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Items: 1 to 20 of 958

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098122copy number variation1nstd102humanUncertain significance GRCh37 chr7: 40,277,214-40,314,275 , GRCh38.p12 chr7: 40,237,615-40,274,676 LOC105375245, SUGCT
    nsv7098121copy number variation1nstd102humanUncertain significance GRCh37 chr7: 40,220,526-40,234,679 , GRCh38.p12 chr7: 40,180,927-40,195,080 SUGCT
    nsv7097626copy number variation1nstd102humanUncertain significance GRCh37 chr7: 40,234,618-40,277,345 , GRCh38.p12 chr7: 40,195,019-40,237,746 SUGCT
    nsv7097372copy number variation1nstd102humanUncertain significance GRCh37 chr7: 40,723,635-40,723,752 , GRCh38.p12 chr7: 40,684,036-40,684,153 SUGCT
    nsv7097371copy number variation1nstd102humanUncertain significance GRCh37 chr7: 40,085,415-40,174,739 , GRCh38.p12 chr7: 40,045,816-40,135,140 SUGCT, HIGD1AP7, 2 more genes
    nsv7054923inversion1nstd229human GRCh38 chr7: 40,599,948-40,603,445 , GRCh37.p13 chr7: 40,639,547-40,643,044 SUGCT
    nsv7052704inversion1nstd229human GRCh38 chr7: 40,265,433-40,270,829 , GRCh37.p13 chr7: 40,305,032-40,310,428 SUGCT, LOC105375245
    nsv7050601inversion1nstd229human GRCh38 chr7: 40,229,509-40,236,901 , GRCh37.p13 chr7: 40,269,108-40,276,500 SUGCT
    nsv7047222inversion1nstd229human GRCh38 chr7: 40,141,303-40,150,432 , GRCh37.p13 chr7: 40,180,902-40,190,031 THUMPD3P1, SUGCT
    nsv7046212inversion1nstd229human GRCh38 chr7: 40,839,777-40,840,871 , GRCh37.p13 chr7: 40,879,376-40,880,470 SUGCT
    nsv7045601inversion1nstd229human GRCh38 chr7: 40,339,087-40,352,828 , GRCh37.p13 chr7: 40,378,686-40,392,427 SUGCT
    nsv7043943inversion1nstd229human GRCh38 chr7: 40,308,238-40,316,753 , GRCh37.p13 chr7: 40,347,837-40,356,352 SUGCT
    nsv7043415inversion1nstd229human GRCh38 chr7: 40,549,753-40,669,841 , GRCh37.p13 chr7: 40,589,352-40,709,440 SUGCT, LOC105375244
    nsv7042379inversion1nstd229human GRCh38 chr7: 40,255,785-40,271,221 , GRCh37.p13 chr7: 40,295,384-40,310,820 SUGCT, LOC105375245
    nsv7041399inversion1nstd229human GRCh38 chr7: 40,189,628-40,215,074 , GRCh37.p13 chr7: 40,229,227-40,254,673 SUGCT
    nsv6837574copy number variation1nstd229human GRCh38 chr7: 40,082,682-40,152,007 , GRCh37.p13 chr7: 40,122,281-40,191,606 HIGD1AP7, CDK13, 3 more genes
    nsv6837542copy number variation1nstd229human GRCh38 chr7: 40,574,718-40,685,424 , GRCh37.p13 chr7: 40,614,317-40,725,023 LOC105375244, SUGCT
    nsv6837534copy number variation1nstd229human GRCh38 chr7: 40,111,401-40,157,900 , GRCh37.p13 chr7: 40,151,000-40,197,499 THUMPD3P1, HIGD1AP7, 2 more genes
    nsv6837426copy number variation1nstd229human GRCh38 chr7: 40,262,714-40,501,512 , GRCh37.p13 chr7: 40,302,313-40,541,111 LOC105375245, SUGCT
    nsv6837083copy number variation1nstd229human GRCh38 chr7: 40,330,418-40,333,575 , GRCh37.p13 chr7: 40,370,017-40,373,174 SUGCT
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