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Items: 1 to 20 of 121

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139252insertion1nstd232human GRCh37.p13 chr5: 43,292,747-43,292,747 , GRCh38.p12 chr5: 43,292,645-43,292,645 HMGCS1
    nsv6774697copy number variation1nstd229human GRCh38 chr5: 43,312,001-43,385,400 , GRCh37.p13 chr5: 43,312,103-43,385,502 CCL28, HMGCS1, 1 more genes
    nsv6767368copy number variation1nstd229human GRCh38 chr5: 43,281,116-43,944,609 , GRCh37.p13 chr5: 43,281,218-43,944,711 TMEM267, C5orf34-AS1, 11 more genes
    nsv6764190copy number variation1nstd229human GRCh38 chr5: 43,285,915-43,286,048 , GRCh37.p13 chr5: 43,286,017-43,286,150 HMGCS1
    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
    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
    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
    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
    nsv6300383copy number variation1nstd186human GRCh37 chr5: 26,834,087-43,674,516 , GRCh38.p12 chr5: 26,833,978-43,674,414 , TMEM267, 221 more genes
    nsv6136117copy number variation1nstd213human GRCh37 chr5: 41,590,000-44,160,001 , GRCh38.p12 chr5: 41,589,898-44,159,899 GHR, OXCT1, 44 more genes
    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
    nsv6135152copy number variation1nstd213human GRCh37 chr5: 38,620,000-43,420,001 , GRCh38.p12 chr5: 38,619,898-43,419,899 C6, C9, 70 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
    nsv5628011insertion1nstd207human GRCh38 chr5: 43,285,915-43,285,915 , GRCh37.p13 chr5: 43,286,017-43,286,017 HMGCS1
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5462914copy number variation1nstd206human GRCh38 chr5: 43,285,915-43,286,066 , GRCh37.p13 chr5: 43,286,017-43,286,168 HMGCS1
    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
    nsv5368244translocation1nstd200human GRCh38 chr5: 43,288,857-43,288,857 , GRCh38 chr5: 43,288,920-43,288,920 , GRCh37.p13 chr5: 43,289,022-43,289,022 , GRCh37.p13 chr5: 43,288,959-43,288,959 HMGCS1
    nsv5093530mobile element insertion1nstd203human GRCh38 chr5: 43,288,669-43,288,681 , GRCh37.p13 chr5: 43,288,771-43,288,783 HMGCS1
    nsv4944648copy number variation1nstd200human GRCh38 chr5: 43,313,883-43,339,898 , GRCh37.p13 chr5: 43,313,985-43,340,000 HMGCS1
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