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Items: 1 to 20 of 242

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050278inversion1nstd229human GRCh38 chr7: 92,907,694-98,049,952 , GRCh37.p13 chr7: 92,537,008-97,679,264 LOC105375416, RNU6-364P, 88 more genes
    nsv7046393inversion1nstd229human GRCh38 chr7: 94,337,788-94,339,212 , GRCh37.p13 chr7: 93,967,100-93,968,524 LOC107986821, LOC112267858
    nsv7044141inversion1nstd229human GRCh38 chr7: 89,303,967-95,903,508 , GRCh37.p13 chr7: 88,933,281-95,532,820 MIR4652, PPP1R9A-AS1, 94 more genes
    nsv7041432inversion1nstd229human GRCh38 chr7: 94,334,402-94,338,114 , GRCh37.p13 chr7: 93,963,714-93,967,426 LOC112267858, LOC107986821
    nsv6837613copy number variation1nstd229human GRCh38 chr7: 93,459,401-94,346,300 , GRCh37.p13 chr7: 93,088,713-93,975,612 TFPI2-DT, MIR489, 14 more genes
    nsv6837192copy number variation1nstd229human GRCh38 chr7: 94,329,301-94,333,100 , GRCh37.p13 chr7: 93,958,613-93,962,412 LOC107986821, LOC112267858
    nsv6835382copy number variation1nstd229human GRCh38 chr7: 94,272,628-94,275,798 , GRCh37.p13 chr7: 93,901,940-93,905,110 LOC112267858
    nsv6832289copy number variation1nstd229human GRCh38 chr7: 94,255,598-94,279,736 , GRCh37.p13 chr7: 93,884,910-93,909,048 LOC112267858
    nsv6831795copy number variation1nstd229human GRCh38 chr7: 94,314,519-94,322,026 , GRCh37.p13 chr7: 93,943,831-93,951,338 LOC107986821, LOC112267858
    nsv6829464copy number variation1nstd229human GRCh38 chr7: 94,299,499-94,299,665 , GRCh37.p13 chr7: 93,928,811-93,928,977 LOC112267858
    nsv6828628copy number variation1nstd229human GRCh38 chr7: 94,295,616-94,343,062 , GRCh37.p13 chr7: 93,924,928-93,972,374 LOC107986821, LOC112267858
    nsv6827907copy number variation1nstd229human GRCh38 chr7: 94,352,777-94,359,696 , GRCh37.p13 chr7: 93,982,089-93,989,008 LOC112267858
    nsv6826750copy number variation1nstd229human GRCh38 chr7: 94,285,395-94,290,089 , GRCh37.p13 chr7: 93,914,707-93,919,401 LOC112267858
    nsv6823291copy number variation1nstd229human GRCh38 chr7: 94,333,259-94,338,845 , GRCh37.p13 chr7: 93,962,571-93,968,157 LOC112267858, LOC107986821
    nsv6822982copy number variation1nstd229human GRCh38 chr7: 94,329,031-94,329,332 , GRCh37.p13 chr7: 93,958,343-93,958,644 LOC107986821, LOC112267858
    nsv6821381copy number variation1nstd229human GRCh38 chr7: 94,343,666-94,347,639 , GRCh37.p13 chr7: 93,972,978-93,976,951 LOC107986821, LOC112267858
    nsv6819629copy number variation1nstd229human GRCh38 chr7: 94,222,976-94,285,328 , GRCh37.p13 chr7: 93,852,288-93,914,640 LOC112267858
    nsv6819067copy number variation1nstd229human GRCh38 chr7: 94,223,001-94,285,300 , GRCh37.p13 chr7: 93,852,313-93,914,612 LOC112267858
    nsv6818793copy number variation1nstd229human GRCh38 chr7: 94,155,701-94,354,500 , GRCh37.p13 chr7: 93,785,013-93,983,812 LOC107986821, LOC112267858
    nsv6636271copy number variation1nstd102humanPathogenic GRCh37 chr7: 92,721,627-98,311,537 , GRCh38.p12 chr7: 93,092,314-98,682,225 MARK2P10, PON2, 97 more genes
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