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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5943805copy number variation1nstd209human GRCh38 chr14: 44,504,920-44,505,063 , GRCh37.p13 chr14: 44,974,123-44,974,266 FSCB
    nsv5940619copy number variation1nstd209human GRCh38 chr14: 41,756,659-48,371,099 , GRCh37.p13 chr14: 42,225,862-48,840,302 LOC100418768, RNU6-297P, 53 more genes
    nsv5853242copy number variation1nstd209human GRCh38 chr14: 44,490,798-44,524,243 , GRCh37.p13 chr14: 44,960,001-44,993,446 FSCB, LOC105370473
    nsv5849917copy number variation1nstd209human GRCh38 chr14: 44,457,480-44,505,163 , GRCh37.p13 chr14: 44,926,683-44,974,366 LINC02277, FSCB
    nsv5652172insertion1nstd207human GRCh38 chr14: 44,504,951-44,504,951 , GRCh37.p13 chr14: 44,974,154-44,974,154 FSCB
    nsv5586915copy number variation1nstd207human GRCh38 chr14: 44,504,920-44,504,991 , GRCh37.p13 chr14: 44,974,123-44,974,194 FSCB
    nsv5502760copy number variation1nstd206human GRCh38 chr14: 44,504,171-44,504,259 , GRCh37.p13 chr14: 44,973,374-44,973,462 FSCB
    nsv5357170translocation1nstd200human GRCh38 chr14: 44,504,259-44,504,259 , GRCh38 chr14: 44,504,171-44,504,171 , GRCh37.p13 chr14: 44,973,374-44,973,374 , GRCh37.p13 chr14: 44,973,462-44,973,462 FSCB
    nsv4844259copy number variation1nstd200human GRCh37 chr14: 43,998,688-46,847,593 , GRCh38.p12 chr14: 43,529,485-46,378,390 RNU6-552P, C14orf28, 32 more genes
    nsv4842647copy number variation1nstd200human GRCh37 chr14: 44,973,374-44,973,462 , GRCh38.p12 chr14: 44,504,171-44,504,259 FSCB
    nsv4767727insertion1nstd199human GRCh37 chr14: 44,974,188-44,974,188 , GRCh38.p12 chr14: 44,504,985-44,504,985 FSCB
    nsv4729533copy number variation1nstd102humanLikely benign GRCh37 chr14: 44,556,606-44,984,689 , GRCh38.p12 chr14: 44,087,403-44,515,486 YWHAZP1, LOC645086, 3 more genes
    nsv4675104copy number variation1nstd102humanLikely benign GRCh37 chr14: 44,750,751-45,024,841 , GRCh38.p12 chr14: 44,281,548-44,555,638 FSCB, YWHAZP1, 2 more genes
    nsv4629220copy number variation1nstd183human GRCh37 chr14: 43,856,759-45,407,050 , GRCh38.p12 chr14: 43,387,556-44,937,847 KRT8P2, LOC401770, 15 more genes
    nsv4413839copy number variation1nstd174human GRCh37 chr14: 43,691,752-45,412,080 , GRCh38.p12 chr14: 43,222,549-44,942,877 LINC02302, KLHL28, 18 more genes
    nsv4388388copy number variation1nstd173human GRCh37 chr14: 44,939,853-45,011,772 , GRCh38.p12 chr14: 44,470,650-44,542,569 LINC02277, FSCB, 1 more genes
    nsv4377555copy number variation1nstd173human GRCh37 chr14: 44,939,853-45,004,380 , GRCh38.p12 chr14: 44,470,650-44,535,177 LOC105370473, FSCB, 1 more genes
    nsv4368733copy number variation1nstd173human GRCh37 chr14: 44,939,853-45,004,449 , GRCh38.p12 chr14: 44,470,650-44,535,246 LINC02277, FSCB, 1 more genes
    nsv4230636copy number variation1nstd166human GRCh37.p13 chr14: 44,893,110-45,142,956 , GRCh38.p12 chr14: 44,423,907-44,673,753 LOC105370472, FSCB, 2 more genes
    nsv4220558copy number variation1nstd166human GRCh37.p13 chr14: 44,973,374-44,973,462 , GRCh38.p12 chr14: 44,504,171-44,504,259 FSCB
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