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Items: 1 to 20 of 176

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5530205copy number variation1nstd206human GRCh38 chr19: 33,813,278-33,813,335 , GRCh37.p13 chr19: 34,304,183-34,304,240 KCTD15
    nsv5525174copy number variation1nstd206human GRCh38 chr19: 33,425,684-34,028,349 , GRCh37.p13 chr19: 33,916,590-34,519,254 RPS4XP23, RN7SL150P, 8 more genes
    nsv5523202copy number variation1nstd206human GRCh38 chr19: 33,795,491-33,795,571 , GRCh37.p13 chr19: 34,286,396-34,286,476 KCTD15
    nsv5359734translocation1nstd200human GRCh38 chr19: 33,808,457-33,808,457 , GRCh38 chr19: 33,808,552-33,808,552 , GRCh37.p13 chr19: 34,299,457-34,299,457 , GRCh37.p13 chr19: 34,299,362-34,299,362 KCTD15
    nsv5359733translocation1nstd200human GRCh38 chr19: 33,795,571-33,795,571 , GRCh38 chr19: 33,795,491-33,795,491 , GRCh37.p13 chr19: 34,286,396-34,286,396 , GRCh37.p13 chr19: 34,286,476-34,286,476 KCTD15
    nsv5326384copy number variation1nstd204human GRCh38.p13 chr19: 33,795,488-33,795,573 , GRCh37.p13 chr19: 34,286,393-34,286,478 KCTD15
    nsv5020393copy number variation1nstd200human GRCh38 chr19: 33,804,958-33,805,239 , GRCh37.p13 chr19: 34,295,863-34,296,144 KCTD15
    nsv4631818copy number variation1nstd183human GRCh37 chr19: 34,291,467-34,291,623 , GRCh38.p12 chr19: 33,800,562-33,800,718 KCTD15
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4381295copy number variation1nstd173human GRCh37 chr19: 34,237,816-34,314,401 , GRCh38.p12 chr19: 33,746,911-33,823,496 CHST8, KCTD15
    nsv4261728copy number variation1nstd166human GRCh37.p13 chr19: 34,299,362-34,299,457 , GRCh38.p12 chr19: 33,808,457-33,808,552 KCTD15
    nsv4258785copy number variation1nstd166human GRCh37.p13 chr19: 34,295,350-34,295,415 , GRCh38.p12 chr19: 33,804,445-33,804,510 KCTD15
    nsv4254365copy number variation1nstd166human GRCh37.p13 chr19: 34,295,863-34,296,144 , GRCh38.p12 chr19: 33,804,958-33,805,239 KCTD15
    nsv3919618copy number variation1nstd102humanUncertain significance NCBI36 chr19: 32,962,986-39,966,686 , GRCh38 chr19: 27,780,238-34,783,942 , GRCh37 chr19: 28,271,146-35,274,846 LINC00906, TDRD12, 112 more genes
    nsv3919296copy number variation1nstd102humanPathogenic NCBI36 chr19: 34,844,605-43,297,203 , GRCh37 chr19: 30,152,765-38,605,363 , GRCh38 chr19: 29,661,858-38,114,723 UBA2, ZNF529, 241 more genes
    nsv3918197copy number variation1nstd102humanPathogenic GRCh38 chr19: 31,367,353-35,417,098 , NCBI36 chr19: 36,550,099-40,599,840 , GRCh37 chr19: 31,858,259-35,908,000 LINC01531, FXYD5, 110 more genes
    nsv3916007copy number variation1nstd102humanPathogenic GRCh37 chr19: 30,162,231-38,393,630 , NCBI36 chr19: 34,854,071-43,085,470 , GRCh38 chr19: 29,671,324-37,902,990 MAG, RNU6-967P, 238 more genes
    nsv3915971copy number variation1nstd102humanUncertain significance GRCh37 chr19: 34,229,318-34,488,947 , GRCh38 chr19: 33,738,413-33,998,042 , NCBI36 chr19: 38,921,158-39,180,787 RN7SL150P, CHST8, 1 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
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