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Items: 1 to 20 of 1692

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112761copy number variation1nstd102humanPathogenic GRCh37 chr4: 69,671-29,702,595 , GRCh38.p12 chr4: 69,779-29,700,973 LOC101928306, PDE6B-AS1, 460 more genes
    nsv5964987insertion1nstd209human GRCh38 chr4: 23,974,799-23,974,799 , GRCh37.p13 chr4: 23,976,422-23,976,422 PPARGC1A
    nsv5959319insertion1nstd209human GRCh38 chr4: 24,125,005-24,125,005 , GRCh37.p13 chr4: 24,126,628-24,126,628 PPARGC1A
    nsv5957961insertion1nstd209human GRCh38 chr4: 24,467,007-24,467,007 , GRCh37.p13 chr4: 24,468,630-24,468,630 PPARGC1A
    nsv5950637insertion1nstd209human GRCh38 chr4: 24,229,152-24,229,152 , GRCh37.p13 chr4: 24,230,775-24,230,775 PPARGC1A
    nsv5949787insertion1nstd209human GRCh38 chr4: 23,871,193-23,871,193 , GRCh37.p13 chr4: 23,872,816-23,872,816 PPARGC1A
    nsv5948575insertion1nstd209human GRCh38 chr4: 23,919,667-23,919,667 , GRCh37.p13 chr4: 23,921,290-23,921,290 PPARGC1A
    nsv5906067copy number variation1nstd209human GRCh38 chr4: 22,920,705-27,042,181 , GRCh37.p13 chr4: 22,922,328-27,043,803 , SEPSECS, 49 more genes
    nsv5905316copy number variation1nstd209human GRCh38 chr4: 24,346,728-24,346,903 , GRCh37.p13 chr4: 24,348,351-24,348,526 PPARGC1A
    nsv5904817copy number variation1nstd209human GRCh38 chr4: 24,086,255-24,088,690 , GRCh37.p13 chr4: 24,087,878-24,090,313 PPARGC1A
    nsv5904605copy number variation1nstd209human GRCh38 chr4: 24,271,079-24,271,156 , GRCh37.p13 chr4: 24,272,702-24,272,779 PPARGC1A
    nsv5902659copy number variation1nstd209human GRCh38 chr4: 23,918,796-23,919,002 , GRCh37.p13 chr4: 23,920,419-23,920,625 PPARGC1A
    nsv5902421copy number variation1nstd209human GRCh38 chr4: 24,212,996-24,213,094 , GRCh37.p13 chr4: 24,214,619-24,214,717 PPARGC1A
    nsv5897619copy number variation1nstd209human GRCh38 chr4: 23,951,198-23,952,576 , GRCh37.p13 chr4: 23,952,821-23,954,199 PPARGC1A
    nsv5894283copy number variation1nstd209human GRCh38 chr4: 24,025,658-24,025,721 , GRCh37.p13 chr4: 24,027,281-24,027,344 PPARGC1A
    nsv5892971copy number variation1nstd209human GRCh38 chr4: 23,909,434-23,910,243 , GRCh37.p13 chr4: 23,911,057-23,911,866 PPARGC1A
    nsv5892881copy number variation1nstd209human GRCh38 chr4: 24,101,868-24,101,921 , GRCh37.p13 chr4: 24,103,491-24,103,544 PPARGC1A
    nsv5890270copy number variation1nstd209human GRCh38 chr4: 23,918,717-23,918,782 , GRCh37.p13 chr4: 23,920,340-23,920,405 PPARGC1A
    nsv5887890copy number variation1nstd209human GRCh38 chr4: 24,188,151-24,190,241 , GRCh37.p13 chr4: 24,189,774-24,191,864 PPARGC1A
    nsv5839227copy number variation1nstd209human GRCh38 chr4: 24,323,565-24,328,107 , GRCh37.p13 chr4: 24,325,188-24,329,730 PPARGC1A
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