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Items: 1 to 20 of 304

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979093inversion1nstd209human GRCh38 chr7: 150,023,235-154,074,108 , GRCh37.p13 chr7: 149,720,324-153,771,193 , AOC1, 98 more genes
    nsv5925410copy number variation1nstd209human GRCh38 chr7: 154,058,973-154,059,052 , GRCh37.p13 chr7: 153,756,058-153,756,137 , DPP6, 1 more genes
    nsv5925249copy number variation1nstd209human GRCh38 chr7: 154,059,022-154,062,596 , GRCh37.p13 chr7: 153,756,107-153,759,681 , DPP6, 1 more genes
    nsv5922914copy number variation1nstd209human GRCh38 chr7: 154,059,192-154,060,877 , GRCh37.p13 chr7: 153,756,277-153,757,962 , DPP6, 1 more genes
    nsv5921530copy number variation1nstd209human GRCh38 chr7: 154,060,351-154,062,593 , GRCh37.p13 chr7: 153,757,436-153,759,678 , DPP6, 1 more genes
    nsv5916739copy number variation1nstd209human GRCh38 chr7: 154,060,357-154,083,561 , GRCh37.p13 chr7: 153,757,442-153,780,646 , DPP6, 1 more genes
    nsv5913927copy number variation1nstd209human GRCh38 chr7: 154,057,282-154,060,745 , GRCh37.p13 chr7: 153,754,367-153,757,830 , DPP6, 1 more genes
    nsv5913602copy number variation1nstd209human GRCh38 chr7: 154,060,711-154,062,775 , GRCh37.p13 chr7: 153,757,796-153,759,860 , DPP6, 1 more genes
    nsv5847802copy number variation1nstd209human GRCh38 chr7: 154,049,896-154,059,004 , GRCh37.p13 chr7: 153,746,981-153,756,089 , LOC101929998, 1 more genes
    nsv5642785insertion1nstd207human GRCh38 chr7: 154,060,346-154,060,346 , GRCh37.p13 chr7: 153,757,431-153,757,431 , DPP6, 1 more genes
    nsv5640509insertion1nstd207human GRCh38 chr7: 154,060,794-154,060,794 , GRCh37.p13 chr7: 153,757,879-153,757,879 , DPP6, 1 more genes
    nsv5632276insertion1nstd207human GRCh38 chr7: 154,059,002-154,059,002 , GRCh37.p13 chr7: 153,756,087-153,756,087 , DPP6, 1 more genes
    nsv5630271insertion1nstd207human GRCh38 chr7: 154,059,846-154,059,846 , GRCh37.p13 chr7: 153,756,931-153,756,931 , DPP6, 1 more genes
    nsv5629070insertion1nstd207human GRCh38 chr7: 154,060,744-154,060,744 , GRCh37.p13 chr7: 153,757,829-153,757,829 , DPP6, 1 more genes
    nsv5578619copy number variation1nstd207human GRCh38 chr7: 154,060,314-154,060,702 , GRCh37.p13 chr7: 153,757,399-153,757,787 , DPP6, 1 more genes
    nsv5574252copy number variation1nstd207human GRCh38 chr7: 154,059,963-154,060,824 , GRCh37.p13 chr7: 153,757,048-153,757,909 , DPP6, 1 more genes
    nsv5571687copy number variation1nstd207human GRCh38 chr7: 154,058,406-154,058,567 , GRCh37.p13 chr7: 153,755,491-153,755,652 , DPP6, 1 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
    nsv5493876copy number variation1nstd206human GRCh38 chr7: 154,058,295-154,059,085 , GRCh37.p13 chr7: 153,755,380-153,756,170 , DPP6, 1 more genes
    nsv5477608copy number variation1nstd206human GRCh38 chr7: 154,058,237-154,058,410 , GRCh37.p13 chr7: 153,755,322-153,755,495 , LOC101929998, 1 more genes
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