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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5947452copy number variation1nstd209human GRCh38 chr14: 77,319,170-77,332,333 , GRCh37.p13 chr14: 77,785,513-77,798,676 GSTZ1, POMT2
    nsv5939651copy number variation1nstd209human GRCh38 chr14: 77,277,923-77,278,007 , GRCh37.p13 chr14: 77,744,266-77,744,350 POMT2
    nsv5931678copy number variation1nstd209human GRCh38 chr14: 75,925,125-77,416,814 , GRCh37.p13 chr14: 76,391,468-77,883,157 TMED8, LOC105370573, 37 more genes
    nsv5850119copy number variation1nstd209human GRCh38 chr14: 77,319,027-77,323,126 , GRCh37.p13 chr14: 77,785,370-77,789,469 POMT2, GSTZ1
    nsv5709818mobile element insertion1nstd211human GRCh38 chr14: 77,304,337-77,304,337 , GRCh37.p13 chr14: 77,770,680-77,770,680 POMT2
    nsv5433063mobile element insertion1nstd206human GRCh38 chr14: 77,304,337-77,304,388 , GRCh37.p13 chr14: 77,770,680-77,770,731 POMT2
    nsv5148385mobile element insertion1nstd203human GRCh38 chr14: 77,304,319-77,304,337 , GRCh37.p13 chr14: 77,770,662-77,770,680 POMT2
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv5004821copy number variation1nstd200human GRCh38 chr14: 77,220,921-77,331,757 , GRCh37.p13 chr14: 77,687,264-77,798,100 NGB, MIR1260A, 3 more genes
    nsv5000173copy number variation1nstd200human GRCh38 chr14: 77,308,157-77,309,883 , GRCh37.p13 chr14: 77,774,500-77,776,226 POMT2
    nsv4574402mobile element insertion1nstd166human GRCh37.p13 chr14: 77,759,345-77,759,345 , GRCh38.p12 chr14: 77,293,002-77,293,002 POMT2
    nsv4529354copy number variation1nstd166human GRCh37.p13 chr14: 77,754,983-77,755,800 , GRCh38.p12 chr14: 77,288,640-77,289,457 POMT2
    nsv4501127mobile element insertion1nstd166human GRCh37.p13 chr14: 77,770,662-77,770,662 , GRCh38.p12 chr14: 77,304,319-77,304,319 POMT2
    nsv4456664copy number variation1nstd102humanPathogenic GRCh37 chr14: 77,274,990-89,803,137 , GRCh38.p12 chr14: 76,808,647-89,336,793 DYNLL1P2, GTF2A1, 126 more genes
    nsv4453689copy number variation1nstd102humanUncertain significance GRCh37 chr14: 77,743,699-78,082,942 , GRCh38 chr14: 77,277,356-77,616,599 VIPAS39, AHSA1, 9 more genes
    nsv4376851copy number variation1nstd173human GRCh37 chr14: 77,042,465-77,865,966 , GRCh38.p12 chr14: 76,576,122-77,399,623 NGB, VASH1, 29 more genes
    nsv4367285copy number variation1nstd173human GRCh37 chr14: 77,039,093-77,865,966 , GRCh38.p12 chr14: 76,572,750-77,399,623 RPSAP3, NOXRED1, 29 more genes
    nsv4221210copy number variation1nstd166human GRCh37.p13 chr14: 77,744,249-77,744,351 , GRCh38.p12 chr14: 77,277,906-77,278,008 POMT2
    nsv4217188copy number variation1nstd166human GRCh37.p13 chr14: 77,744,272-77,744,351 , GRCh38.p12 chr14: 77,277,929-77,278,008 POMT2
    nsv4214331copy number variation1nstd166human GRCh37.p13 chr14: 77,772,243-77,774,216 , GRCh38.p12 chr14: 77,305,900-77,307,873 POMT2
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