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Items: 1 to 20 of 316

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5905243copy number variation1nstd209human GRCh38 chr2: 203,257,939-203,257,988 , GRCh37.p13 chr2: 204,122,662-204,122,711 RN7SL670P, CYP20A1
    nsv5898262copy number variation1nstd209human GRCh38 chr2: 203,298,929-203,302,877 , GRCh37.p13 chr2: 204,163,652-204,167,600 CYP20A1
    nsv5832374copy number variation1nstd209human GRCh38 chr2: 203,299,261-203,302,915 , GRCh37.p13 chr2: 204,163,984-204,167,638 CYP20A1
    nsv5718781mobile element insertion1nstd211human GRCh38 chr2: 203,296,921-203,296,921 , GRCh37.p13 chr2: 204,161,644-204,161,644 CYP20A1
    nsv5619211insertion1nstd207human GRCh38 chr2: 203,251,793-203,251,793 , GRCh37.p13 chr2: 204,116,516-204,116,516 CYP20A1
    nsv5614959insertion2nstd207human GRCh38 chr2: 203,257,939-203,257,939 , GRCh37.p13 chr2: 204,122,662-204,122,662 RN7SL670P, CYP20A1
    nsv5605159insertion1nstd207human GRCh38 chr2: 203,251,815-203,251,815 , GRCh37.p13 chr2: 204,116,538-204,116,538 CYP20A1
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5446906copy number variation1nstd206human GRCh38 chr2: 203,263,238-203,265,045 , GRCh37.p13 chr2: 204,127,961-204,129,768 CYP20A1
    nsv5443068copy number variation1nstd206human GRCh38 chr2: 203,306,142-203,310,085 , GRCh37.p13 chr2: 204,170,865-204,174,808 CYP20A1
    nsv5439962copy number variation1nstd206human GRCh38 chr2: 203,247,025-203,248,279 , GRCh37.p13 chr2: 204,111,748-204,113,002 CYP20A1
    nsv5433981copy number variation1nstd206human GRCh38 chr2: 203,297,784-203,298,692 , GRCh37.p13 chr2: 204,162,507-204,163,415 CYP20A1
    nsv5340573translocation1nstd200human GRCh37 chr2: 204,164,845-204,164,845 , GRCh37 chr5: 87,681,276-87,681,276 , GRCh38.p12 chr2: 203,300,122-203,300,122 , GRCh38.p12 chr5: 88,385,459-88,385,459 TMEM161B-DT, CYP20A1
    nsv5309113copy number variation1nstd204human GRCh38.p13 chr2: 203,306,137-203,310,094 , GRCh37.p13 chr2: 204,170,860-204,174,817 CYP20A1
    nsv5307820copy number variation1nstd204human GRCh38.p13 chr2: 203,275,693-203,290,941 , GRCh37.p13 chr2: 204,140,416-204,155,664 CYP20A1
    nsv5218252copy number variation1nstd204human GRCh38.p13 chr2: 203,306,016-203,309,150 , GRCh37.p13 chr2: 204,170,739-204,173,873 CYP20A1
    nsv5202889copy number variation1nstd204human GRCh38.p13 chr2: 203,306,201-203,310,100 , GRCh37.p13 chr2: 204,170,924-204,174,823 CYP20A1
    nsv5202286copy number variation1nstd204human GRCh38.p13 chr2: 203,275,559-203,289,731 , GRCh37.p13 chr2: 204,140,282-204,154,454 CYP20A1
    nsv5076214mobile element insertion1nstd203human GRCh38 chr2: 203,300,518-203,300,533 , GRCh37.p13 chr2: 204,165,241-204,165,256 CYP20A1
    nsv5070230mobile element insertion1nstd203human GRCh38 chr2: 203,267,940-203,267,953 , GRCh37.p13 chr2: 204,132,663-204,132,676 CYP20A1
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