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Items: 1 to 20 of 358

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094476copy number variation1nstd102humanPathogenic GRCh37 chr13: 37,446,775-37,453,826 , GRCh38.p12 chr13: 36,872,638-36,879,689 SMAD9
    nsv7058180inversion1nstd229human GRCh38 chr13: 29,278,598-37,954,955 , GRCh37.p13 chr13: 29,852,735-38,529,092 ZAR1L, HSPH1, 116 more genes
    nsv6957553copy number variation1nstd229human GRCh38 chr13: 36,871,210-36,881,422 , GRCh37.p13 chr13: 37,445,347-37,455,559 SMAD9
    nsv6956961copy number variation1nstd229human GRCh38 chr13: 36,731,812-37,044,306 , GRCh37.p13 chr13: 37,305,949-37,618,443 GAPDHP34, SMAD9, 11 more genes
    nsv6954038copy number variation1nstd229human GRCh38 chr13: 36,860,361-36,861,735 , GRCh37.p13 chr13: 37,434,498-37,435,872 SMAD9
    nsv6952772copy number variation1nstd229human GRCh38 chr13: 36,780,329-36,844,248 , GRCh37.p13 chr13: 37,354,466-37,418,385 LOC102723490, NDE1P2, 3 more genes
    nsv6952302copy number variation1nstd229human GRCh38 chr13: 36,864,591-37,014,980 , GRCh37.p13 chr13: 37,438,728-37,589,117 EXOSC8, ALG5, 5 more genes
    nsv6951807copy number variation1nstd229human GRCh38 chr13: 36,854,010-36,861,638 , GRCh37.p13 chr13: 37,428,147-37,435,775 SMAD9
    nsv6951403copy number variation1nstd229human GRCh38 chr13: 36,667,941-36,850,506 , GRCh37.p13 chr13: 37,242,078-37,424,643 SERTM1, RFXAP, 6 more genes
    nsv6947862copy number variation1nstd229human GRCh38 chr13: 36,879,574-36,882,595 , GRCh37.p13 chr13: 37,453,711-37,456,732 SMAD9
    nsv6945398copy number variation1nstd229human GRCh38 chr13: 36,829,501-36,865,800 , GRCh37.p13 chr13: 37,403,638-37,439,937 SMAD9, RFXAP
    nsv6944772copy number variation1nstd229human GRCh38 chr13: 36,881,046-36,906,473 , GRCh37.p13 chr13: 37,455,183-37,480,610 SMAD9
    nsv6943168copy number variation1nstd229human GRCh38 chr13: 36,839,070-36,848,100 , GRCh37.p13 chr13: 37,413,207-37,422,237 SMAD9
    nsv6942326copy number variation1nstd229human GRCh38 chr13: 36,882,494-36,883,149 , GRCh37.p13 chr13: 37,456,631-37,457,286 SMAD9
    nsv6939971copy number variation1nstd229human GRCh38 chr13: 36,918,958-36,940,234 , GRCh37.p13 chr13: 37,493,095-37,514,371 SMAD9, RPL29P28, 2 more genes
    nsv6637985copy number variation1nstd102humanUncertain significance GRCh37 chr13: 36,148,057-41,670,428 , GRCh38.p12 chr13: 35,573,920-41,096,292 RPS12P24, SPART, 86 more genes
    nsv6637238copy number variation1nstd102humanPathogenic GRCh37 chr13: 35,501,428-40,901,176 , GRCh38.p12 chr13: 34,927,291-40,327,039 CCDC169-SOHLH2, RNA5SP26, 74 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
    nsv6589616inversion1nstd223human GRCh38 chr13: 36,859,956-36,860,742 , GRCh37.p13 chr13: 37,434,093-37,434,879 SMAD9
    nsv6584172inversion1nstd223human GRCh38 chr13: 36,854,030-36,854,671 , GRCh37.p13 chr13: 37,428,167-37,428,808 SMAD9
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