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Items: 1 to 20 of 340

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116700mobile element insertion1nstd186human GRCh37 chr4: 170,588,849-170,588,900 , GRCh38.p12 chr4: 169,667,698-169,667,749 CLCN3
    nsv5960748insertion1nstd209human GRCh38 chr4: 169,667,680-169,667,680 , GRCh37.p13 chr4: 170,588,831-170,588,831 CLCN3
    nsv5691926mobile element insertion1nstd211human GRCh38 chr4: 169,687,343-169,687,343 , GRCh37.p13 chr4: 170,608,494-170,608,494 CLCN3
    nsv5690198mobile element insertion2nstd211human GRCh38 chr4: 169,667,698-169,667,698 , GRCh37.p13 chr4: 170,588,849-170,588,849 CLCN3
    nsv5637238insertion1nstd207human GRCh38 chr4: 169,667,680-169,667,680 , GRCh37.p13 chr4: 170,588,831-170,588,831 CLCN3
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5469939copy number variation1nstd206human GRCh38 chr4: 169,648,798-169,653,064 , GRCh37.p13 chr4: 170,569,949-170,574,215 CLCN3
    nsv5410500mobile element insertion1nstd206human GRCh38 chr4: 169,667,698-169,667,749 , GRCh37.p13 chr4: 170,588,849-170,588,900 CLCN3
    nsv5381776copy number variation1nstd102humanPathogenic GRCh37 chr4: 157,771,352-172,496,278 , GRCh38.p12 chr4: 156,850,200-171,575,127 LOC107986326, LOC107986240, 144 more genes
    nsv5337412translocation1nstd200human GRCh37 chr8: 84,660,338-84,660,338 , GRCh37 chr4: 170,587,315-170,587,315 , GRCh38.p12 chr8: 83,748,103-83,748,103 , GRCh38.p12 chr4: 169,666,164-169,666,164 CLCN3
    nsv5316460copy number variation1nstd204human GRCh38.p13 chr4: 169,648,773-169,653,085 , GRCh37.p13 chr4: 170,569,924-170,574,236 CLCN3
    nsv5231043copy number variation1nstd204human GRCh38.p13 chr4: 169,648,555-169,653,054 , GRCh37.p13 chr4: 170,569,706-170,574,205 CLCN3
    nsv5221718copy number variation1nstd204human GRCh38.p13 chr4: 169,648,801-169,653,000 , GRCh37.p13 chr4: 170,569,952-170,574,151 CLCN3
    nsv5099502mobile element insertion1nstd203human GRCh38 chr4: 169,667,682-169,667,698 , GRCh37.p13 chr4: 170,588,833-170,588,849 CLCN3
    nsv5099076mobile element insertion1nstd203human GRCh38 chr4: 169,667,293-169,667,312 , GRCh37.p13 chr4: 170,588,444-170,588,463 CLCN3
    nsv5098289mobile element insertion1nstd203human GRCh38 chr4: 169,667,685-169,667,698 , GRCh37.p13 chr4: 170,588,836-170,588,849 CLCN3
    nsv5096638mobile element insertion1nstd203human GRCh38 chr4: 169,667,690-169,667,698 , GRCh37.p13 chr4: 170,588,841-170,588,849 CLCN3
    nsv5094493mobile element insertion1nstd203human GRCh38 chr4: 169,667,698-169,667,721 , GRCh37.p13 chr4: 170,588,849-170,588,872 CLCN3
    nsv5092346mobile element insertion1nstd203human GRCh38 chr4: 169,667,680-169,667,698 , GRCh37.p13 chr4: 170,588,831-170,588,849 CLCN3
    nsv5086140mobile element insertion1nstd203human GRCh38 chr4: 169,667,292-169,667,312 , GRCh37.p13 chr4: 170,588,443-170,588,463 CLCN3
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