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Items: 1 to 20 of 197

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5919795copy number variation1nstd209human GRCh38 chr7: 134,665,247-134,665,669 , GRCh37.p13 chr7: 134,349,999-134,350,421 BPGM
    nsv5574657copy number variation1nstd207human GRCh38 chr7: 134,665,247-134,665,669 , GRCh37.p13 chr7: 134,349,999-134,350,421 BPGM
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5483490copy number variation1nstd206human GRCh38 chr7: 134,665,255-134,665,670 , GRCh37.p13 chr7: 134,350,007-134,350,422 BPGM
    nsv5393906mobile element deletion1nstd186human GRCh37 chr7: 134,350,007-134,350,422 , GRCh38.p12 chr7: 134,665,255-134,665,670 BPGM
    nsv5329365mobile element deletion1nstd204human GRCh38.p13 chr7: 134,665,255-134,665,670 , GRCh37.p13 chr7: 134,350,007-134,350,422 BPGM
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5037298inversion1nstd200human GRCh38 chr7: 134,635,428-134,659,466 , GRCh37.p13 chr7: 134,320,180-134,344,218 BPGM
    nsv5035680mobile element deletion1nstd200human GRCh38 chr7: 134,665,255-134,665,670 , GRCh37.p13 chr7: 134,350,007-134,350,422 BPGM
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4968799copy number variation1nstd200human GRCh38 chr7: 134,497,770-134,660,370 , GRCh37.p13 chr7: 134,182,522-134,345,122 LOC105375520, AKR1B10, 2 more genes
    nsv4958478copy number variation1nstd200human GRCh38 chr7: 134,663,350-134,672,823 , GRCh37.p13 chr7: 134,348,102-134,357,575 BPGM
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4870254inversion1nstd200human GRCh37 chr7: 134,320,186-134,344,218 , GRCh38.p12 chr7: 134,635,434-134,659,466 BPGM
    nsv4827019copy number variation1nstd200human GRCh37 chr7: 134,350,007-134,350,422 , GRCh38.p12 chr7: 134,665,255-134,665,670 BPGM
    nsv4827018copy number variation1nstd200human GRCh37 chr7: 134,348,102-134,357,575 , GRCh38.p12 chr7: 134,663,350-134,672,823 BPGM
    nsv4745824copy number variation1nstd199human GRCh37 chr7: 134,350,003-134,350,427 , GRCh38.p12 chr7: 134,665,251-134,665,675 BPGM
    nsv4708658copy number variation4nstd195human GRCh37 chr7: 134,349,999-134,350,000 , GRCh38.p12 chr7: 134,665,247-134,665,248 BPGM
    nsv4679598copy number variation1nstd189human GRCh37.p13 chr7: 134,025,373-134,356,820 , GRCh38.p12 chr7: 134,340,621-134,672,068 AKR1B1, BPGM, 7 more genes
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 RPL26P23, ST13P17, 887 more genes
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