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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968909inversion1nstd209human GRCh38 chr4: 184,990,077-186,324,974 , GRCh37.p13 chr4: 185,911,231-187,246,128 SLC25A4, F11, 25 more genes
    nsv5906746copy number variation1nstd209human GRCh38 chr4: 184,811,279-188,219,259 , GRCh37.p13 chr4: 185,732,433-189,140,413 , FLJ38576, 61 more genes
    nsv5903072copy number variation1nstd209human GRCh38 chr4: 186,008,703-186,213,064 , GRCh37.p13 chr4: 186,929,857-187,134,218 TLR3, FAM149A, 5 more genes
    nsv5894987copy number variation1nstd209human GRCh38 chr4: 186,198,574-186,198,632 , GRCh37.p13 chr4: 187,119,728-187,119,786 CYP4V2
    nsv5889415copy number variation1nstd209human GRCh38 chr4: 186,208,119-186,208,185 , GRCh37.p13 chr4: 187,129,273-187,129,339 CYP4V2
    nsv5839081copy number variation1nstd209human GRCh38 chr4: 186,206,835-186,239,355 , GRCh37.p13 chr4: 187,127,989-187,160,509 KLKB1, CYP4V2
    nsv5839080copy number variation1nstd209human GRCh38 chr4: 186,176,909-186,194,470 , GRCh37.p13 chr4: 187,098,063-187,115,624 FLJ38576, CYP4V2
    nsv5838220copy number variation1nstd209human GRCh38 chr4: 186,212,435-186,214,234 , GRCh37.p13 chr4: 187,133,589-187,135,388 KLKB1, CYP4V2
    nsv5673650copy number variation1nstd102humanPathogenic GRCh37 chr4: 186,997,774-187,630,981 , GRCh38.p12 chr4: 186,076,620-186,709,827 FLJ38576, SLC25A5P6, 13 more genes
    nsv5640365insertion1nstd207human GRCh38 chr4: 186,204,418-186,204,418 , GRCh37.p13 chr4: 187,125,572-187,125,572 CYP4V2
    nsv5564191copy number variation1nstd102humanUncertain significance GRCh37 chr4: 187,112,978-187,131,795 , GRCh38.p12 chr4: 186,191,824-186,210,641 CYP4V2, FLJ38576
    nsv5469253copy number variation1nstd206human GRCh38 chr4: 186,198,577-186,198,633 , GRCh37.p13 chr4: 187,119,731-187,119,787 CYP4V2
    nsv5465286copy number variation1nstd206human GRCh38 chr4: 186,211,918-186,223,979 , GRCh37.p13 chr4: 187,133,072-187,145,133 KLKB1, CYP4V2
    nsv5307443copy number variation1nstd204human GRCh38.p13 chr4: 185,946,317-186,402,737 , GRCh37.p13 chr4: 186,867,471-187,323,891 LTO1P1, RPSAP70, 10 more genes
    nsv5233609copy number variation1nstd204human GRCh38.p13 chr4: 186,176,709-186,221,465 , GRCh37.p13 chr4: 187,097,863-187,142,619 KLKB1, CYP4V2, 1 more genes
    nsv5227796copy number variation1nstd204human GRCh38.p13 chr4: 186,177,101-186,292,100 , GRCh37.p13 chr4: 187,098,255-187,213,254 CYP4V2, F11, 3 more genes
    nsv5226122copy number variation1nstd204human GRCh38.p13 chr4: 186,177,043-186,217,865 , GRCh37.p13 chr4: 187,098,197-187,139,019 CYP4V2, FLJ38576, 1 more genes
    nsv5226062copy number variation1nstd204human GRCh38.p13 chr4: 186,187,298-186,189,570 , GRCh37.p13 chr4: 187,108,452-187,110,724 CYP4V2, FLJ38576
    nsv5200366copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 179,554,876-190,916,678 , GRCh38.p12 chr4: 178,633,722-189,995,523 SLC25A4, CASP3, 151 more genes
    nsv5034969inversion1nstd200human GRCh38 chr4: 185,525,494-188,054,826 , GRCh37.p13 chr4: 186,446,648-188,975,980 , F11-AS1, 34 more genes
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