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Items: 1 to 20 of 181

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3149722copy number variation1nstd151human GRCh37 (hg19) chr8: 144,375,140-144,403,561 , GRCh38 (hg38) chr8: 143,292,970-143,321,391 ZNF696, TOP1MT
    nsv3148477copy number variation1nstd151human GRCh37 (hg19) chr8: 144,295,140-144,408,519 , GRCh38 (hg38) chr8: 143,213,265-143,326,349 ZNF696, GPIHBP1, 4 more genes
    nsv3146324copy number variation1nstd151human GRCh37 (hg19) chr8: 144,332,011-144,417,036 , GRCh38 (hg38) chr8: 143,249,841-143,334,866 ZNF696, MINCR, 3 more genes
    nsv3141452copy number variation1nstd151human GRCh37 (hg19) chr8: 144,375,140-144,417,036 , GRCh38 (hg38) chr8: 143,292,970-143,334,866 ZNF696, TOP1MT
    nsv3110082copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr8: 86,841,154-146,295,771 , GRCh38 (hg38) chr8: 85,828,925-145,070,385 , NCBI36 (hg18) chr8: 86,910,442-146,266,575 ZNF696, ANGPT1, 818 more genes
    nsv3110077copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr8: 131,751,745-146,250,824 , GRCh37 (hg19) chr8: 131,682,563-146,280,020 , GRCh38 (hg38) chr8: 130,670,317-145,054,634 ZNF696, LOC105375773, 248 more genes
    nsv3109761copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr8: 12,490,999-146,295,771 , GRCh38 (hg38) chr8: 12,633,490-145,070,385 , NCBI36 (hg18) chr8: 12,535,370-146,266,575 ZNF696, MIR3150BHG, 1863 more genes
    esv4010889copy number variation1estd233human GRCh37 (hg19) chr8: 142,280,000-145,538,000 , GRCh38 (hg38) chr8: 141,269,901-144,314,337 ZNF696, ADGRB1, 114 more genes
    nsv3089551mobile element insertion1nstd144human GRCh37 (hg19) chr8: 144,370,623-144,370,623 , GRCh38 (hg38) chr8: 143,288,453-143,288,453 ZNF696
    nsv2787125copy number variation1nstd132human NCBI36 (hg18) chr8: 144,436,949-144,803,169 , GRCh37 (hg19) chr8: 144,365,574-144,732,026 , GRCh38 (hg38) chr8: 143,283,404-143,649,856 ZNF696, GSDMD, 19 more genes
    nsv2786931copy number variation1nstd132human NCBI36 (hg18) chr8: 144,355,026-144,785,990 , GRCh37 (hg19) chr8: 144,283,651-144,714,847 , GRCh38 (hg38) chr8: 143,202,190-143,632,677 ZNF696, ZC3H3, 22 more genes
    nsv2782180copy number variation1nstd132human NCBI36 (hg18) chr8: 144,436,949-144,796,206 , GRCh37 (hg19) chr8: 144,365,574-144,725,063 , GRCh38 (hg38) chr8: 143,283,404-143,642,893 ZNF696, EEF1D, 19 more genes
    nsv2777932copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr8: 98,432,250-146,222,672 , GRCh38 (hg38) chr8: 97,420,022-144,997,286 , NCBI36 (hg18) chr8: 98,501,426-146,193,476 ZNF696, ANXA13, 670 more genes
    nsv2776525copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr8: 127,707,788-144,459,935 , GRCh37 (hg19) chr8: 127,638,606-144,388,560 , GRCh38 (hg38) chr8: 126,626,361-143,306,390 ZNF696, ADCY8, 184 more genes
    nsv2776038copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr8: 3,938-146,274,826 , GRCh37 (hg19) chr8: 13,938-146,304,022 , GRCh38 (hg38) chr8: 63,938-145,078,636 ZNF696, NATP, 2163 more genes
    nsv2774782copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr8: 158,991-146,280,828 , GRCh38 (hg38) chr8: 208,991-145,055,442 , NCBI36 (hg18) chr8: 148,991-146,251,632 ZNF696, ACTBP6, 2159 more genes
    nsv2774617copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr8: 114,853,126-146,295,771 , GRCh38 (hg38) chr8: 113,840,897-145,070,385 , NCBI36 (hg18) chr8: 114,922,302-146,266,575 ZNF696, JRK, 451 more genes
    nsv2773496copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr8: 134,825,277-146,280,828 , GRCh38 (hg38) chr8: 133,813,034-145,055,442 , NCBI36 (hg18) chr8: 134,894,459-146,251,632 ZNF696, EEF1D, 210 more genes
    nsv2771836copy number variation1nstd37humanLikely pathogenic GRCh37 (hg19) chr8: 136,378,789-146,295,771 , GRCh38 (hg38) chr8: 135,366,546-145,070,385 , NCBI36 (hg18) chr8: 136,447,971-146,266,575 ZNF696, TIGD5, 199 more genes
    nsv2771806copy number variation5nstd37humanPathogenic GRCh37 (hg19) chr8: 158,049-146,295,771 , GRCh38 (hg38) chr8: 208,049-145,070,385 , NCBI36 (hg18) chr8: 148,049-146,266,575 ZNF696, FAM90A17P, 2160 more genes
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