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Items: 1 to 20 of 140

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5530711copy number variation1nstd206human GRCh38 chr20: 8,020,900-8,022,844 , GRCh37.p13 chr20: 8,001,547-8,003,491 TMX4-AS1
    nsv5012436copy number variation1nstd200human GRCh38 chr20: 8,020,900-8,022,844 , GRCh37.p13 chr20: 8,001,547-8,003,491 TMX4-AS1
    nsv5012435copy number variation1nstd200human GRCh38 chr20: 8,020,895-8,021,842 , GRCh37.p13 chr20: 8,001,542-8,002,489 TMX4-AS1
    nsv4861854copy number variation1nstd200human GRCh37 chr20: 8,001,542-8,002,489 , GRCh38.p12 chr20: 8,020,895-8,021,842 TMX4-AS1
    nsv4738938copy number variation1nstd199human GRCh37 chr20: 7,998,956-7,999,108 , GRCh38.p12 chr20: 8,018,309-8,018,461 TMX4, TMX4-AS1
    nsv4676293copy number variation1nstd102humanLikely benign GRCh37 chr20: 7,374,347-8,111,284 , GRCh38.p12 chr20: 7,393,700-8,130,637 PLCB1, SRSF10P2, 6 more genes
    nsv4676182copy number variation1nstd102humanUncertain significance GRCh37 chr20: 7,052,456-8,140,338 , GRCh38.p12 chr20: 7,071,809-8,159,691 RN7SL547P, MIR8062, 10 more genes
    nsv4666770copy number variation1nstd186human GRCh37 chr20: 8,001,544-8,003,491 , GRCh38.p12 chr20: 8,020,897-8,022,844 TMX4-AS1
    nsv4623032copy number variation1nstd183human GRCh37 chr20: 8,001,544-8,003,491 , GRCh38.p12 chr20: 8,020,897-8,022,844 TMX4-AS1
    nsv4621743copy number variation1nstd183human GRCh37 chr20: 7,102,847-8,575,576 , GRCh38.p12 chr20: 7,122,200-8,594,929 LINC01428, PLCB1-IT1, 11 more genes
    nsv4620981copy number variation1nstd183human GRCh37 chr20: 7,548,252-8,317,079 , GRCh38.p12 chr20: 7,567,605-8,336,432 PHKBP1, PLCB1, 7 more genes
    nsv4505940mobile element insertion1nstd166human GRCh37.p13 chr20: 7,998,264-7,998,264 , GRCh38.p12 chr20: 8,017,617-8,017,617 TMX4, TMX4-AS1
    nsv4457862copy number variation1nstd102humanUncertain significance GRCh37 chr20: 7,548,348-8,317,079 , GRCh38.p12 chr20: 7,567,701-8,336,432 PLCB1, PLCB1-IT1, 7 more genes
    nsv4457784copy number variation1nstd102humanUncertain significance GRCh37 chr20: 7,106,288-8,572,965 , GRCh38.p12 chr20: 7,125,641-8,592,318 PHKBP1, SRSF10P2, 11 more genes
    nsv4457490copy number variation1nstd102humanUncertain significance GRCh37 chr20: 7,092,284-8,586,513 , GRCh38.p12 chr20: 7,111,637-8,605,866 LOC105372518, TMX4, 11 more genes
    nsv4457377copy number variation1nstd102humanUncertain significance GRCh37 chr20: 7,106,057-8,572,824 , GRCh38.p12 chr20: 7,125,410-8,592,177 TMX4, HAO1, 11 more genes
    nsv4429346copy number variation1nstd174human GRCh37 chr20: 8,001,544-8,003,521 , GRCh38.p12 chr20: 8,020,897-8,022,874 TMX4-AS1
    nsv4387122copy number variation1nstd173human GRCh37 chr20: 7,092,360-8,089,968 , GRCh38.p12 chr20: 7,111,713-8,109,321 TMX4-AS1, PHKBP1, 9 more genes
    nsv4378697copy number variation1nstd173human GRCh37 chr20: 7,106,058-8,089,968 , GRCh38.p12 chr20: 7,125,411-8,109,321 LINC01706, HAO1, 9 more genes
    nsv4366268copy number variation1nstd173human GRCh37 chr20: 7,085,937-8,571,827 , GRCh38.p12 chr20: 7,105,290-8,591,180 LINC01751, PLCB1-IT1, 11 more genes
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