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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3135569copy number variation1nstd151human GRCh37 (hg19) chr6: 139,094,809-139,101,127 , GRCh38 (hg38) chr6: 138,773,672-138,779,990 GVQW2, CCDC28A
    nsv3133716copy number variation1nstd151human GRCh37 (hg19) chr6: 139,094,809-139,106,523 , GRCh38 (hg38) chr6: 138,773,672-138,785,386 CCDC28A, GVQW2
    nsv3131470copy number variation1nstd151human GRCh37 (hg19) chr6: 139,094,809-139,135,745 , GRCh38 (hg38) chr6: 138,773,672-138,814,608 CCDC28A, ECT2L, 1 more genes
    nsv3109842copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr6: 124,322,082-156,156,864 , GRCh37 (hg19) chr6: 124,280,383-156,115,172 , GRCh38 (hg38) chr6: 123,959,238-155,794,038 EPM2A, LOC100507557, 436 more genes
    esv4010717copy number variation1estd233human GRCh37 (hg19) chr6: 136,235,000-167,697,000 , GRCh38 (hg38) chr6: 135,913,862-167,283,512 ACAT2, CCR6, 436 more genes
    nsv2779086copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr6: 156,975-170,919,482 , GRCh38 (hg38) chr6: 156,975-170,610,394 , NCBI36 (hg18) chr6: 101,975-170,761,407 LOC107986551, HMGB1P13, 3007 more genes
    nsv2776705copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr6: 136,359,437-146,708,473 , GRCh37 (hg19) chr6: 136,317,744-146,666,780 , GRCh38 (hg38) chr6: 135,996,606-146,345,644 IFNGR1, PEX7, 132 more genes
    nsv2775088copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr6: 121,373,749-146,289,101 , GRCh37 (hg19) chr6: 121,332,050-146,247,408 , GRCh38 (hg38) chr6: 121,010,904-145,926,272 ARG1, EYA4, 330 more genes
    nsv2770228copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr6: 133,077,239-143,761,582 , GRCh38 (hg38) chr6: 132,756,100-143,440,445 , NCBI36 (hg18) chr6: 133,118,932-143,803,275 HEBP2, PDE7B, 153 more genes
    nsv2469581short tandem repeat3nstd128human GRCh37 (hg19) chr6: 139,112,384-139,112,400 , GRCh38 (hg38) chr6: 138,791,247-138,791,263 CCDC28A
    nsv2469579short tandem repeat2nstd128human GRCh37 (hg19) chr6: 139,111,285-139,111,307 , GRCh38 (hg38) chr6: 138,790,148-138,790,170 CCDC28A
    nsv2469578short tandem repeat4nstd128human GRCh37 (hg19) chr6: 139,105,837-139,105,849 , GRCh38 (hg38) chr6: 138,784,700-138,784,712 CCDC28A
    nsv2469577short tandem repeat10nstd128human GRCh37 (hg19) chr6: 139,105,473-139,105,505 , GRCh38 (hg38) chr6: 138,784,336-138,784,368 CCDC28A
    nsv2469576short tandem repeat3nstd128human GRCh37 (hg19) chr6: 139,093,917-139,093,933 , GRCh38 (hg38) chr6: 138,772,780-138,772,796 CCDC28A, GVQW2
    nsv2469575short tandem repeat3nstd128human GRCh37 (hg19) chr6: 139,093,893-139,093,903 , GRCh38 (hg38) chr6: 138,772,756-138,772,766 GVQW2, CCDC28A
    nsv2443240short tandem repeat3nstd128human GRCh37 (hg19) chr6: 139,114,703-139,114,731 , GRCh38 (hg38) chr6: 138,793,566-138,793,594 CCDC28A
    nsv2443239short tandem repeat2nstd128human GRCh37 (hg19) chr6: 139,113,667-139,113,678 , GRCh38 (hg38) chr6: 138,792,530-138,792,541 CCDC28A
    nsv2443238short tandem repeat2nstd128human GRCh37 (hg19) chr6: 139,112,223-139,112,235 , GRCh38 (hg38) chr6: 138,791,086-138,791,098 CCDC28A
    nsv2443237short tandem repeat4nstd128human GRCh37 (hg19) chr6: 139,099,907-139,099,922 , GRCh38 (hg38) chr6: 138,778,770-138,778,785 CCDC28A
    nsv2443236short tandem repeat2nstd128human GRCh37 (hg19) chr6: 139,096,999-139,097,017 , GRCh38 (hg38) chr6: 138,775,862-138,775,880 CCDC28A
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