: 48,561,734-48,561,734 , GRCh37.p13 chr3: 48,599,167-48,599,167 PFKFB4, UCN2
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