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Items: 1 to 20 of 114

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112768copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,984,696-46,405,042 , GRCh38.p12 chr5: 34,984,591-46,404,940 LIFR-AS1, FGF10-AS1, 137 more genes
    nsv5899458copy number variation1nstd209human GRCh38 chr5: 42,984,841-42,984,933 , GRCh37.p13 chr5: 42,984,943-42,985,035 FLJ32255
    nsv5893425copy number variation1nstd209human GRCh38 chr5: 42,962,141-43,046,337 , GRCh37.p13 chr5: 42,962,243-43,046,439 ANXA2R-AS1, ANXA2R, 6 more genes
    nsv5842991copy number variation2nstd209human GRCh38 chr5: 42,983,556-42,984,855 , GRCh37.p13 chr5: 42,983,658-42,984,957 FLJ32255
    nsv5472401copy number variation1nstd206human GRCh38 chr5: 42,981,274-43,020,548 , GRCh37.p13 chr5: 42,981,376-43,020,650 LOC105374748, ANXA2R-OT1, 2 more genes
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5381781copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,081,195-45,294,031 , GRCh38.p12 chr5: 29,081,088-45,293,929 ST3GAL5P1, LOC105374711, 213 more genes
    nsv5314322copy number variation1nstd204human GRCh38.p13 chr5: 42,481,979-42,986,910 , GRCh37.p13 chr5: 42,482,081-42,987,012 PPIAP77, SELENOP, 8 more genes
    nsv5238641copy number variation1nstd204human GRCh38.p13 chr5: 42,993,701-43,022,300 , GRCh37.p13 chr5: 42,993,803-43,022,402 ANXA2R-OT1, FLJ32255, 2 more genes
    nsv5222854copy number variation1nstd204human GRCh38.p13 chr5: 42,982,101-42,986,900 , GRCh37.p13 chr5: 42,982,203-42,987,002 FLJ32255
    nsv5221254copy number variation1nstd204human GRCh37.p13 chr5: 42,983,603-43,087,202 , GRCh38.p13 chr5: 42,983,501-43,087,100 ANXA2R-AS1, ANXA2R, 6 more genes
    nsv4946875copy number variation1nstd200human GRCh38 chr5: 42,935,801-43,057,179 , GRCh37.p13 chr5: 42,935,903-43,057,281 ANXA2R-AS1, ANXA2R, 6 more genes
    nsv4944643copy number variation1nstd200human GRCh38 chr5: 42,854,660-43,095,722 , GRCh37.p13 chr5: 42,854,762-43,095,824 LOC100132356, LOC100506639, 12 more genes
    nsv4805416copy number variation1nstd200human GRCh37 chr5: 42,482,090-42,987,004 , GRCh38.p12 chr5: 42,481,988-42,986,902 CCDC152, PRELID3BP7, 8 more genes
    nsv4674231copy number variation1nstd102humanPathogenic GRCh37 chr5: 38,432,180-49,441,945 , GRCh38.p12 chr5: 38,432,078-50,146,111 RPSAP38, LOC105374746, 92 more genes
    nsv4456866copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,453,883-46,389,339 , GRCh38.p12 chr5: 34,453,778-46,389,237 LOC100506639, EEF1A1P19, 146 more genes
    nsv4455333copy number variation1nstd102humanUncertain significance GRCh37 chr5: 42,802,309-43,040,495 , GRCh38.p12 chr5: 42,802,207-43,040,393 ANXA2R-AS1, LOC105374745, 12 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4322917inversion1nstd166human GRCh37.p13 chr5: 37,539,888-43,176,744 , GRCh38.p12 chr5: 37,539,786-43,176,642 , PTGER4, 86 more genes
    nsv4128584copy number variation1nstd166human GRCh37.p13 chr5: 42,982,000-43,020,500 , GRCh38.p12 chr5: 42,981,898-43,020,398 FLJ32255, LOC105374748, 2 more genes
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