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Items: 1 to 20 of 564

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6876025copy number variation1nstd229human GRCh38 chr9: 39,096,070-39,096,295 , GRCh37.p13 chr9: 39,096,067-39,096,292 CNTNAP3
    nsv6873816copy number variation1nstd229human GRCh38 chr9: 39,108,311-39,132,024 , GRCh37.p13 chr9: 39,108,308-39,132,021 CNTNAP3
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6634409copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 1-40,036,525 , GRCh38.p12 chr9: 10,001-39,445,729 ACO1, PLIN2, 594 more genes
    nsv6633995copy number variation2nstd224human GRCh37 chr9: 39,021,035-39,167,367 , GRCh38.p12 chr9: 39,021,038-39,167,370 CNTNAP3, RBM17P1, 1 more genes
    nsv6633994copy number variation6nstd224human GRCh37 chr9: 39,004,140-39,154,913 , GRCh38.p12 chr9: 39,004,143-39,154,916 CNTNAP3, RBM17P1, 1 more genes
    nsv6633993copy number variation2nstd224human GRCh37 chr9: 38,808,947-39,154,913 , GRCh38.p12 chr9: 38,808,950-39,154,916 CNTNAP3, VN2R3P, 4 more genes
    nsv6633909copy number variation6nstd224human GRCh37 chr9: 39,098,698-39,154,913 , GRCh38.p12 chr9: 39,098,701-39,154,916 RBM17P1, CNTNAP3
    nsv6633908copy number variation1nstd224human GRCh37 chr9: 39,021,035-39,297,857 , GRCh38.p12 chr9: 39,021,038-39,297,860 CNTNAP3, VN2R3P, 3 more genes
    nsv6633907copy number variation5nstd224human GRCh37 chr9: 39,004,140-39,103,743 , GRCh38.p12 chr9: 39,004,143-39,103,746 CNTNAP3, VN2R3P
    nsv6633523copy number variation1nstd224human GRCh37 chr9: 39,021,035-39,180,169 , GRCh38.p12 chr9: 39,021,038-39,180,172 RBM17P1, CNTNAP3, 1 more genes
    nsv6633522copy number variation2nstd224human GRCh37 chr9: 39,021,035-39,140,153 , GRCh38.p12 chr9: 39,021,038-39,140,156 CNTNAP3, VN2R3P
    nsv6633521copy number variation2nstd224human GRCh37 chr9: 39,019,085-39,154,913 , GRCh38.p12 chr9: 39,019,088-39,154,916 VN2R3P, CNTNAP3, 1 more genes
    nsv6633520copy number variation9nstd224human GRCh37 chr9: 39,004,140-39,151,736 , GRCh38.p12 chr9: 39,004,143-39,151,739 CNTNAP3, VN2R3P
    nsv6573618inversion1nstd223human GRCh38 chr9: 39,067,449-39,068,345 , GRCh37.p13 chr9: 39,067,446-39,068,342 CNTNAP3
    nsv6450659copy number variation1nstd223human GRCh38 chr9: 39,080,301-39,081,100 , GRCh37.p13 chr9: 39,080,298-39,081,097 CNTNAP3
    nsv6450354copy number variation1nstd223human GRCh38 chr9: 39,096,070-39,096,295 , GRCh37.p13 chr9: 39,096,067-39,096,292 CNTNAP3
    nsv6446499copy number variation1nstd223human GRCh38 chr9: 39,082,501-39,149,800 , GRCh37.p13 chr9: 39,082,498-39,149,797 CNTNAP3
    nsv6444355copy number variation1nstd223human GRCh38 chr9: 39,072,801-39,124,800 , GRCh37.p13 chr9: 39,072,798-39,124,797 CNTNAP3
    nsv6443908copy number variation1nstd223human GRCh38 chr9: 39,125,801-39,127,600 , GRCh37.p13 chr9: 39,125,798-39,127,597 CNTNAP3
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