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Items: 1 to 20 of 166705

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137713insertion1nstd102humanUncertain significance GRCh37 chr18: 48,581,368-48,581,368 , GRCh38 chr18: 51,054,998-51,054,998 SMAD4
    nsv6137708copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 42,981,187-42,987,120 , GRCh38.p12 chr20: 44,352,547-44,358,480 HNF4A, R3HDML-AS1
    nsv6137707copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,565,626-30,221,925 , GRCh38.p12 chr16: 29,554,305-30,210,604 ZG16, TBX6, 45 more genes
    nsv6137705copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,419,493-40,774,118 , GRCh38.p12 chr9: 36,419,496-39,445,729 , GRCh38.p12 chr9: 61,281,967-67,217,006 LOC107987010, LOC107987007, 218 more genes
    nsv6137672copy number variation1nstd102humannot provided GRCh38 chr2: 124,348,648-129,410,245 , GRCh37.p13 chr2: 125,106,225-130,167,818 ERCC3, MYO7B, 59 more genes
    nsv6137671copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 41,251,504-41,251,866 , GRCh38 chr17: 43,099,487-43,099,849 BRCA1
    nsv6137666copy number variation1nstd102humanPathogenic GRCh37 chrX: 91,829,757-113,050,225 , GRCh38.p12 chrX: 92,574,758-113,806,943 RPSAP8, HNRNPA1P26, 275 more genes
    nsv6131680insertion1nstd186human GRCh37 chr16: 2,102,234-2,102,266 , GRCh38.p12 chr16: 2,052,233-2,052,265 TSC2
    nsv6131612insertion1nstd186human GRCh37 chr12: 133,512,225-133,512,225 , GRCh38.p12 chr12: 132,935,639-132,935,639 ZNF605
    nsv6131611insertion1nstd186human GRCh37 chr19: 14,841,278-14,841,322 , GRCh38.p12 chr19: 14,730,466-14,730,510 ZNF333, ADGRE2
    nsv6131517mobile element insertion1nstd186human GRCh37 chr6: 45,325,836-45,325,887 , GRCh38.p12 chr6: 45,358,099-45,358,150 SUPT3H, RUNX2
    nsv6131489insertion1nstd186human GRCh37 chr12: 124,818,574-124,818,586 , GRCh38.p12 chr12: 124,334,028-124,334,040 NCOR2
    nsv6131471insertion1nstd186human GRCh37 chr13: 45,799,552-45,799,603 , GRCh38.p12 chr13: 45,225,417-45,225,468 GTF2F2, LOC105370190
    nsv6131369insertion1nstd186human GRCh37 chr14: 102,316,011-102,316,011 , GRCh38.p12 chr14: 101,849,674-101,849,674 PPP2R5C
    nsv6131360mobile element insertion1nstd186human GRCh37 chr4: 146,749-146,800 , GRCh38.p12 chr4: 152,970-153,021 ZNF718
    nsv6131338insertion1nstd186human GRCh37 chr19: 22,373,464-22,373,500 , GRCh38.p12 chr19|NW_003315965.1: 118,176-118,212 , GRCh38.p12 chr19: 22,190,662-22,190,698 ZNF676
    nsv6131306insertion1nstd186human GRCh37 chr20: 35,698,248-35,698,248 , GRCh38.p12 chr20: 37,069,845-37,069,845 RBL1
    nsv6131298insertion1nstd186human GRCh37 chr19: 36,686,550-36,686,550 , GRCh38.p12 chr19: 36,195,648-36,195,648 ZNF565
    nsv6131290mobile element insertion1nstd186human GRCh37 chr3: 20,090,533-20,090,584 , GRCh38.p12 chr3: 20,049,041-20,049,092 KAT2B
    nsv6131287insertion1nstd186human GRCh37 chr19: 21,285,990-21,285,990 , GRCh38.p12 chr19: 21,103,184-21,103,184 ZNF714
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