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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3138202copy number variation6nstd151human GRCh37 (hg19) chr4: 17,805,111-17,819,716 , GRCh38 (hg38) chr4: 17,803,488-17,818,093 DCAF16, NCAPG
    nsv2777044copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr4: 68,345-20,533,787 , GRCh38 (hg38) chr4: 68,453-20,532,164 , NCBI36 (hg18) chr4: 58,345-20,142,885 MIR943, DEFB108F, 193 more genes
    nsv2775460copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr4: 68,345-49,089,361 , GRCh38 (hg38) chr4: 68,453-49,087,344 , NCBI36 (hg18) chr4: 58,345-48,784,118 MIR943, DEFB108F, 314 more genes
    nsv2773415copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr4: 68,345-49,093,788 , GRCh38 (hg38) chr4: 68,453-49,091,771 , NCBI36 (hg18) chr4: 58,345-48,788,545 MIR943, DEFB108F, 314 more genes
    nsv2773339copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr4: 12,440-190,904,441 , GRCh38 (hg38) chr4: 12,440-189,983,286 , NCBI36 (hg18) chr4: 2,440-191,141,435 SNHG8, MIR943, 1039 more genes
    nsv2772184copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr4: 16,826,659-17,818,949 , GRCh38 (hg38) chr4: 16,825,036-17,817,326 , NCBI36 (hg18) chr4: 16,435,757-17,428,047 LINC02493, FAM184B, 7 more genes
    nsv2769771copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr4: 68,345-66,440,622 , GRCh38 (hg38) chr4: 68,453-65,574,904 , NCBI36 (hg18) chr4: 58,345-66,123,217 MIR943, DEFB108F, 375 more genes
    nsv2769375copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr4: 68,346-190,957,473 , GRCh38 (hg38) chr4: 68,454-190,036,318 , NCBI36 (hg18) chr4: 58,346-191,194,467 SNHG8, MIR943, 1041 more genes
    nsv2735207copy number variation1nstd130human NCBI36 (hg18) chr4: 17,300,145-17,457,027 , GRCh37 (hg19) chr4: 17,691,047-17,847,929 , GRCh38 (hg38) chr4: 17,689,424-17,846,306 LCORL, FAM184B, 2 more genes
    nsv2316781short tandem repeat4nstd128human GRCh37 (hg19) chr4: 17,810,223-17,810,245 , GRCh38 (hg38) chr4: 17,808,600-17,808,622 DCAF16
    nsv2316778short tandem repeat1nstd128human GRCh37 (hg19) chr4: 17,807,590-17,807,604 , GRCh38 (hg38) chr4: 17,805,967-17,805,981 DCAF16
    nsv2292199short tandem repeat3nstd128human GRCh37 (hg19) chr4: 17,802,760-17,802,771 , GRCh38 (hg38) chr4: 17,801,137-17,801,148 DCAF16
    nsv2291776short tandem repeat5nstd128human GRCh37 (hg19) chr4: 17,804,264-17,804,290 , GRCh38 (hg38) chr4: 17,802,641-17,802,667 DCAF16
    nsv2291771short tandem repeat3nstd128human GRCh37 (hg19) chr4: 17,802,477-17,802,491 , GRCh38 (hg38) chr4: 17,800,854-17,800,868 DCAF16
    nsv2291679short tandem repeat9nstd128human GRCh37 (hg19) chr4: 17,806,708-17,806,727 , GRCh38 (hg38) chr4: 17,805,085-17,805,104 DCAF16
    nsv2291676short tandem repeat3nstd128human GRCh37 (hg19) chr4: 17,804,654-17,804,665 , GRCh38 (hg38) chr4: 17,803,031-17,803,042 DCAF16
    nsv2291661short tandem repeat1nstd128human GRCh37 (hg19) chr4: 17,800,230-17,800,246 , GRCh38 (hg38) chr4: 17,798,607-17,798,623 DCAF16
    nsv1398314copy number variation1nstd102humanUncertain significance GRCh37 (hg19) chr4: 16,830,399-17,805,183 , GRCh38 (hg38) chr4: 16,828,776-17,803,560 , NCBI36 (hg18) chr4: 16,439,497-17,414,281 LINC02493, FAM184B, 6 more genes
    nsv1398080copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr4: 44,020-19,796,182 , NCBI36 (hg18) chr4: 34,020-19,405,280 , GRCh38 (hg38) chr4: 44,019-19,794,559 MIR943, DEFB108F, 190 more genes
    esv3893889copy number variation1estd224human NCBI36 (hg18) chr4: 17,418,636-17,428,233 , GRCh37 (hg19) chr4: 17,809,538-17,819,135 , GRCh38 (hg38) chr4: 17,807,915-17,817,512 DCAF16, NCAPG
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