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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148135copy number variation1nstd102humanUncertain significance GRCh37 chr14: 57,675,327-59,806,898 , GRCh38.p12 chr14: 57,208,609-59,340,180 HMGB1P14, TOMM20L-DT, 36 more genes
    nsv7141593insertion1nstd232human GRCh37.p13 chr14: 58,875,888-58,875,888 , GRCh38.p12 chr14: 58,409,170-58,409,170 TIMM9, TOMM20L
    nsv7094499copy number variation1nstd102humanUncertain significance GRCh37 chr14: 58,894,347-58,899,195 , GRCh38.p12 chr14: 58,427,629-58,432,477 KIAA0586, TIMM9
    nsv7094435copy number variation1nstd102humanUncertain significance GRCh37 chr14: 58,894,347-59,014,694 , GRCh38.p12 chr14: 58,427,629-58,547,976 KIAA0586, HSBP1P1, 2 more genes
    nsv7069510inversion1nstd229human GRCh38 chr14: 57,948,807-58,720,869 , GRCh37.p13 chr14: 58,415,525-59,187,587 RN7SL598P, TRK-CTT1-1, 19 more genes
    nsv7060499inversion1nstd229human GRCh38 chr14: 57,927,850-58,665,319 , GRCh37.p13 chr14: 58,394,568-59,132,037 TOMM20L, KIAA0586, 19 more genes
    nsv7060471inversion1nstd229human GRCh38 chr14: 54,671,401-63,742,041 , GRCh37.p13 chr14: 55,138,119-64,208,759 KTN1, OTX2-AS1, 153 more genes
    nsv6957182copy number variation1nstd229human GRCh38 chr14: 58,399,240-58,408,526 , GRCh37.p13 chr14: 58,865,958-58,875,244 TOMM20L, TIMM9
    nsv6952443copy number variation1nstd229human GRCh38 chr14: 57,104,906-61,096,631 , GRCh37.p13 chr14: 57,571,624-61,563,349 LRRC9, RTN1, 71 more genes
    nsv6949011copy number variation1nstd229human GRCh38 chr14: 57,104,849-61,096,728 , GRCh37.p13 chr14: 57,571,567-61,563,446 MAD2L1P1, AP5M1, 71 more genes
    nsv6948339copy number variation1nstd229human GRCh38 chr14: 58,385,901-58,453,200 , GRCh37.p13 chr14: 58,852,619-58,919,918 TOMM20L, KIAA0586, 2 more genes
    nsv6947468copy number variation1nstd229human GRCh38 chr14: 58,392,263-58,406,829 , GRCh37.p13 chr14: 58,858,981-58,873,547 TIMM9, TOMM20L, 1 more genes
    nsv6938288copy number variation1nstd229human GRCh38 chr14: 58,424,517-58,456,632 , GRCh37.p13 chr14: 58,891,235-58,923,350 TIMM9, KIAA0586
    nsv6637688copy number variation1nstd102humanUncertain significance GRCh37 chr14: 58,833,909-59,109,480 , GRCh38.p12 chr14: 58,367,191-58,642,762 ARID4A, HNRNPCP1, 7 more genes
    nsv6637682copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 57,804,997-63,590,203 , GRCh38.p12 chr14: 57,338,279-63,123,485 PARP1P2, HIF1A, 91 more genes
    nsv6622788copy number variation1nstd224human GRCh37 chr14: 58,832,002-58,917,432 , GRCh38.p12 chr14: 58,365,284-58,450,714 KIAA0586, TOMM20L-DT, 3 more genes
    nsv6622787copy number variation1nstd224human GRCh37 chr14: 57,287,812-59,826,703 , GRCh38.p12 chr14: 56,821,094-59,359,985 KIAA0586, DAAM1, 41 more genes
    nsv6594267inversion1nstd223human GRCh38 chr14: 54,883,431-63,921,497 , GRCh37.p13 chr14: 55,350,149-64,388,215 RPL36AP1, GNRHR2P1, 152 more genes
    nsv6585900inversion1nstd223human GRCh38 chr14: 58,422,861-58,423,479 , GRCh37.p13 chr14: 58,889,579-58,890,197 TIMM9
    nsv6579120inversion1nstd223human GRCh38 chr14: 58,411,262-58,411,807 , GRCh37.p13 chr14: 58,877,980-58,878,525 TIMM9, TOMM20L
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