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Items: 1 to 20 of 187

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 more genes
    nsv7060352inversion1nstd229human GRCh38 chr19: 3,851,263-4,364,229 , GRCh37.p13 chr19: 3,851,261-4,364,226 DAPK3, YJU2, 22 more genes
    nsv7015810copy number variation1nstd229human GRCh38 chr19: 4,231,601-4,238,100 , GRCh37.p13 chr19: 4,231,598-4,238,097 EBI3
    nsv6624973copy number variation1nstd224human GRCh37 chr19: 4,180,801-4,288,333 , GRCh38.p12 chr19: 4,180,804-4,288,336 EBI3, SIRT6, 3 more genes
    nsv6597296inversion1nstd223human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , ALKBH7, 192 more genes
    nsv6525236copy number variation1nstd223human GRCh38 chr19: 4,230,264-4,269,121 , GRCh37.p13 chr19: 4,230,261-4,269,118 EBI3, YJU2
    nsv6525134copy number variation1nstd223human GRCh38 chr19: 4,230,611-4,240,366 , GRCh37.p13 chr19: 4,230,608-4,240,363 EBI3
    nsv6523984copy number variation1nstd223human GRCh38 chr19: 4,230,455-4,231,273 , GRCh37.p13 chr19: 4,230,452-4,231,270 EBI3
    nsv6522042copy number variation1nstd223human GRCh38 chr19: 4,228,136-4,228,969 , GRCh37.p13 chr19: 4,228,133-4,228,966 EBI3
    nsv6291587copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,501,624-5,357,124 , GRCh38.p12 chr19: 3,501,626-5,357,113 RN7SL202P, EIF1P6, 67 more genes
    nsv6291557copy number variation1nstd102humanUncertain significance GRCh37 chr19: 4,182,912-4,633,772 , GRCh38.p12 chr19: 4,182,915-4,633,760 STAP2, MIR4746, 19 more genes
    nsv6282266copy number variation1nstd214human GRCh38 chr19: 4,228,433-4,228,507 , GRCh37.p13 chr19: 4,228,430-4,228,504 EBI3
    nsv6207445copy number variation1nstd214human GRCh38 chr19: 4,228,337-4,228,425 , GRCh37.p13 chr19: 4,228,334-4,228,422 EBI3
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133468copy number variation1nstd213human GRCh37 chr19: 2,040,000-7,300,001 , GRCh38.p12 chr19: 2,040,001-7,299,990 TLE5, AMH, 192 more genes
    nsv6112338insertion1nstd212human GRCh38 chr19: 4,234,205-4,234,205 , GRCh37.p13 chr19: 4,234,202-4,234,202 EBI3
    nsv6108220insertion1nstd212human GRCh38 chr19: 4,228,367-4,228,367 , GRCh37.p13 chr19: 4,228,364-4,228,364 EBI3
    nsv6107625insertion1nstd212human GRCh38 chr19: 4,228,968-4,228,968 , GRCh37.p13 chr19: 4,228,965-4,228,965 EBI3
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