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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112768copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,984,696-46,405,042 , GRCh38.p12 chr5: 34,984,591-46,404,940 LIFR-AS1, FGF10-AS1, 137 more genes
    nsv5906638copy number variation1nstd209human GRCh38 chr5: 36,104,957-36,105,027 , GRCh37.p13 chr5: 36,105,059-36,105,129 LMBRD2
    nsv5896622copy number variation1nstd209human GRCh38 chr5: 36,120,103-36,121,021 , GRCh37.p13 chr5: 36,120,205-36,121,123 LMBRD2
    nsv5681940mobile element insertion1nstd211human GRCh38 chr5: 36,105,849-36,105,849 , GRCh37.p13 chr5: 36,105,951-36,105,951 LMBRD2
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5469415copy number variation1nstd206human GRCh38 chr5: 36,104,957-36,105,028 , GRCh37.p13 chr5: 36,105,059-36,105,130 LMBRD2
    nsv5407358mobile element insertion1nstd206human GRCh38 chr5: 36,105,849-36,105,900 , GRCh37.p13 chr5: 36,105,951-36,106,002 LMBRD2
    nsv5381781copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,081,195-45,294,031 , GRCh38.p12 chr5: 29,081,088-45,293,929 ST3GAL5P1, LOC105374711, 213 more genes
    nsv5093017mobile element insertion1nstd203human GRCh38 chr5: 36,137,979-36,137,995 , GRCh37.p13 chr5: 36,138,081-36,138,097 LMBRD2
    nsv4674057copy number variation1nstd102humanUncertain significance GRCh37 chr5: 35,382,352-36,123,330 , GRCh38.p12 chr5: 35,382,250-36,123,228 CAPSL, CAPSL-DT, 7 more genes
    nsv4569390sequence alteration1nstd166human GRCh37.p13 chr5: 36,152,256-36,160,529 , GRCh38.p12 chr5: 36,152,154-36,160,427 SKP2, LMBRD2, 1 more genes
    nsv4521992copy number variation1nstd166human GRCh37.p13 chr5: 36,120,205-36,121,127 , GRCh38.p12 chr5: 36,120,103-36,121,025 LMBRD2
    nsv4477815mobile element insertion1nstd166human GRCh37.p13 chr5: 36,138,081-36,138,081 , GRCh38.p12 chr5: 36,137,979-36,137,979 LMBRD2
    nsv4456866copy number variation1nstd102humanPathogenic GRCh37 chr5: 34,453,883-46,389,339 , GRCh38.p12 chr5: 34,453,778-46,389,237 LOC100506639, EEF1A1P19, 146 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4130779copy number variation1nstd166human GRCh37.p13 chr5: 36,105,059-36,105,130 , GRCh38.p12 chr5: 36,104,957-36,105,028 LMBRD2
    nsv4127209copy number variation1nstd166human GRCh37.p13 chr5: 36,103,444-36,103,563 , GRCh38.p12 chr5: 36,103,342-36,103,461 LMBRD2
    nsv3923992copy number variation1nstd102humanPathogenic GRCh37 chr5: 50,093-46,115,086 , NCBI36 chr5: 103,093-46,150,843 , GRCh38 chr5: 49,978-46,114,984 LOC100130748, CDH10, 533 more genes
    nsv3920391copy number variation1nstd102humanPathogenic GRCh38 chr5: 35,201,559-61,903,141 , GRCh37 chr5: 35,201,661-61,198,968 , NCBI36 chr5: 35,237,418-61,234,725 KRT18P56, LINC01265, 290 more genes
    nsv3918728copy number variation1nstd102humanPathogenic GRCh38 chr5: 4,849,498-36,818,719 , NCBI36 chr5: 4,902,611-36,854,578 , GRCh37 chr5: 4,849,611-36,818,821 LINC02100, FTH1P10, 334 more genes
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