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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129266insertion1nstd186human GRCh37 chr20: 50,024,987-50,024,987 , GRCh38.p12 chr20: 51,408,450-51,408,450 NFATC2
    nsv5969500insertion1nstd209human GRCh38 chr20: 51,540,657-51,540,657 , GRCh37.p13 chr20: 50,157,196-50,157,196 NFATC2
    nsv5960207copy number variation1nstd209human GRCh38 chr20: 51,397,033-51,397,136 , GRCh37.p13 chr20: 50,013,570-50,013,673 NFATC2, LOC105372663
    nsv5957666copy number variation1nstd209human GRCh38 chr20: 51,519,567-51,520,270 , GRCh37.p13 chr20: 50,136,106-50,136,809 NFATC2
    nsv5955959copy number variation1nstd209human GRCh38 chr20: 51,422,956-51,423,036 , GRCh37.p13 chr20: 50,039,493-50,039,573 NFATC2
    nsv5955774copy number variation1nstd209human GRCh38 chr20: 51,434,173-51,434,236 , GRCh37.p13 chr20: 50,050,710-50,050,773 NFATC2
    nsv5952326copy number variation1nstd209human GRCh38 chr20: 51,395,307-51,395,360 , GRCh37.p13 chr20: 50,011,844-50,011,897 LOC105372663, NFATC2
    nsv5721526mobile element insertion2nstd211human GRCh38 chr20: 51,559,879-51,559,879 , GRCh37.p13 chr20: 50,176,418-50,176,418 NFATC2
    nsv5709509mobile element insertion2nstd211human GRCh38 chr20: 51,429,758-51,429,758 , GRCh37.p13 chr20: 50,046,295-50,046,295 NFATC2
    nsv5670453insertion1nstd207human GRCh38 chr20: 51,500,818-51,500,818 , GRCh37.p13 chr20: 50,117,357-50,117,357 NFATC2
    nsv5669856insertion1nstd207human GRCh38 chr20: 51,408,450-51,408,450 , GRCh37.p13 chr20: 50,024,987-50,024,987 NFATC2
    nsv5593027copy number variation1nstd207human GRCh38 chr20: 51,434,173-51,434,236 , GRCh37.p13 chr20: 50,050,710-50,050,773 NFATC2
    nsv5546946insertion1nstd206human GRCh38 chr20: 51,408,450-51,408,450 , GRCh37.p13 chr20: 50,024,987-50,024,987 NFATC2
    nsv5528741copy number variation1nstd206human GRCh38 chr20: 51,395,307-51,395,362 , GRCh37.p13 chr20: 50,011,844-50,011,899 NFATC2, LOC105372663
    nsv5526132copy number variation1nstd206human GRCh38 chr20: 51,477,325-51,482,915 , GRCh37.p13 chr20: 50,093,862-50,099,452 NFATC2
    nsv5524287copy number variation1nstd206human GRCh38 chr20: 51,400,877-51,400,928 , GRCh37.p13 chr20: 50,017,414-50,017,465 NFATC2
    nsv5522505copy number variation1nstd206human GRCh38 chr20: 51,538,318-51,538,369 , GRCh37.p13 chr20: 50,154,857-50,154,908 NFATC2
    nsv5522449copy number variation1nstd206human GRCh38 chr20: 51,422,959-51,423,037 , GRCh37.p13 chr20: 50,039,496-50,039,574 NFATC2
    nsv5521048copy number variation1nstd206human GRCh38 chr20: 51,550,508-51,551,944 , GRCh37.p13 chr20: 50,167,047-50,168,483 NFATC2
    nsv5418418mobile element insertion1nstd206human GRCh38 chr20: 51,429,758-51,429,809 , GRCh37.p13 chr20: 50,046,295-50,046,346 NFATC2
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