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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5725917mobile element insertion1nstd211human GRCh38 chr19: 29,817,101-29,817,101 , GRCh37.p13 chr19: 30,308,008-30,308,008 CCNE1
    nsv5024519copy number variation1nstd200human GRCh38 chr19: 28,925,173-32,768,971 , GRCh37.p13 chr19: 29,416,080-33,259,877 , LOC105372355, 53 more genes
    nsv4729940copy number variation1nstd102humanUncertain significance GRCh37 chr19: 29,739,728-31,053,524 , GRCh38.p12 chr19: 29,248,821-30,562,617 PLEKHF1, RPL9P32, 12 more genes
    nsv4705277copy number variation1nstd195human GRCh37 chr19: 30,210,851-30,388,801 , GRCh38.p12 chr19: 29,719,944-29,897,894 CCNE1, LOC107985345
    nsv4630420copy number variation1nstd183human GRCh37 chr19: 27,749,407-30,499,419 , GRCh38.p12 chr19: 27,258,499-30,008,512 , C19orf12, 32 more genes
    nsv4629987copy number variation2nstd183human GRCh37 chr19: 30,302,842-30,303,497 , GRCh38.p12 chr19: 29,811,935-29,812,590 CCNE1
    nsv4622031copy number variation1nstd183human GRCh37 chr19: 30,302,842-30,302,897 , GRCh38.p12 chr19: 29,811,935-29,811,990 CCNE1
    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
    nsv4376090copy number variation1nstd173human GRCh37 chr19: 30,279,968-30,624,835 , GRCh38.p12 chr19: 29,789,061-30,133,928 URI1, CCNE1, 4 more genes
    nsv4368202copy number variation1nstd173human GRCh37 chr19: 30,283,529-30,624,835 , GRCh38.p12 chr19: 29,792,622-30,133,928 URI1, TAF9P3, 4 more genes
    nsv4268071copy number variation1nstd166human GRCh37.p13 chr19: 30,306,083-30,306,306 , GRCh38.p12 chr19: 29,815,176-29,815,399 CCNE1
    nsv3920776copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 34,234,635-37,150,342 , GRCh37 chr19: 29,542,795-32,458,502 , GRCh38 chr19: 29,051,888-31,967,596 CCNE1, UQCRFS1, 30 more genes
    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
    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
    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
    nsv3908619copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 28,271,107-31,110,233 , GRCh38.p12 chr19: 27,780,199-30,619,326 CCNE1, UQCRFS1, 31 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
    nsv3903946copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 30,112,378-31,939,682 , GRCh38.p12 chr19: 29,621,471-31,448,776 CCNE1, URI1, 17 more genes
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