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Items: 1 to 20 of 156

  • The following term was not found in dbVar: 06281355.
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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6141130copy number variation1nstd206human GRCh38 chr4: 73,982,179-73,982,236 , GRCh37.p13 chr4: 74,847,896-74,847,953 PF4
    nsv6295235copy number variation1nstd186human GRCh37 chr4: 74,847,896-74,847,953 , GRCh38.p12 chr4: 73,982,179-73,982,236 PF4
    nsv5998095copy number variation1nstd212human GRCh38 chr4: 73,982,164-73,982,233 , GRCh37.p13 chr4: 74,847,881-74,847,950 PF4
    nsv4096579copy number variation1nstd166human GRCh37.p13 chr4: 74,847,896-74,847,953 , GRCh38.p12 chr4: 73,982,179-73,982,236 PF4
    esv1503583copy number variation1estd22human NCBI36 chr4: 75,066,768-75,066,790 , GRCh37.p13 chr4: 74,847,904-74,847,926 , GRCh38.p12 chr4: 73,982,187-73,982,209 PF4
    nsv5090896mobile element insertion1nstd203human GRCh38 chr4: 73,982,164-73,982,209 , GRCh37.p13 chr4: 74,847,881-74,847,926 PF4
    nsv5089346mobile element insertion1nstd203human GRCh38 chr4: 73,982,209-73,982,209 , GRCh37.p13 chr4: 74,847,926-74,847,926 PF4
    esv2422526insertion1estd197human NCBI36 chr4: 75,065,330-75,065,330 , GRCh37.p13 chr4: 74,846,466-74,846,466 , GRCh38.p12 chr4: 73,980,749-73,980,749 PF4
    esv2338149insertion1estd194human NCBI36 chr4: 75,065,324-75,065,324 , GRCh37.p13 chr4: 74,846,460-74,846,460 , GRCh38.p12 chr4: 73,980,743-73,980,743 PF4
    nsv5839480copy number variation1nstd209human GRCh38 chr4: 73,982,086-73,985,847 , GRCh37.p13 chr4: 74,847,803-74,851,564 PPBP, PF4
    nsv7038209inversion1nstd229human GRCh38 chr4: 73,862,232-73,981,191 , GRCh37.p13 chr4: 74,727,949-74,846,908 HNRNPA1P55, PF4, 2 more genes
    nsv6567979inversion1nstd223human GRCh38 chr4: 73,853,793-73,981,533 , GRCh37.p13 chr4: 74,719,510-74,847,250 CXCL1, PF4, 3 more genes
    nsv5559067sequence alteration1nstd206human GRCh38 chr4: 73,853,806-73,981,615 , GRCh37.p13 chr4: 74,719,523-74,847,332 CXCL1, PF4, 3 more genes
    nsv3923759copy number variation1nstd102humanPathogenic NCBI36 chr4: 58,862,002-102,129,682 , GRCh37.p13 chr4: 59,167,245-101,910,659 , GRCh38.p12 chr4: 58,301,079-100,989,502 EREG, EFL1P2, 530 more genes
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv4729598copy number variation1nstd102humanPathogenic GRCh37 chr4: 71,412,409-87,920,784 , GRCh38.p12 chr4: 70,546,692-86,999,632 PTPN11P5, LOC643014, 244 more genes
    nsv6314916copy number variation1nstd102humanPathogenic GRCh38 chr4: 67,833,055-82,716,065 , GRCh37.p13 chr4: 68,698,773-83,637,218 MICOS10P4, SULT1B1, 274 more genes
    nsv4674589copy number variation1nstd102humanPathogenic GRCh37 chr4: 72,680,879-86,426,232 , GRCh38.p12 chr4: 71,815,162-85,505,079 SOWAHB, FTLP9, 211 more genes
    nsv4674141copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,950,363-79,738,598 , GRCh38.p12 chr4: 68,084,645-78,817,444 COX18, UGT2B11, 216 more genes
    nsv3884502copy number variation1nstd102humanPathogenic GRCh37 chr4: 66,017,575-76,772,947 , GRCh38.p12 chr4: 65,151,857-75,851,794 RNU2-40P, CDKL2, 188 more genes
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