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Items: 1 to 20 of 209

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5473082copy number variation1nstd206human GRCh38 chr5: 7,798,999-8,835,000 , GRCh37.p13 chr5: 7,799,112-8,835,112 ADCY2, LOC102723339, 13 more genes
    nsv5469428copy number variation1nstd206human GRCh38 chr5: 8,460,278-8,460,333 , GRCh37.p13 chr5: 8,460,391-8,460,446 MIR4458, MIR4458HG
    nsv5381771copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716 OTULINL, AKTIPP2, 317 more genes
    nsv5377870translocation1nstd200human GRCh38 chr5: 8,463,766-8,463,766 , GRCh38 chr5: 8,457,449-8,457,449 , GRCh37.p13 chr5: 8,457,562-8,457,562 , GRCh37.p13 chr5: 8,463,879-8,463,879 LINC02226, MIR4458HG
    nsv5340414translocation1nstd200human GRCh37 chr5: 8,457,562-8,457,562 , GRCh37 chr5: 8,463,879-8,463,879 , GRCh38.p12 chr5: 8,463,766-8,463,766 , GRCh38.p12 chr5: 8,457,449-8,457,449 LINC02226, MIR4458HG
    nsv5041416inversion1nstd200human GRCh38 chr5: 6,583,518-8,812,732 , GRCh37.p13 chr5: 6,583,631-8,812,844 RNA5SP176, MTND6P2, 36 more genes
    nsv4685752copy number variation1nstd102humanPathogenic GRCh37 chr5: 71,904-22,078,969 , GRCh38.p12 chr5: 71,789-22,078,860 LINC01377, LOC100421308, 277 more genes
    nsv4674497copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-14,738,180 , GRCh38.p12 chr5: 113,461-14,738,071 LOC101929003, MTCYBP37, 192 more genes
    nsv4674478copy number variation1nstd102humanUncertain significance GRCh37 chr5: 7,952,706-9,108,420 , GRCh38.p12 chr5: 7,952,593-9,108,308 LINC02199, RNU1-76P, 11 more genes
    nsv4674444copy number variation1nstd102humanPathogenic GRCh37 chr5: 1,322,680-10,762,544 , GRCh38.p12 chr5: 1,322,565-10,762,432 LOC100132773, LINC01019, 125 more genes
    nsv4674169copy number variation1nstd102humanUncertain significance GRCh37 chr5: 7,882,916-9,827,532 , GRCh38.p12 chr5: 7,882,803-9,827,420 LOC101929359, MTND6P2, 21 more genes
    nsv4674161copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-23,364,376 , GRCh38.p12 chr5: 113,461-23,364,267 LOC102723561, LOC107986397, 287 more genes
    nsv4674130copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-11,767,720 , GRCh38.p12 chr5: 113,461-11,767,608 SLC9A3-AS1, LINC02114, 169 more genes
    nsv4591746copy number variation1nstd183human GRCh37 chr5: 8,454,699-8,469,309 , GRCh38.p12 chr5: 8,454,586-8,469,196 MIR4458, LOC100419318, 2 more genes
    nsv4523697copy number variation1nstd166human GRCh37.p13 chr5: 8,259,999-8,737,000 , GRCh38.p12 chr5: 8,259,886-8,736,888 LINC02226, LOC100419318, 5 more genes
    nsv4477799mobile element insertion1nstd166human GRCh37.p13 chr5: 8,460,904-8,460,904 , GRCh38.p12 chr5: 8,460,791-8,460,791 MIR4458, MIR4458HG
    nsv4456720copy number variation1nstd102humanUncertain significance GRCh37 chr5: 7,607,935-9,584,194 , GRCh38.p12 chr5: 7,607,822-9,584,082 MIR4458, SNORD123, 19 more genes
    nsv4369315copy number variation1nstd173human GRCh37 chr5: 113,577-10,304,966 , GRCh38.p12 chr5: 113,462-10,304,854 , LOC105374625, 158 more genes
    nsv4365160copy number variation1nstd173human GRCh37 chr5: 8,073,855-9,010,370 , GRCh38.p12 chr5: 8,073,742-9,010,258 LOC102723339, LOC101929307, 8 more genes
    nsv4349271copy number variation1nstd102humanPathogenic GRCh37 chr5: 140,474-26,906,925 , GRCh38.p12 chr5: 140,359-26,906,816 MIR4636, LRRC14B, 304 more genes
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