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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5927672copy number variation1nstd209human GRCh38 chr19: 18,886,091-18,886,257 , GRCh37.p13 chr19: 18,996,900-18,997,066 GDF1, CERS1
    nsv5585321copy number variation1nstd207human GRCh38 chr19: 18,886,091-18,886,255 , GRCh37.p13 chr19: 18,996,900-18,997,064 GDF1, CERS1
    nsv5521129copy number variation1nstd206human GRCh38 chr19: 18,886,091-18,886,266 , GRCh37.p13 chr19: 18,996,900-18,997,075 GDF1, CERS1
    nsv5516324copy number variation1nstd206human GRCh38 chr19: 18,889,852-18,889,910 , GRCh37.p13 chr19: 19,000,661-19,000,719 CERS1, GDF1
    nsv5381270copy number variation1nstd102humanUncertain significance GRCh37 chr19: 19,004,205-19,006,901 , GRCh38.p12 chr19: 18,893,396-18,896,092 GDF1, CERS1
    nsv5323434translocation1nstd204human GRCh37.p13 chr19: 18,981,771-18,981,771 , GRCh37.p13 chr19: 18,981,843-18,981,843 , GRCh38.p13 chr19: 18,870,962-18,870,962 , GRCh38.p13 chr19: 18,871,034-18,871,034 GDF1, CERS1
    nsv5322251copy number variation1nstd204human GRCh37.p13 chr19: 18,996,266-18,996,583 , GRCh38.p13 chr19: 18,885,457-18,885,774 CERS1, GDF1
    nsv5299782copy number variation1nstd204human GRCh38.p13 chr19: 18,706,301-19,688,800 , GRCh37.p13 chr19: 18,817,111-19,799,609 , HOMER3-AS1, 37 more genes
    nsv5171524mobile element insertion1nstd203human GRCh38 chr19: 18,885,699-18,885,743 , GRCh37.p13 chr19: 18,996,508-18,996,552 GDF1, CERS1
    nsv5161707mobile element insertion1nstd203human GRCh38 chr19: 18,885,440-18,885,467 , GRCh37.p13 chr19: 18,996,249-18,996,276 GDF1, CERS1
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5019440copy number variation1nstd200human GRCh38 chr19: 18,886,452-18,887,642 , GRCh37.p13 chr19: 18,997,261-18,998,451 GDF1, CERS1
    nsv4860648copy number variation1nstd200human GRCh37 chr19: 18,996,276-18,996,579 , GRCh38.p12 chr19: 18,885,467-18,885,770 CERS1, GDF1
    nsv4747868copy number variation1nstd199human GRCh37 chr19: 18,990,518-18,990,582 , GRCh38.p12 chr19: 18,879,709-18,879,773 GDF1, CERS1
    nsv4743589copy number variation1nstd199human GRCh37 chr19: 19,003,199-19,003,289 , GRCh38.p12 chr19: 18,892,390-18,892,480 CERS1, GDF1
    nsv4729750copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,286,624-20,956,753 , GRCh38.p12 chr19: 14,175,812-20,773,947 LOC105372309, RAB8A, 269 more genes
    nsv4667799copy number variation2nstd186human GRCh37 chr19: 18,992,932-18,993,171 , GRCh38.p12 chr19: 18,882,123-18,882,362 CERS1, GDF1
    nsv4643384copy number variation1nstd186human GRCh37 chr19: 18,996,900-18,997,075 , GRCh38.p12 chr19: 18,886,091-18,886,266 CERS1, GDF1
    nsv4633864copy number variation1nstd183human GRCh37 chr19: 18,993,112-18,993,266 , GRCh38.p12 chr19: 18,882,303-18,882,457 GDF1, CERS1
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