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Items: 12

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    Number of Variants: 12

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3905649copy number variation1nstd102humanUncertain significance GRCh37 chr19: 44,624,036-44,713,584 , GRCh38.p12 chr19: 44,119,883-44,209,431 ZNF234, ZNF227, 2 more genes
    nsv3891669copy number variation1nstd102humanPathogenic GRCh37 chr19: 43,013,365-47,241,534 , GRCh38.p12 chr19: 42,509,213-46,738,277 ZNF234, MIR320E, 189 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF234, ZNF321P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 ZNF234, BABAM1, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 ZNF234, LENG8, 2408 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 ZNF234, BCKDHA, 1102 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF234, ZNF461, 735 more genes
    nsv3880735copy number variation1nstd102humanLikely pathogenic GRCh38 chr19: 41,608,672-44,315,856 , GRCh37.p13 chr19: 42,514,712-44,820,009 ZNF234, ATP1A3, 114 more genes
    nsv3890841copy number variation1nstd102humanUncertain significance GRCh37 chr19: 44,300,416-45,639,540 , GRCh38.p12 chr19: 43,796,264-45,136,282 ZNF234, ZNF225, 57 more genes
    nsv1398140copy number variation1nstd102humanUncertain significance GRCh37 chr19: 44,466,919-45,029,206 , GRCh38.p12 chr19: 43,962,767-44,525,173 ZNF234, CEACAM20, 23 more genes
    nsv7095657copy number variation1nstd102humanUncertain significance GRCh37 chr19: 44,011,002-45,213,778 , GRCh38.p12 chr19: 43,506,850-44,710,506 ZNF234, RN7SL368P, 52 more genes
    nsv4436634complex substitution1nstd102humanUncertain significance GRCh38.p12 chr19: 43,997,366-44,819,487 , GRCh37 chr19: 44,501,518-45,322,744 ZNF234, BCL3, 34 more genes
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