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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142495copy number variation1nstd232human GRCh37.p13 chr19: 1,011,990-1,012,062 , GRCh38.p12 chr19: 1,011,991-1,012,063 TMEM259
    nsv7138924copy number variation1nstd232human GRCh37.p13 chr19: 1,011,497-1,011,576 , GRCh38.p12 chr19: 1,011,498-1,011,577 TMEM259
    nsv7095297copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777 NCLN, RN7SL202P, 223 more genes
    nsv7095296copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-2,151,333 , GRCh38.p12 chr19: 589,946-2,151,334 ADAMTSL5, GPX4, 90 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
    nsv7075040inversion1nstd229human GRCh38 chr19: 1,008,243-1,021,190 , GRCh37.p13 chr19: 1,008,242-1,021,189 LOC105372235, RNU6-2, 2 more genes
    nsv7073568inversion1nstd229human GRCh38 chr19: 996,281-1,021,192 , GRCh37.p13 chr19: 996,280-1,021,191 GRIN3B, LOC105372235, 2 more genes
    nsv7073159inversion1nstd229human GRCh38 chr19: 249,047-1,189,238 , GRCh37.p13 chr19: 249,047-1,189,237 MADCAM1-AS1, ARID3A, 53 more genes
    nsv7064913inversion1nstd229human GRCh38 chr19: 558,352-1,188,612 , GRCh37.p13 chr19: 558,352-1,188,611 MIR4745, R3HDM4, 40 more genes
    nsv7017136copy number variation1nstd229human GRCh38 chr19: 976,018-1,035,211 , GRCh37.p13 chr19: 976,018-1,035,210 TMEM259, CNN2, 5 more genes
    nsv7016558copy number variation1nstd229human GRCh38 chr19: 957,195-1,039,723 , GRCh37.p13 chr19: 957,195-1,039,722 CNN2, WDR18, 6 more genes
    nsv7015593copy number variation1nstd229human GRCh38 chr19: 996,301-1,008,300 , GRCh37.p13 chr19: 996,300-1,008,299 TMEM259, GRIN3B, 1 more genes
    nsv7010900copy number variation1nstd229human GRCh38 chr19: 1,015,397-1,037,860 , GRCh37.p13 chr19: 1,015,396-1,037,859 CNN2, RNU6-2, 1 more genes
    nsv7009328copy number variation1nstd229human GRCh38 chr19: 1,008,301-1,010,600 , GRCh37.p13 chr19: 1,008,300-1,010,599 LOC105372235, GRIN3B, 1 more genes
    nsv7008367copy number variation1nstd229human GRCh38 chr19: 1,015,733-1,015,998 , GRCh37.p13 chr19: 1,015,732-1,015,997 TMEM259
    nsv7007571copy number variation1nstd229human GRCh38 chr19: 1,017,064-1,023,837 , GRCh37.p13 chr19: 1,017,063-1,023,836 RNU6-2, TMEM259
    nsv7001912copy number variation1nstd229human GRCh38 chr19: 1,013,071-1,018,187 , GRCh37.p13 chr19: 1,013,070-1,018,186 TMEM259
    nsv7000995copy number variation1nstd229human GRCh38 chr19: 1,001,307-1,019,726 , GRCh37.p13 chr19: 1,001,306-1,019,725 RNU6-2, LOC105372235, 2 more genes
    nsv6624425copy number variation1nstd224human GRCh37 chr19: 1,013,021-1,049,396 , GRCh38.p12 chr19: 1,013,022-1,049,397 CNN2, RNU6-2, 2 more genes
    nsv6597832inversion1nstd223human GRCh38 chr19: 558,351-1,188,654 , GRCh37.p13 chr19: 558,351-1,188,653 HCN2, TMEM259, 40 more genes
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