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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906746copy number variation1nstd209human GRCh38 chr4: 184,811,279-188,219,259 , GRCh37.p13 chr4: 185,732,433-189,140,413 , FLJ38576, 61 more genes
    nsv5892659copy number variation1nstd209human GRCh38 chr4: 186,546,743-186,547,283 , GRCh37.p13 chr4: 187,467,897-187,468,437 LOC105377596, MTNR1A
    nsv5890160copy number variation1nstd209human GRCh38 chr4: 186,455,504-188,157,234 , GRCh37.p13 chr4: 187,376,658-189,078,388 , LOC105377596, 27 more genes
    nsv5839086copy number variation1nstd209human GRCh38 chr4: 186,533,790-186,535,589 , GRCh37.p13 chr4: 187,454,944-187,456,743 LOC105377596, MTNR1A
    nsv5730680mobile element insertion1nstd211human GRCh38 chr4: 186,532,874-186,532,874 , GRCh37.p13 chr4: 187,454,028-187,454,028 LOC105377596, MTNR1A
    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
    nsv5642947insertion1nstd207human GRCh38 chr4: 186,540,807-186,540,807 , GRCh37.p13 chr4: 187,461,961-187,461,961 MTNR1A, LOC105377596
    nsv5642477insertion2nstd207human GRCh38 chr4: 186,547,093-186,547,093 , GRCh37.p13 chr4: 187,468,247-187,468,247 MTNR1A
    nsv5638504insertion1nstd207human GRCh38 chr4: 186,546,886-186,546,886 , GRCh37.p13 chr4: 187,468,040-187,468,040 MTNR1A
    nsv5626648insertion1nstd207human GRCh38 chr4: 186,546,790-186,546,790 , GRCh37.p13 chr4: 187,467,944-187,467,944 MTNR1A, LOC105377596
    nsv5581396copy number variation1nstd207human GRCh38 chr4: 186,546,792-186,546,894 , GRCh37.p13 chr4: 187,467,946-187,468,048 LOC105377596, MTNR1A
    nsv5576424copy number variation1nstd207human GRCh38 chr4: 186,546,654-186,546,734 , GRCh37.p13 chr4: 187,467,808-187,467,888 MTNR1A, LOC105377596
    nsv5567635copy number variation1nstd207human GRCh38 chr4: 186,547,065-186,547,122 , GRCh37.p13 chr4: 187,468,219-187,468,276 MTNR1A
    nsv5463183copy number variation1nstd206human GRCh38 chr4: 186,524,299-186,530,788 , GRCh37.p13 chr4: 187,445,453-187,451,942 LOC105377596, MTNR1A
    nsv5459728copy number variation1nstd206human GRCh38 chr4: 186,546,797-186,547,273 , GRCh37.p13 chr4: 187,467,951-187,468,427 MTNR1A, LOC105377596
    nsv5316720copy number variation1nstd204human GRCh38.p13 chr4: 186,546,844-186,547,293 , GRCh37.p13 chr4: 187,467,998-187,468,447 MTNR1A
    nsv5301181copy number variation1nstd204human GRCh38.p13 chr4: 186,407,885-186,610,947 , GRCh37.p13 chr4: 187,329,039-187,532,101 FAT1, LOC105377596, 3 more genes
    nsv5228861copy number variation1nstd204human GRCh38.p13 chr4: 186,547,101-186,547,300 , GRCh37.p13 chr4: 187,468,255-187,468,454 MTNR1A
    nsv5228440copy number variation1nstd204human GRCh38.p13 chr4: 186,407,901-186,610,900 , GRCh37.p13 chr4: 187,329,055-187,532,054 LOC105377596, FAT1, 3 more genes
    nsv5227785copy number variation1nstd204human GRCh38.p13 chr4: 186,551,039-186,552,250 , GRCh37.p13 chr4: 187,472,193-187,473,404 MTNR1A
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