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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963770insertion1nstd209human GRCh38 chr3: 157,272,060-157,272,060 , GRCh37.p13 chr3: 156,989,849-156,989,849 VEPH1, LOC101928236
    nsv5960240insertion1nstd209human GRCh38 chr3: 157,304,038-157,304,038 , GRCh37.p13 chr3: 157,021,827-157,021,827 VEPH1, LOC101928236
    nsv5952927insertion1nstd209human GRCh38 chr3: 157,305,069-157,305,069 , GRCh37.p13 chr3: 157,022,858-157,022,858 VEPH1, LOC101928236
    nsv5907009copy number variation1nstd209human GRCh38 chr3: 157,398,542-157,399,150 , GRCh37.p13 chr3: 157,116,331-157,116,939 VEPH1
    nsv5906966copy number variation1nstd209human GRCh38 chr3: 157,329,424-157,329,474 , GRCh37.p13 chr3: 157,047,213-157,047,263 VEPH1, LOC101928236
    nsv5898112copy number variation1nstd209human GRCh38 chr3: 157,379,543-157,379,712 , GRCh37.p13 chr3: 157,097,332-157,097,501 LOC101928236, VEPH1
    nsv5893420copy number variation1nstd209human GRCh38 chr3: 157,373,314-157,376,573 , GRCh37.p13 chr3: 157,091,103-157,094,362 LOC101928236, VEPH1
    nsv5835047copy number variation1nstd209human GRCh38 chr3: 157,373,277-157,376,526 , GRCh37.p13 chr3: 157,091,066-157,094,315 LOC101928236, VEPH1
    nsv5693959mobile element insertion2nstd211human GRCh38 chr3: 157,356,705-157,356,705 , GRCh37.p13 chr3: 157,074,494-157,074,494 VEPH1, LOC101928236
    nsv5691794mobile element insertion1nstd211human GRCh38 chr3: 157,406,020-157,406,020 , GRCh37.p13 chr3: 157,123,809-157,123,809 VEPH1
    nsv5687456mobile element insertion1nstd211human GRCh38 chr3: 157,277,536-157,277,536 , GRCh37.p13 chr3: 156,995,325-156,995,325 LOC101928236, VEPH1
    nsv5680290mobile element insertion1nstd211human GRCh38 chr3: 157,272,173-157,272,173 , GRCh37.p13 chr3: 156,989,962-156,989,962 VEPH1, LOC101928236
    nsv5679677mobile element insertion1nstd211human GRCh38 chr3: 157,272,276-157,272,276 , GRCh37.p13 chr3: 156,990,065-156,990,065 VEPH1, LOC101928236
    nsv5678923mobile element insertion2nstd211human GRCh38 chr3: 157,263,504-157,263,504 , GRCh37.p13 chr3: 156,981,293-156,981,293 LOC101928236, VEPH1
    nsv5675876mobile element insertion2nstd211human GRCh38 chr3: 157,369,204-157,369,204 , GRCh37.p13 chr3: 157,086,993-157,086,993 VEPH1, LOC101928236
    nsv5615970insertion1nstd207human GRCh38 chr3: 157,263,488-157,263,488 , GRCh37.p13 chr3: 156,981,277-156,981,277 LOC101928236, VEPH1
    nsv5540558insertion1nstd206human GRCh38 chr3: 157,314,906-157,314,914 , GRCh37.p13 chr3: 157,032,695-157,032,703 VEPH1, LOC101928236
    nsv5445799copy number variation1nstd206human GRCh38 chr3: 157,398,546-157,399,151 , GRCh37.p13 chr3: 157,116,335-157,116,940 VEPH1
    nsv5439467copy number variation1nstd206human GRCh38 chr3: 157,426,818-157,427,521 , GRCh37.p13 chr3: 157,144,607-157,145,310 VEPH1
    nsv5438855copy number variation1nstd206human GRCh38 chr3: 157,427,272-157,427,371 , GRCh37.p13 chr3: 157,145,061-157,145,160 VEPH1
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