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Items: 1 to 20 of 90

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095477copy number variation1nstd102humanUncertain significance GRCh37 chr19: 17,927,663-19,312,528 , GRCh38.p12 chr19: 17,816,854-19,201,719 BORCS8, ARMC6, 60 more genes
    nsv7076266inversion1nstd229human GRCh38 chr19: 19,130,894-20,543,167 , GRCh37.p13 chr19: 19,241,703-20,193,556 ZNF101, GATAD2A, 65 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
    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
    nsv7012541copy number variation1nstd229human GRCh38 chr19: 18,752,929-19,394,687 , GRCh37.p13 chr19: 18,863,739-19,505,496 SLC25A42, NCAN, 24 more genes
    nsv7010752copy number variation1nstd229human GRCh38 chr19: 19,105,820-19,389,022 , GRCh37.p13 chr19: 19,216,629-19,499,831 TMEM161A, HAPLN4, 12 more genes
    nsv6637313copy number variation1nstd102humanUncertain significance GRCh37 chr19: 19,218,464-19,494,045 , GRCh38.p12 chr19: 19,107,655-19,383,236 BORCS8-MEF2B, MAU2, 11 more genes
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6310474copy number variation1nstd102humanUncertain significance GRCh37 chr19: 18,893,725-19,312,528 , GRCh38.p12 chr19: 18,782,915-19,201,719 MEF2B, SLC25A42, 16 more genes
    nsv6310292copy number variation1nstd102humanUncertain significance GRCh37 chr19: 19,312,438-19,312,528 , GRCh38.p12 chr19: 19,201,629-19,201,719 RFXANK, NR2C2AP
    nsv6133402copy number variation1nstd213human GRCh37 chr19: 19,150,000-24,140,001 , GRCh38.p12 chr19: 19,039,191-23,957,199 , NCAN, 199 more genes
    nsv6133401copy number variation1nstd213human GRCh37 chr19: 19,110,000-24,140,001 , GRCh38.p12 chr19: 18,999,191-23,957,199 , NCAN, 200 more genes
    nsv6133400copy number variation1nstd213human GRCh37 chr19: 18,720,000-20,740,001 , GRCh38.p12 chr19: 18,609,190-20,557,195 COMP, NCAN, 81 more genes
    nsv6102553inversion1nstd212human GRCh38 chr19: 18,724,785-21,720,303 , GRCh37.p13 chr19: 18,835,595-21,903,105 , COMP, 127 more genes
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    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
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5014660copy number variation1nstd200human GRCh38 chr19: 19,105,820-19,389,022 , GRCh37.p13 chr19: 19,216,629-19,499,831 TMEM161A, HAPLN4, 12 more genes
    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
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