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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5973186inversion1nstd209human GRCh38 chr4: 158,500,774-158,878,861 , GRCh37.p13 chr4: 159,421,926-159,800,013 ETFDH, PPID, 4 more genes
    nsv5955165insertion1nstd209human GRCh38 chr4: 158,628,945-158,628,945 , GRCh37.p13 chr4: 159,550,097-159,550,097 RXFP1
    nsv5907174copy number variation1nstd209human GRCh38 chr4: 158,477,557-158,546,124 , GRCh37.p13 chr4: 159,398,709-159,467,276 RXFP1
    nsv5902244copy number variation1nstd209human GRCh38 chr4: 156,014,074-164,864,480 , GRCh37.p13 chr4: 156,935,226-165,785,632 , MIR3688-1, 67 more genes
    nsv5900800copy number variation1nstd209human GRCh38 chr4: 158,626,116-158,626,167 , GRCh37.p13 chr4: 159,547,268-159,547,319 RXFP1
    nsv5724841mobile element insertion1nstd211human GRCh38 chr4: 158,651,897-158,651,897 , GRCh37.p13 chr4: 159,573,049-159,573,049 RXFP1
    nsv5678116mobile element insertion2nstd211human GRCh38 chr4: 158,628,945-158,628,945 , GRCh37.p13 chr4: 159,550,097-159,550,097 RXFP1
    nsv5611220insertion1nstd207human GRCh38 chr4: 158,628,943-158,628,943 , GRCh37.p13 chr4: 159,550,095-159,550,095 RXFP1
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5550354insertion1nstd206human GRCh38 chr4: 158,628,945-158,628,957 , GRCh37.p13 chr4: 159,550,097-159,550,109 RXFP1
    nsv5538620insertion1nstd206human GRCh38 chr4: 158,626,060-158,626,112 , GRCh37.p13 chr4: 159,547,212-159,547,264 RXFP1
    nsv5534593insertion1nstd206human GRCh38 chr4: 158,567,692-158,567,742 , GRCh37.p13 chr4: 159,488,844-159,488,894 RXFP1
    nsv5468710copy number variation1nstd206human GRCh38 chr4: 158,363,000-158,611,381 , GRCh37.p13 chr4: 159,284,152-159,532,533 RXFP1, LOC105377510, 2 more genes
    nsv5466305copy number variation1nstd206human GRCh38 chr4: 158,628,204-158,628,272 , GRCh37.p13 chr4: 159,549,356-159,549,424 RXFP1
    nsv5462286copy number variation1nstd206human GRCh38 chr4: 158,608,751-158,610,181 , GRCh37.p13 chr4: 159,529,903-159,531,333 RXFP1
    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
    nsv5377801translocation1nstd200human GRCh38 chr4: 158,527,169-158,527,169 , GRCh38 chr1: 84,051,737-84,051,737 , GRCh37.p13 chr4: 159,448,321-159,448,321 , GRCh37.p13 chr1: 84,517,420-84,517,420 RXFP1
    nsv5367879translocation1nstd200human GRCh38 chr4: 158,527,166-158,527,166 , GRCh38 chr1: 84,052,267-84,052,267 , GRCh37.p13 chr1: 84,517,950-84,517,950 , GRCh37.p13 chr4: 159,448,318-159,448,318 RXFP1
    nsv5092973mobile element insertion1nstd203human GRCh38 chr4: 158,623,484-158,623,502 , GRCh37.p13 chr4: 159,544,636-159,544,654 RXFP1
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