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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7040713inversion1nstd229human GRCh38 chr5: 44,325,839-45,047,347 , GRCh37.p13 chr5: 44,325,941-45,047,449 MRPS30, FGF10, 4 more genes
    nsv6763902copy number variation1nstd229human GRCh38 chr5: 44,407,953-44,408,260 , GRCh37.p13 chr5: 44,408,055-44,408,362 FGF10-AS1
    nsv6636973copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,348,753-46,389,339 , GRCh38.p12 chr5: 29,348,646-46,389,237 SUB1, LOC105374740, 210 more genes
    nsv6395196copy number variation1nstd223human GRCh38 chr5: 44,400,201-44,401,400 , GRCh37.p13 chr5: 44,400,303-44,401,502 FGF10-AS1
    nsv6315368copy number variation1nstd102humanPathogenic GRCh37 chr5: 36,053,583-46,389,339 , GRCh38.p12 chr5: 36,053,481-46,389,237 C7, RIMOC1, 128 more genes
    nsv6315286copy number variation1nstd102humanUncertain significance GRCh38 chr5: 44,375,961-44,815,730 , GRCh37.p13 chr5: 44,376,063-44,815,832 FGF10-AS1, LINC02224, 4 more genes
    nsv6313864copy number variation1nstd102humanPathogenic GRCh37 chr5: 26,382,110-46,389,339 , GRCh38.p12 chr5: 26,382,001-46,389,237 LOC107986346, RNU6-760P, 227 more genes
    nsv6313844copy number variation1nstd102humanPathogenic GRCh37 chr5: 43,972,062-46,101,844 , GRCh38.p12 chr5: 43,971,960-46,101,742 FGF10, MRPS30, 6 more genes
    nsv6313659copy number variation1nstd102humanPathogenic GRCh37 chr5: 43,855,245-46,389,339 , GRCh38.p12 chr5: 43,855,143-46,389,237 FGF10, MRPS30, 6 more genes
    nsv6312298copy number variation1nstd102humanPathogenic GRCh37 chr5: 42,688,972-44,388,784 , GRCh38.p12 chr5: 42,688,870-44,388,682 LOC100132356, NIM1K, 34 more genes
    nsv6300592copy number variation1nstd186human GRCh37 chr5: 44,401,777-44,402,463 , GRCh38.p12 chr5: 44,401,675-44,402,361 FGF10-AS1
    nsv6135175copy number variation1nstd213human GRCh37 chr5: 29,210,000-46,400,001 , GRCh38.p12 chr5: 29,209,893-46,399,899 CDH6, HMGCS1, 210 more genes
    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
    nsv5458150copy number variation1nstd206human GRCh38 chr5: 44,401,675-44,402,361 , GRCh37.p13 chr5: 44,401,777-44,402,463 FGF10-AS1
    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
    nsv5381519copy number variation1nstd102humanUncertain significance GRCh37 chr5: 44,305,097-45,696,195 , GRCh38.p12 chr5: 44,304,995-45,696,093 HCN1, MRPS30, 5 more genes
    nsv4946950copy number variation1nstd200human GRCh38 chr5: 44,399,643-44,403,832 , GRCh37.p13 chr5: 44,399,745-44,403,934 FGF10-AS1
    nsv4946949copy number variation1nstd200human GRCh38 chr5: 44,393,072-44,396,807 , GRCh37.p13 chr5: 44,393,174-44,396,909 FGF10-AS1
    nsv4802743copy number variation1nstd200human GRCh37 chr5: 44,393,174-44,396,909 , GRCh38.p12 chr5: 44,393,072-44,396,807 FGF10-AS1
    nsv4674231copy number variation1nstd102humanPathogenic GRCh37 chr5: 38,432,180-49,441,945 , GRCh38.p12 chr5: 38,432,078-50,146,111 RPSAP38, LOC105374746, 92 more genes
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