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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095645copy number variation1nstd102humanUncertain significance GRCh37 chr19: 14,847,048-17,394,124 , GRCh38.p12 chr19: 14,736,236-17,283,315 HAUS8, MIR1470, 95 more genes
    nsv7075473inversion1nstd229human GRCh38 chr19: 12,694,752-17,614,167 , GRCh37.p13 chr19: 12,805,566-17,724,976 SYDE1, LOC107985287, 207 more genes
    nsv7065580inversion1nstd229human GRCh38 chr19: 11,963,576-20,150,892 , GRCh37.p13 chr19: 12,074,391-20,193,556 CYP4F24P, CYP4F2, 359 more genes
    nsv7063135inversion1nstd229human GRCh38 chr19: 12,625,698-17,530,884 , GRCh37.p13 chr19: 12,736,512-17,641,693 SYCE2, OR1AB1P, 212 more genes
    nsv7060542inversion1nstd229human GRCh38 chr19: 12,342,956-19,691,233 , GRCh37.p13 chr19: 12,453,770-19,802,042 DDX39A, KCNN1, 314 more genes
    nsv7059139inversion1nstd229human GRCh38 chr19: 12,641,624-19,910,103 , GRCh37.p13 chr19: 12,752,438-20,020,912 NR2F6, ISCA1P5, 307 more genes
    nsv7009063copy number variation1nstd229human GRCh38 chr19: 17,207,614-17,239,395 , GRCh37.p13 chr19: 17,318,423-17,350,204 USE1, MYO9B, 2 more genes
    nsv7005523copy number variation1nstd229human GRCh38 chr19: 17,218,305-17,232,786 , GRCh37.p13 chr19: 17,329,114-17,343,595 USE1, OCEL1, 1 more genes
    nsv7004911copy number variation1nstd229human GRCh38 chr19: 16,817,573-17,564,195 , GRCh37.p13 chr19: 16,928,384-17,675,004 BISPR, NWD1, 32 more genes
    nsv7000416copy number variation1nstd229human GRCh38 chr19: 17,240,841-17,259,269 , GRCh37.p13 chr19: 17,351,650-17,370,078 USHBP1, NR2F6
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6531234copy number variation1nstd223human GRCh38 chr19: 17,229,406-17,233,620 , GRCh37.p13 chr19: 17,340,215-17,344,429 OCEL1, NR2F6
    nsv6520443copy number variation1nstd223human GRCh38 chr19: 17,223,966-17,263,133 , GRCh37.p13 chr19: 17,334,775-17,373,942 NR2F6, OCEL1, 1 more genes
    nsv6133691copy number variation1nstd213human GRCh37 chr19: 15,360,000-18,450,001 , GRCh38.p12 chr19: 15,249,189-18,339,191 BST2, NR2F6, 123 more genes
    nsv6133521copy number variation1nstd213human GRCh37 chr19: 17,200,000-17,780,001 , GRCh38.p12 chr19: 17,089,190-17,669,192 ANO8, OCEL1, 27 more genes
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5699686mobile element insertion2nstd211human GRCh38 chr19: 17,233,349-17,233,349 , GRCh37.p13 chr19: 17,344,158-17,344,158 NR2F6
    nsv5299651copy number variation1nstd204human GRCh38.p13 chr19: 16,996,101-18,292,600 , GRCh37.p13 chr19: 17,106,911-18,403,410 ANO8, MPV17L2, 57 more genes
    nsv5293042copy number variation1nstd204human GRCh38.p13 chr19: 17,178,501-17,350,400 , GRCh37.p13 chr19: 17,289,310-17,461,209 NR2F6, ABHD8, 11 more genes
    nsv5287174copy number variation1nstd204human GRCh38.p13 chr19: 17,237,488-17,238,504 , GRCh37.p13 chr19: 17,348,297-17,349,313 NR2F6
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