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Items: 1 to 20 of 25933

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6137772copy number variation1nstd102humanBenign GRCh38 chr2: 1,493,495-1,493,566 , GRCh37 chr2: 1,497,267-1,497,338 TPO
    nsv6137702copy number variation1nstd102humanPathogenic GRCh37 chr9: 35,059,633-37,660,586 , GRCh38.p12 chr9: 35,059,636-37,660,589 ARHGEF39, LOC105376026, 84 more genes
    nsv6137666copy number variation1nstd102humanPathogenic GRCh37 chrX: 91,829,757-113,050,225 , GRCh38.p12 chrX: 92,574,758-113,806,943 TCEAL8, MTND5P26, 272 more genes
    nsv6131202insertion1nstd186human GRCh37 chr19: 54,402,184-54,402,187 , GRCh38.p12 chr19: 53,898,930-53,898,933 PRKCG
    nsv6131079mobile element insertion1nstd186human GRCh37 chr17: 64,637,294-64,637,345 , GRCh38.p12 chr17: 66,641,176-66,641,227 PRKCA
    nsv6129462insertion1nstd186human GRCh37 chr14: 24,794,428-24,794,428 , GRCh38.p12 chr14: 24,325,222-24,325,222 , GRCh38.p12 chr14|NW_018654722.1: 626,200-626,200 ADCY4
    nsv6127707insertion1nstd186human GRCh37 chr2: 170,036,335-170,036,373 , GRCh38.p12 chr2: 169,179,825-169,179,863 LRP2
    nsv6126556copy number variation1nstd186human GRCh37 chr17: 64,332,752-64,332,805 , GRCh38.p12 chr17: 66,336,634-66,336,687 PRKCA
    nsv6125378insertion1nstd186human GRCh37 chr12: 26,650,425-26,650,472 , GRCh38.p12 chr12: 26,497,492-26,497,539 ITPR2
    nsv6125316copy number variation1nstd186human GRCh37 chr19: 42,495,927-42,496,218 , GRCh38.p12 chr19: 41,991,775-41,992,066 ATP1A3
    nsv6124825insertion1nstd186human GRCh37 chr5: 7,704,113-7,704,113 , GRCh38.p12 chr5: 7,704,000-7,704,000 ADCY2
    nsv6121448copy number variation1nstd186human GRCh37 chr14: 81,469,147-81,469,427 , GRCh38.p12 chr14: 81,002,803-81,003,083 TSHR
    nsv6121447copy number variation1nstd186human GRCh37 chr16: 24,070,222-24,070,272 , GRCh38.p12 chr16: 24,058,901-24,058,951 PRKCB
    nsv6121419copy number variation1nstd186human GRCh37 chr14: 81,597,053-81,597,359 , GRCh38.p12 chr14: 81,130,709-81,131,015 LOC101928462, TSHR
    nsv6121261copy number variation1nstd186human GRCh37 chr14: 81,539,095-81,539,387 , GRCh38.p12 chr14: 81,072,751-81,073,043 LOC101928462, TSHR
    nsv6120126copy number variation1nstd186human GRCh37 chr2: 1,460,465-1,460,739 , GRCh38.p12 chr2: 1,456,693-1,456,967 TPO
    nsv6117042mobile element insertion1nstd186human GRCh37 chr20: 8,816,491-8,816,491 , GRCh38.p12 chr20: 8,835,844-8,835,844 PLCB1
    nsv6116909mobile element insertion1nstd186human GRCh37 chr20: 8,521,304-8,521,355 , GRCh38.p12 chr20: 8,540,657-8,540,708 PLCB1
    nsv6116900copy number variation1nstd186human GRCh37 chr17: 64,794,356-64,795,702 , GRCh38.p12 chr17: 66,798,238-66,799,584 PRKCA
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