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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142416copy number variation1nstd232human GRCh37.p13 chr19: 3,455,523-3,455,601 , GRCh38.p12 chr19: 3,455,525-3,455,603 NFIC
    nsv7098718copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,206,913-3,771,740 , GRCh38.p12 chr19: 1,206,914-3,771,742 GIPC3, GNG7, 117 more genes
    nsv7095297copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777 NCLN, RN7SL202P, 223 more genes
    nsv7095226copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-4,818,389 , GRCh38.p12 chr19: 589,946-4,818,377 ATP5F1D, LOC102723798, 204 more genes
    nsv7076900inversion1nstd229human GRCh38 chr19: 3,358,040-3,358,177 , GRCh37.p13 chr19: 3,358,038-3,358,175 NFIC
    nsv7070316inversion1nstd229human GRCh38 chr19: 3,349,620-3,668,217 , GRCh37.p13 chr19: 3,349,618-3,668,215 PIP5K1C, LOC105372245, 12 more genes
    nsv7070232inversion1nstd229human GRCh38 chr19: 3,392,155-3,396,027 , GRCh37.p13 chr19: 3,392,153-3,396,025 NFIC
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 more genes
    nsv7065682inversion1nstd229human GRCh38 chr19: 3,282,406-3,593,791 , GRCh37.p13 chr19: 3,282,404-3,593,789 CELF5, NFIC, 11 more genes
    nsv7061236inversion1nstd229human GRCh38 chr19: 3,356,784-3,358,172 , GRCh37.p13 chr19: 3,356,782-3,358,170 NFIC
    nsv7012970copy number variation1nstd229human GRCh38 chr19: 3,370,556-3,371,999 , GRCh37.p13 chr19: 3,370,554-3,371,997 NFIC
    nsv7010524copy number variation1nstd229human GRCh38 chr19: 3,449,728-3,548,918 , GRCh37.p13 chr19: 3,449,726-3,548,916 FZR1, MFSD12, 6 more genes
    nsv7010387copy number variation1nstd229human GRCh38 chr19: 3,391,060-3,396,767 , GRCh37.p13 chr19: 3,391,058-3,396,765 NFIC
    nsv7009125copy number variation1nstd229human GRCh38 chr19: 3,467,726-3,474,695 , GRCh37.p13 chr19: 3,467,724-3,474,693 SMIM24, NFIC
    nsv7008578copy number variation1nstd229human GRCh38 chr19: 3,376,831-3,379,535 , GRCh37.p13 chr19: 3,376,829-3,379,533 NFIC
    nsv7007860copy number variation1nstd229human GRCh38 chr19: 3,417,995-3,423,167 , GRCh37.p13 chr19: 3,417,993-3,423,165 NFIC
    nsv7005708copy number variation1nstd229human GRCh38 chr19: 3,370,666-3,370,723 , GRCh37.p13 chr19: 3,370,664-3,370,721 NFIC
    nsv7003616copy number variation1nstd229human GRCh38 chr19: 3,393,576-3,395,076 , GRCh37.p13 chr19: 3,393,574-3,395,074 NFIC
    nsv7003129copy number variation1nstd229human GRCh38 chr19: 3,417,247-3,420,993 , GRCh37.p13 chr19: 3,417,245-3,420,991 NFIC
    nsv7000677copy number variation1nstd229human GRCh38 chr19: 3,419,701-3,424,000 , GRCh37.p13 chr19: 3,419,699-3,423,998 NFIC
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