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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094244copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,915,399-22,005,055 , GRCh38.p12 chr14: 20,447,240-21,536,921 ARHGEF40, LOC105370398, 78 more genes
    nsv7072621inversion1nstd229human GRCh38 chr14: 20,991,576-21,885,954 , GRCh37.p13 chr14: 21,459,735-22,354,136 LINC00641, TRAV13-1, 61 more genes
    nsv7058177inversion1nstd229human GRCh38 chr14: 21,098,135-21,342,114 , GRCh37.p13 chr14: 21,566,294-21,810,273 RNU6-252P, ZNF219, 11 more genes
    nsv6950901copy number variation1nstd229human GRCh38 chr14: 21,099,459-21,186,340 , GRCh37.p13 chr14: 21,567,618-21,654,499 RNU6-252P, ZNF219, 7 more genes
    nsv6941683copy number variation1nstd229human GRCh38 chr14: 21,103,650-21,107,015 , GRCh37.p13 chr14: 21,571,809-21,575,174 TMEM253, ZNF219
    nsv6637860copy number variation1nstd102humanUncertain significance GRCh37 chr14: 21,496,133-21,962,265 , GRCh38.p12 chr14: 21,027,974-21,494,106 ARHGEF40, RN7SL650P, 28 more genes
    nsv6637326copy number variation1nstd102humanUncertain significance GRCh37 chr14: 21,349,608-21,618,292 , GRCh38.p12 chr14: 20,881,449-21,150,133 RNASE13, ARHGEF40, 21 more genes
    nsv6637318copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,690,196-23,114,522 , GRCh38.p12 chr14: 20,222,037-22,645,313 TRAJ21, TRAJ44, 239 more genes
    nsv6478520copy number variation1nstd223human GRCh38 chr14: 21,018,228-21,399,161 , GRCh37.p13 chr14: 21,486,387-21,867,320 SUPT16H, LOC105370398, 25 more genes
    nsv6315513copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-47,481,203 , GRCh38.p12 chr14: 20,043,513-47,012,000 CDH24, KLHL33, 623 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
    nsv6314121copy number variation1nstd102humanUncertain significance GRCh37 chr14: 21,451,544-21,962,317 , GRCh38.p12 chr14: 20,983,385-21,494,158 ZNF219, EIF4EBP1P1, 33 more genes
    nsv6290276copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 20,925,965-23,649,548 , GRCh38.p12 chr14: 20,457,806-23,180,339 ANG, APEX1, 255 more genes
    nsv6132583copy number variation1nstd213human GRCh37 chr14: 20,420,000-22,590,001 , GRCh38.p12 chr14: 19,951,841-22,122,043 HNRNPC, PNP, 157 more genes
    nsv5709036mobile element insertion2nstd211human GRCh38 chr14: 21,099,011-21,099,011 , GRCh37.p13 chr14: 21,567,170-21,567,170 ZNF219, TMEM253
    nsv5428986mobile element insertion1nstd206human GRCh38 chr14: 21,099,011-21,099,062 , GRCh37.p13 chr14: 21,567,170-21,567,221 ZNF219, TMEM253
    nsv4729394copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-21,915,516 , GRCh38.p12 chr14: 20,043,513-21,447,357 SETP1, OR11H5P, 99 more genes
    nsv4685750copy number variation1nstd102humannot provided GRCh37 chr14: 20,511,672-42,881,888 , GRCh38.p12 chr14: 20,043,513-42,412,685 IGBP1P1, RAB2B, 579 more genes
    nsv4676085copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,143,933-23,297,667 , GRCh38.p12 chr14: 20,675,774-22,828,458 ANG, SNORD8, 209 more genes
    nsv4675977copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 21,159,605-22,252,320 , GRCh38.p12 chr14: 20,691,446-21,784,103 ANG, HNRNPC, 69 more genes
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