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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096974copy number variation1nstd102humanUncertain significance GRCh37 chr4: 121,616,266-124,323,706 , GRCh38.p12 chr4: 120,695,111-123,402,551 RN7SL335P, QRFPR, 40 more genes
    nsv7046858inversion1nstd229human GRCh38 chr4: 120,026,051-121,477,397 , GRCh37.p13 chr4: 120,947,206-122,398,552 RN7SKP137, LOC107986309, 14 more genes
    nsv7043432inversion1nstd229human GRCh38 chr4: 117,041,189-125,064,058 , GRCh37.p13 chr4: 117,962,345-125,985,213 SEPTIN14P4, LINC02516, 109 more genes
    nsv6753186copy number variation1nstd229human GRCh38 chr4: 121,029,564-121,117,239 , GRCh37.p13 chr4: 121,950,719-122,038,394 RN7SKP137, NDNF-AS1, 1 more genes
    nsv6751119copy number variation1nstd229human GRCh38 chr4: 121,055,496-121,055,648 , GRCh37.p13 chr4: 121,976,651-121,976,803 NDNF
    nsv6748674copy number variation1nstd229human GRCh38 chr4: 121,023,028-121,034,700 , GRCh37.p13 chr4: 121,944,183-121,955,855 NDNF
    nsv6744962copy number variation1nstd229human GRCh38 chr4: 121,026,197-121,030,993 , GRCh37.p13 chr4: 121,947,352-121,952,148 NDNF
    nsv6570561inversion1nstd223human GRCh38 chr4: 117,041,188-125,064,052 , GRCh37.p13 chr4: 117,962,344-125,985,207 MYOZ2, NT5C3AP1, 109 more genes
    nsv6565461inversion1nstd223human GRCh38 chr4: 121,065,265-121,065,568 , GRCh37.p13 chr4: 121,986,420-121,986,723 NDNF
    nsv6387350copy number variation1nstd223human GRCh38 chr4: 121,041,425-121,042,139 , GRCh37.p13 chr4: 121,962,580-121,963,294 NDNF
    nsv6387022copy number variation1nstd223human GRCh38 chr4: 121,055,496-121,055,648 , GRCh37.p13 chr4: 121,976,651-121,976,803 NDNF
    nsv6383756copy number variation1nstd223human GRCh38 chr4: 121,063,536-121,064,017 , GRCh37.p13 chr4: 121,984,691-121,985,172 NDNF
    nsv6380198copy number variation1nstd223human GRCh38 chr4: 120,985,648-121,315,408 , GRCh37.p13 chr4: 121,906,803-122,236,563 TNIP3, NDNF, 3 more genes
    nsv6313878copy number variation1nstd102humanPathogenic GRCh37 chr4: 104,715,235-145,252,595 , GRCh38.p12 chr4: 103,794,078-144,331,443 LINC00613, GYPA, 448 more genes
    nsv6313750copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,888,785-129,649,979 , GRCh38.p12 chr4: 115,967,629-128,728,824 LOC105377395, SEPTIN7P14, 152 more genes
    nsv6297982copy number variation1nstd186human GRCh37 chr4: 121,981,582-121,981,658 , GRCh38.p12 chr4: 121,060,427-121,060,503 RN7SKP137, NDNF
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6290265copy number variation1nstd102humanPathogenic GRCh37 chr4: 114,872,547-138,005,267 , GRCh38.p12 chr4: 113,951,391-137,084,113 LOC105379404, IL21-AS1, 218 more genes
    nsv6255246mobile element insertion1nstd215human GRCh38 chr4: 121,063,024-121,063,024 , GRCh37.p13 chr4: 121,984,179-121,984,179 NDNF
    nsv6161984copy number variation1nstd214human GRCh38 chr4: 121,069,088-121,069,166 , GRCh37.p13 chr4: 121,990,243-121,990,321 NDNF
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