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Items: 1 to 20 of 92

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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
    nsv5516992copy number variation1nstd206human GRCh38 chr19: 19,194,740-19,195,602 , GRCh37.p13 chr19: 19,305,549-19,306,411 RFXANK
    nsv5299782copy number variation1nstd204human GRCh38.p13 chr19: 18,706,301-19,688,800 , GRCh37.p13 chr19: 18,817,111-19,799,609 , HOMER3-AS1, 37 more genes
    nsv5290538copy number variation1nstd204human GRCh38.p13 chr19: 19,192,801-19,193,800 , GRCh37.p13 chr19: 19,303,610-19,304,609 RFXANK
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5019455copy number variation1nstd200human GRCh38 chr19: 19,194,509-19,195,962 , GRCh37.p13 chr19: 19,305,318-19,306,771 RFXANK
    nsv5014660copy number variation1nstd200human GRCh38 chr19: 19,105,820-19,389,022 , GRCh37.p13 chr19: 19,216,629-19,499,831 TMEM161A, HAPLN4, 12 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
    nsv4727917copy number variation1nstd197human GRCh38.p12 chr19: 19,199,155-19,201,719 , GRCh37 chr19: 19,309,964-19,312,528 RFXANK, NR2C2AP
    nsv4457454copy number variation1nstd102humanUncertain significance GRCh37 chr19: 19,230,490-19,440,304 , GRCh38.p12 chr19: 19,119,681-19,329,495 TM6SF2, NCAN, 10 more genes
    nsv4436023complex substitution1nstd102humanUncertain significance GRCh38.p12 chr19: 19,120,059-23,932,567 , GRCh37 chr19: 19,230,868-24,115,369 NCAN, BORCS8-MEF2B, 195 more genes
    nsv4268629copy number variation1nstd166human GRCh37.p13 chr19: 19,304,214-19,314,517 , GRCh38.p12 chr19: 19,193,405-19,203,708 RFXANK, NR2C2AP
    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
    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
    nsv3895942copy number variation1nstd102humanPathogenic GRCh37 chr19: 16,526,787-24,631,604 , GRCh38.p12 chr19: 16,415,976-24,448,802 BNIP3P37, ZNF675, 307 more genes
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