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Items: 1 to 20 of 194

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075642inversion1nstd229human GRCh38 chr13: 74,928,746-75,530,672 , GRCh37.p13 chr13: 75,502,883-76,104,808 CTAGE11P, LOC107984620, 5 more genes
    nsv7068269inversion1nstd229human GRCh38 chr13: 74,964,810-75,272,614 , GRCh37.p13 chr13: 75,538,947-75,846,750 LINC01078, RNU6-38P, 3 more genes
    nsv6950754copy number variation1nstd229human GRCh38 chr13: 75,213,453-75,362,937 , GRCh37.p13 chr13: 75,787,589-75,937,073 LINC01078, CTAGE11P, 1 more genes
    nsv6942174copy number variation1nstd229human GRCh38 chr13: 75,235,191-75,236,664 , GRCh37.p13 chr13: 75,809,327-75,810,800 CTAGE11P
    nsv6638047copy number variation1nstd102humanPathogenic GRCh37 chr13: 75,268,539-115,107,733 , GRCh38.p12 chr13: 74,694,402-114,342,258 CUL4A, LOC105370373, 488 more genes
    nsv6637317copy number variation1nstd102humanUncertain significance GRCh37 chr13: 73,600,015-77,624,907 , GRCh38.p12 chr13: 73,025,877-77,050,772 LOC105370261, BTF3P11, 53 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6492903copy number variation1nstd223human GRCh38 chr13: 73,417,651-75,973,295 , GRCh37.p13 chr13: 73,991,788-76,547,431 SSR1P2, KLF12, 27 more genes
    nsv6485529copy number variation1nstd223human GRCh38 chr13: 75,235,201-75,236,700 , GRCh37.p13 chr13: 75,809,337-75,810,836 CTAGE11P
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314172copy number variation1nstd102humanPathogenic GRCh37 chr13: 75,574,661-87,784,831 , GRCh38.p12 chr13: 75,000,524-87,132,576 LMO7, TBC1D4, 119 more genes
    nsv6314117copy number variation1nstd102humanPathogenic GRCh37 chr13: 36,376,204-80,681,753 , GRCh38.p12 chr13: 35,802,067-80,107,618 RBM26, RNY4P31, 591 more genes
    nsv6314030copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251 RPSAP53, LOC105370213, 1310 more genes
    nsv6291752copy number variation1nstd102humanPathogenic GRCh37 chr13: 59,574,760-89,410,027 , GRCh38.p12 chr13: 59,000,626-88,757,773 GYG1P2, LOC102723968, 284 more genes
    nsv6291487copy number variation1nstd102humanPathogenic GRCh37 chr13: 42,504,540-108,206,269 , GRCh38.p12 chr13: 41,930,404-107,553,921 CALM2P4, RNU6-81P, 778 more genes
    nsv6289999copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 LINC00363, LOC105370118, 1334 more genes
    nsv6132841copy number variation1nstd213human GRCh37 chr13: 67,890,000-75,990,001 , GRCh38.p12 chr13: 67,315,868-75,415,865 KLF5, DACH1, 76 more genes
    nsv6132663copy number variation1nstd213human GRCh37 chr13: 67,680,000-86,760,001 , GRCh38.p12 chr13: 67,105,868-86,185,866 KLF5, BTF3P11, 187 more genes
    nsv5849928copy number variation1nstd209human GRCh38 chr13: 75,235,149-75,236,679 , GRCh37.p13 chr13: 75,809,285-75,810,815 CTAGE11P
    nsv5601667copy number variation1nstd207human GRCh38 chr13: 75,235,117-75,236,674 , GRCh37.p13 chr13: 75,809,253-75,810,810 CTAGE11P
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