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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5284071copy number variation1nstd204human GRCh38.p13 chr19: 17,954,901-18,442,000 , GRCh37.p13 chr19: 18,065,710-18,552,810 ISYNA1, LOC105372300, 27 more genes
    nsv5282384copy number variation1nstd204human GRCh38.p13 chr19: 18,292,801-18,706,100 , GRCh37.p13 chr19: 18,403,611-18,816,910 ELL, FKBP8, 17 more genes
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 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
    nsv4673461copy number variation1nstd186human GRCh37 chr19: 18,539,501-18,549,500 , GRCh38.p12 chr19: 18,428,691-18,438,690 ISYNA1, SSBP4
    nsv4666362copy number variation1nstd186human GRCh37 chr19: 18,543,590-18,543,634 , GRCh38.p12 chr19: 18,432,780-18,432,824 ISYNA1, SSBP4
    nsv4634260copy number variation1nstd183human GRCh37 chr19: 18,544,591-18,545,153 , GRCh38.p12 chr19: 18,433,781-18,434,343 ISYNA1, SSBP4
    nsv4631357copy number variation1nstd183human GRCh37 chr19: 18,544,591-18,544,638 , GRCh38.p12 chr19: 18,433,781-18,433,828 ISYNA1, SSBP4
    nsv4623849copy number variation2nstd183human GRCh37 chr19: 18,543,590-18,543,634 , GRCh38.p12 chr19: 18,432,780-18,432,824 ISYNA1, SSBP4
    nsv4619579copy number variation1nstd183human GRCh37 chr19: 18,539,501-18,549,500 , GRCh38.p12 chr19: 18,428,691-18,438,690 ISYNA1, SSBP4
    nsv3959930insertion1nstd168human GRCh38 chr19: 18,421,206-18,466,056 , GRCh37.p13 chr19: 18,532,016-18,576,866 ELL, ISYNA1, 1 more genes
    nsv3922457copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,085,489-28,330,584 , GRCh38 chr19: 13,974,677-27,839,676 , NCBI36 chr19: 13,946,489-33,022,424 REX1BD, ZNF92P2, 416 more genes
    nsv3921076copy number variation1nstd102humanPathogenic GRCh38 chr19: 15,133,594-24,193,591 , GRCh37 chr19: 15,244,405-24,376,393 , NCBI36 chr19: 15,105,405-24,168,233 MRPL34, BNIP3P25, 358 more genes
    nsv3915387copy number variation1nstd102humanPathogenic GRCh37 chr19: 18,033,043-18,573,963 , NCBI36 chr19: 17,894,043-18,434,963 , GRCh38 chr19: 17,922,234-18,463,153 CSP3, LOC102725254, 28 more genes
    nsv3914228copy number variation1nstd102humanPathogenic NCBI36 chr19: 17,148,576-40,106,894 , GRCh38 chr19: 17,176,767-34,924,150 , GRCh37 chr19: 17,287,576-35,415,054 LOC105372355, SUGP2, 411 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 BCKDHA, ADGRE5, 1102 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
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