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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5842618copy number variation1nstd209human GRCh38 chr5: 22,145,342-22,146,507 , GRCh37.p13 chr5: 22,145,451-22,146,616 PMCHL1, CDH12
    nsv5459844copy number variation1nstd206human GRCh38 chr5: 22,125,582-22,627,035 , GRCh37.p13 chr5: 22,125,691-22,627,144 PMCHL1, LOC105374681, 3 more genes
    nsv5459572copy number variation1nstd206human GRCh38 chr5: 22,152,402-22,161,678 , GRCh37.p13 chr5: 22,152,511-22,161,787 PMCHL1, CDH12
    nsv5381771copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716 OTULINL, AKTIPP2, 317 more genes
    nsv4793086copy number variation1nstd200human GRCh37 chr5: 22,142,750-22,142,987 , GRCh38.p12 chr5: 22,142,641-22,142,878 PMCHL1, CDH12
    nsv4762598inversion1nstd199human GRCh37 chr5: 20,832,595-34,371,602 , GRCh38.p12 chr5: 20,832,486-34,371,497 , CDH6, 117 more genes
    nsv4752323inversion1nstd199human GRCh37 chr5: 21,523,122-29,424,248 , GRCh38.p12 chr5: 21,523,013-29,424,141 , CDH9, 49 more genes
    nsv4751404inversion1nstd199human GRCh37 chr5: 20,834,824-34,371,606 , GRCh38.p12 chr5: 20,834,715-34,371,501 , CDH6, 117 more genes
    nsv4729109copy number variation1nstd102humanUncertain significance GRCh37 chr5: 16,741,484-23,963,898 , GRCh38.p12 chr5: 16,741,375-23,963,789 LOC105374672, LOC105374669, 70 more genes
    nsv4728817copy number variation1nstd102humanUncertain significance GRCh37 chr5: 19,324,003-30,115,028 , GRCh38.p12 chr5: 19,323,894-30,114,921 LOC100533667, LOC105374672, 70 more genes
    nsv4674495copy number variation1nstd102humanUncertain significance GRCh37 chr5: 20,002,584-22,393,176 , GRCh38.p12 chr5: 20,002,475-22,393,067 LOC100419319, LOC105374685, 17 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
    nsv4590895copy number variation1nstd183human GRCh37 chr5: 22,089,307-22,152,534 , GRCh38.p12 chr5: 22,089,198-22,152,425 CDH12, PMCHL1
    nsv4590894copy number variation1nstd183human GRCh37 chr5: 21,989,556-23,446,583 , GRCh38.p12 chr5: 21,989,447-23,446,474 LOC105374682, GCNT1P2, 9 more genes
    nsv4590872copy number variation1nstd183human GRCh37 chr5: 21,986,878-23,447,978 , GRCh38.p12 chr5: 21,986,769-23,447,869 LOC100420804, LOC105374687, 9 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
    nsv4404644copy number variation1nstd174human GRCh37 chr5: 21,989,556-24,131,279 , GRCh38.p12 chr5: 21,989,447-24,131,170 GCNT1P2, LOC105374688, 12 more genes
    nsv4395643copy number variation1nstd174human GRCh37 chr5: 22,127,047-22,247,299 , GRCh38.p12 chr5: 22,126,938-22,247,190 CDH12, PMCHL1, 1 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
    nsv4131487copy number variation1nstd166human GRCh37.p13 chr5: 22,143,658-22,148,927 , GRCh38.p12 chr5: 22,143,549-22,148,818 CDH12, PMCHL1
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