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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137701copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 28,669,064-31,367,407 , GRCh38.p12 chr13: 28,094,927-30,793,270 ALOX5AP, FLT1, 41 more genes
    nsv6112810copy number variation1nstd102humanPathogenic GRCh37 chr13: 28,925,153-34,061,696 , GRCh38.p12 chr13: 28,351,016-33,487,559 MTUS2, ALOX5AP, 70 more genes
    nsv5930083copy number variation1nstd209human GRCh38 chr13: 30,622,821-30,623,631 , GRCh37.p13 chr13: 31,196,958-31,197,768 USPL1
    nsv5929234copy number variation1nstd209human GRCh38 chr13: 30,619,632-30,619,896 , GRCh37.p13 chr13: 31,193,769-31,194,033 USPL1
    nsv5594294copy number variation1nstd207human GRCh38 chr13: 30,637,916-30,640,863 , GRCh37.p13 chr13: 31,212,053-31,215,000 USPL1
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5509123copy number variation1nstd206human GRCh38 chr13: 30,619,638-30,619,897 , GRCh37.p13 chr13: 31,193,775-31,194,034 USPL1
    nsv5502756copy number variation1nstd206human GRCh38 chr13: 30,626,805-30,626,922 , GRCh37.p13 chr13: 31,200,942-31,201,059 USPL1
    nsv5499878copy number variation1nstd206human GRCh38 chr13: 30,622,821-30,623,633 , GRCh37.p13 chr13: 31,196,958-31,197,770 USPL1
    nsv5499856copy number variation1nstd206human GRCh38 chr13: 30,643,765-30,643,874 , GRCh37.p13 chr13: 31,217,902-31,218,011 USPL1
    nsv5499787copy number variation1nstd206human GRCh38 chr13: 30,637,971-30,640,992 , GRCh37.p13 chr13: 31,212,108-31,215,129 USPL1
    nsv5356734translocation1nstd200human GRCh38 chr13: 30,622,821-30,622,821 , GRCh38 chr13: 30,623,633-30,623,633 , GRCh37.p13 chr13: 31,197,770-31,197,770 , GRCh37.p13 chr13: 31,196,958-31,196,958 USPL1
    nsv5335676translocation1nstd200human GRCh37 chr13: 31,196,958-31,196,958 , GRCh37 chr13: 31,197,770-31,197,770 , GRCh38.p12 chr13: 30,622,821-30,622,821 , GRCh38.p12 chr13: 30,623,633-30,623,633 USPL1
    nsv5326591translocation1nstd204human GRCh38.p13 chr13: 30,623,633-30,623,633 , GRCh38.p13 chr13: 30,622,821-30,622,821 , GRCh37.p13 chr13: 31,196,958-31,196,958 , GRCh37.p13 chr13: 31,197,770-31,197,770 USPL1
    nsv5301118copy number variation1nstd204human GRCh38.p13 chr13: 30,637,982-30,640,946 , GRCh37.p13 chr13: 31,212,119-31,215,083 USPL1
    nsv5272305copy number variation1nstd204human GRCh38.p13 chr13: 30,637,927-30,641,072 , GRCh37.p13 chr13: 31,212,064-31,215,209 USPL1
    nsv5268210copy number variation1nstd204human GRCh38.p13 chr13: 30,638,001-30,641,100 , GRCh37.p13 chr13: 31,212,138-31,215,237 USPL1
    nsv5151349mobile element insertion1nstd203human GRCh38 chr13: 30,648,454-30,648,469 , GRCh37.p13 chr13: 31,222,591-31,222,606 USPL1
    nsv5004450copy number variation1nstd200human GRCh38 chr13: 30,638,086-30,641,231 , GRCh37.p13 chr13: 31,212,223-31,215,368 USPL1
    nsv4996791copy number variation1nstd200human GRCh38 chr13: 30,619,638-30,619,897 , GRCh37.p13 chr13: 31,193,775-31,194,034 USPL1
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