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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3137683copy number variation1nstd151human GRCh37 (hg19) chr2: 6,989,978-12,880,925 , GRCh38 (hg38) chr2: 6,849,847-12,740,799 CPSF3, KCNF1, 115 more genes
    nsv3128832copy number variation1nstd151human GRCh37 (hg19) chr2: 8,822,293-12,880,925 , GRCh38 (hg38) chr2: 8,682,163-12,740,799 CPSF3, ID2, 90 more genes
    nsv3109819copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr2: 12,770-20,081,474 , GRCh38 (hg38) chr2: 12,770-19,881,713 , NCBI36 (hg18) chr2: 2,770-19,944,955 CPSF3, DDX1, 257 more genes
    nsv3080669mobile element insertion2nstd144human GRCh37 (hg19) chr2: 9,566,759-9,566,759 , GRCh38 (hg38) chr2: 9,426,630-9,426,630 CPSF3
    nsv3080378mobile element insertion1nstd144human GRCh37 (hg19) chr2: 9,591,111-9,591,111 , GRCh38 (hg38) chr2: 9,450,982-9,450,982 CPSF3
    nsv2776363copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr2: 12,771-242,783,384 , GRCh38 (hg38) chr2: 12,771-241,841,232 , NCBI36 (hg18) chr2: 2,771-242,432,057 CPSF3, MIR561, 3855 more genes
    esv3823175mobile element insertion1estd219human GRCh37 (hg19) chr2: 9,591,111-9,591,111 , GRCh38 (hg38) chr2: 9,450,982-9,450,982 CPSF3
    esv3823176copy number variation10estd219human GRCh37 (hg19) chr2: 9,601,644-9,603,426 , GRCh38 (hg38) chr2: 9,461,515-9,463,297 CPSF3
    esv3823174mobile element insertion1estd219human GRCh37 (hg19) chr2: 9,566,759-9,566,759 , GRCh38 (hg38) chr2: 9,426,630-9,426,630 CPSF3
    nsv2070309short tandem repeat2nstd128human GRCh37 (hg19) chr2: 9,606,725-9,606,745 , GRCh38 (hg38) chr2: 9,466,596-9,466,616 CPSF3
    nsv2070306short tandem repeat11nstd128human GRCh37 (hg19) chr2: 9,606,470-9,606,482 , GRCh38 (hg38) chr2: 9,466,341-9,466,353 CPSF3
    nsv2070302short tandem repeat6nstd128human GRCh37 (hg19) chr2: 9,606,305-9,606,362 , GRCh38 (hg38) chr2: 9,466,176-9,466,233 CPSF3
    nsv2070298short tandem repeat2nstd128human GRCh37 (hg19) chr2: 9,606,001-9,606,016 , GRCh38 (hg38) chr2: 9,465,872-9,465,887 CPSF3
    nsv2070294short tandem repeat6nstd128human GRCh37 (hg19) chr2: 9,605,672-9,605,693 , GRCh38 (hg38) chr2: 9,465,543-9,465,564 CPSF3
    nsv2070290short tandem repeat1nstd128human GRCh37 (hg19) chr2: 9,604,709-9,604,738 , GRCh38 (hg38) chr2: 9,464,580-9,464,609 CPSF3
    nsv2070282short tandem repeat1nstd128human GRCh37 (hg19) chr2: 9,601,799-9,601,809 , GRCh38 (hg38) chr2: 9,461,670-9,461,680 CPSF3
    nsv2070267short tandem repeat16nstd128human GRCh37 (hg19) chr2: 9,597,277-9,597,320 , GRCh38 (hg38) chr2: 9,457,148-9,457,191 CPSF3
    nsv2070264short tandem repeat1nstd128human GRCh37 (hg19) chr2: 9,595,887-9,595,898 , GRCh38 (hg38) chr2: 9,455,758-9,455,769 CPSF3
    nsv2070244short tandem repeat1nstd128human GRCh37 (hg19) chr2: 9,589,346-9,589,367 , GRCh38 (hg38) chr2: 9,449,217-9,449,238 CPSF3
    nsv2070239short tandem repeat3nstd128human GRCh37 (hg19) chr2: 9,584,754-9,584,813 , GRCh38 (hg38) chr2: 9,444,625-9,444,684 CPSF3
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