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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976512inversion1nstd209human GRCh38 chr7: 5,976,108-6,745,714 , GRCh37.p13 chr7: 6,015,739-6,785,345 PMS2, RAC1, 22 more genes
    nsv5691730mobile element insertion1nstd211human GRCh38 chr7: 6,390,096-6,390,096 , GRCh37.p13 chr7: 6,429,727-6,429,727 RAC1
    nsv5675290mobile element insertion1nstd211human GRCh38 chr7: 6,392,700-6,392,700 , GRCh37.p13 chr7: 6,432,331-6,432,331 RAC1
    nsv5667605inversion1nstd207human GRCh37.p13 chr7: 6,028,678-6,775,274 , GRCh38 chr7: 5,989,047-6,735,643 PMS2, RAC1, 22 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5554365sequence alteration1nstd206human GRCh38 chr7: 5,895,867-6,829,202 , GRCh37.p13 chr7: 5,935,498-6,868,833 , RAC1, 28 more genes
    nsv5551221insertion1nstd206human GRCh38 chr7: 6,375,786-6,375,823 , GRCh37.p13 chr7: 6,415,417-6,415,454 RAC1
    nsv5541651insertion1nstd206human GRCh38 chr7: 6,374,453-6,374,464 , GRCh37.p13 chr7: 6,414,084-6,414,095 RAC1
    nsv5396506mobile element insertion1nstd206human GRCh38 chr7: 6,392,700-6,392,751 , GRCh37.p13 chr7: 6,432,331-6,432,382 RAC1
    nsv5238742copy number variation1nstd204human GRCh38.p13 chr7: 6,376,701-6,446,400 , GRCh37.p13 chr7: 6,416,332-6,486,031 RAC1, DAGLB
    nsv5232182copy number variation1nstd204human GRCh38.p13 chr7: 6,198,401-6,448,100 , GRCh37.p13 chr7: 6,238,032-6,487,731 RAC1, CYTH3, 3 more genes
    nsv5232028copy number variation1nstd204human GRCh38.p13 chr7: 6,381,489-6,386,788 , GRCh37.p13 chr7: 6,421,120-6,426,419 RAC1
    nsv5229919copy number variation1nstd204human GRCh38.p13 chr7: 6,314,201-6,774,600 , GRCh37.p13 chr7: 6,353,832-6,814,231 GRID2IP, PMS2CL, 14 more genes
    nsv5113308mobile element insertion1nstd203human GRCh38 chr7: 6,392,682-6,392,700 , GRCh37.p13 chr7: 6,432,313-6,432,331 RAC1
    nsv5101549mobile element insertion1nstd203human GRCh38 chr7: 6,375,772-6,375,785 , GRCh37.p13 chr7: 6,415,403-6,415,416 RAC1
    nsv4953311copy number variation1nstd200human GRCh38 chr7: 6,381,620-6,406,734 , GRCh37.p13 chr7: 6,421,251-6,446,365 RAC1
    nsv4953310copy number variation1nstd200human GRCh38 chr7: 6,379,607-6,384,110 , GRCh37.p13 chr7: 6,419,238-6,423,741 RAC1
    nsv4953307copy number variation1nstd200human GRCh38 chr7: 6,207,809-6,651,290 , GRCh37.p13 chr7: 6,247,440-6,690,921 ZNF853, DAGLB, 11 more genes
    nsv4950006copy number variation1nstd200human GRCh38 chr7: 6,393,359-6,397,961 , GRCh37.p13 chr7: 6,432,990-6,437,592 RAC1
    nsv4950005copy number variation1nstd200human GRCh38 chr7: 6,381,488-6,383,870 , GRCh37.p13 chr7: 6,421,119-6,423,501 RAC1
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