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Items: 1 to 20 of 98

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076302inversion1nstd229human GRCh38 chr14: 46,512,743-51,785,975 , GRCh37.p13 chr14: 46,981,946-52,252,693 LOC100420098, MAP4K5, 82 more genes
    nsv7070213inversion1nstd229human GRCh38 chr14: 49,862,783-49,875,348 , GRCh37.p13 chr14: 50,329,501-50,342,066 RN7SL2, LOC105378179
    nsv7063832inversion1nstd229human GRCh38 chr14: 49,825,608-49,875,466 , GRCh37.p13 chr14: 50,292,326-50,342,184 NEMF, RN7SL3, 3 more genes
    nsv7063700inversion1nstd229human GRCh38 chr14: 48,591,726-55,698,685 , GRCh37.p13 chr14: 49,060,929-56,165,403 ZFP64P1, LINC02331, 132 more genes
    nsv7059291inversion1nstd229human GRCh38 chr14: 49,838,942-56,572,993 , GRCh37.p13 chr14: 50,305,660-57,039,711 LOC105370500, LINC01599, 124 more genes
    nsv6956220copy number variation1nstd229human GRCh38 chr14: 49,783,631-49,862,929 , GRCh37.p13 chr14: 50,250,349-50,329,647 NEMF, RN7SL2, 4 more genes
    nsv6938412copy number variation1nstd229human GRCh38 chr14: 46,367,427-52,468,480 , GRCh37.p13 chr14: 46,836,630-52,935,198 RNU6-297P, RN7SL452P, 95 more genes
    nsv6578746inversion1nstd223human GRCh38 chr14: 49,838,941-56,572,992 , GRCh37.p13 chr14: 50,305,659-57,039,710 LOC100419913, TXNDC16, 124 more genes
    nsv6481699copy number variation1nstd223human GRCh38 chr14: 49,853,899-49,862,743 , GRCh37.p13 chr14: 50,320,617-50,329,461 RN7SL2, LOC105378179, 1 more genes
    nsv6480758copy number variation1nstd223human GRCh38 chr14: 49,853,709-49,862,689 , GRCh37.p13 chr14: 50,320,427-50,329,407 RN7SL2, LOC105378179, 1 more genes
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6314715copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884 HNRNPC, FOXG1, 616 more genes
    nsv6314025copy number variation1nstd102humanUncertain significance GRCh37 chr14: 45,827,312-50,529,931 , GRCh38.p12 chr14: 45,358,109-50,063,213 RPL18P1, RPL10L, 52 more genes
    nsv6133129copy number variation1nstd213human GRCh37 chr14: 50,170,000-50,350,001 , GRCh38.p12 chr14: 49,703,282-49,883,283 NEMF, KLHDC2, 5 more genes
    nsv5935089copy number variation1nstd209human GRCh38 chr14: 46,941,699-52,127,962 , GRCh37.p13 chr14: 47,410,902-52,594,680 , RNA5SP385, 92 more genes
    nsv5511932copy number variation1nstd206human GRCh38 chr14: 49,853,813-49,862,745 , GRCh37.p13 chr14: 50,320,531-50,329,463 RN7SL3, LOC105378179, 1 more genes
    nsv5305356copy number variation1nstd204human GRCh37.p13 chr14: 50,320,623-50,329,479 , GRCh38.p13 chr14: 49,853,905-49,862,761 RN7SL2, RN7SL3, 1 more genes
    nsv5279497copy number variation1nstd204human GRCh37.p13 chr14: 50,192,319-50,379,318 , GRCh38.p13 chr14: 49,725,601-49,912,600 ARF6, NEMF, 7 more genes
    nsv5269810copy number variation1nstd204human GRCh38.p13 chr14: 49,853,689-49,862,350 , GRCh37.p13 chr14: 50,320,407-50,329,068 RN7SL2, RN7SL3, 2 more genes
    nsv4840634copy number variation1nstd200human GRCh37 chr14: 50,320,403-50,329,442 , GRCh38.p12 chr14: 49,853,685-49,862,724 RN7SL2, LOC105378179, 2 more genes
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