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Items: 1 to 20 of 817

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv2788076copy number variation1nstd132human NCBI36 (hg18) chr17: 76,893,405-77,703,095 , GRCh37 (hg19) chr17: 79,278,810-80,109,806 , GRCh38 (hg38) chr17: 81,305,010-82,151,930 MIR3186, MIR4740, 43 more genes
    nsv2787364copy number variation1nstd132human NCBI36 (hg18) chr17: 77,288,155-77,575,566 , GRCh37 (hg19) chr17: 79,677,750-79,982,277 , GRCh38 (hg38) chr17: 81,710,720-82,024,401 ALYREF, PPP1R27, 17 more genes
    nsv2787221copy number variation1nstd132human NCBI36 (hg18) chr17: 77,222,566-77,638,015 , GRCh37 (hg19) chr17: 79,612,161-80,044,726 , GRCh38 (hg38) chr17: 81,645,135-82,086,850 ALYREF, MIR6786, 31 more genes
    nsv2787148copy number variation1nstd132human NCBI36 (hg18) chr17: 77,202,218-77,703,095 , GRCh37 (hg19) chr17: 79,591,813-80,109,806 , GRCh38 (hg38) chr17: 81,624,787-82,151,930 ALYREF, MIR6786, 34 more genes
    nsv2786920copy number variation2nstd132human NCBI36 (hg18) chr17: 77,288,155-77,638,015 , GRCh37 (hg19) chr17: 79,677,750-80,044,726 , GRCh38 (hg38) chr17: 81,710,720-82,086,850 ALYREF, PPP1R27, 23 more genes
    nsv2785925copy number variation1nstd132human NCBI36 (hg18) chr17: 76,893,405-77,638,015 , GRCh37 (hg19) chr17: 79,278,810-80,044,726 , GRCh38 (hg38) chr17: 81,305,010-82,086,850 MIR3186, MIR4740, 41 more genes
    nsv2785885copy number variation2nstd132human NCBI36 (hg18) chr17: 77,298,298-77,638,015 , GRCh37 (hg19) chr17: 79,687,893-80,044,726 , GRCh38 (hg38) chr17: 81,720,863-82,086,850 ALYREF, PPP1R27, 23 more genes
    nsv2784450copy number variation2nstd132human NCBI36 (hg18) chr17: 77,222,566-77,703,095 , GRCh37 (hg19) chr17: 79,612,161-80,109,806 , GRCh38 (hg38) chr17: 81,645,135-82,151,930 ALYREF, MIR6786, 33 more genes
    nsv2784413copy number variation1nstd132human NCBI36 (hg18) chr17: 77,379,857-77,638,015 , GRCh37 (hg19) chr17: 79,786,568-80,044,726 , GRCh38 (hg38) chr17: 81,828,692-82,086,850 ALYREF, PPP1R27, 21 more genes
    nsv2779082copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr17: 42,580,684-81,085,615 , GRCh38 (hg38) chr17: 44,503,316-83,137,846 , NCBI36 (hg18) chr17: 39,936,210-78,641,478 SNORA38B, MAPT-AS1, 613 more genes
    nsv2779064copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr17: 67,002,415-81,041,938 , GRCh38 (hg38) chr17: 69,006,274-83,084,062 , NCBI36 (hg18) chr17: 64,514,010-78,635,227 SMIM6, TNRC6C-AS1, 276 more genes
    nsv2778886copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr22: 49,305,443-51,197,838 , GRCh38 (hg38) chr22: 48,909,631-50,759,410 , NCBI36 (hg18) chr22: 47,691,447-49,544,704 CHKB-AS1, MIR3667, 38 more genes
    nsv2778854copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr17: 73,951,701-81,041,938 , GRCh38 (hg38) chr17: 75,955,620-83,084,062 , NCBI36 (hg18) chr17: 71,463,296-78,635,227 TNRC6C-AS1, TEN1, 172 more genes
    nsv2778637copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr22: 48,556,939-51,197,838 , GRCh38 (hg38) chr22: 48,161,122-50,759,410 , NCBI36 (hg18) chr22: 46,935,603-49,544,704 LINC01310, CHKB-AS1, 42 more genes
    nsv2778625copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr22: 49,628,164-51,197,838 , GRCh38 (hg38) chr22: 49,232,238-50,759,410 , NCBI36 (hg18) chr22: 48,014,168-49,544,704 CHKB-AS1, MIR3667, 38 more genes
    nsv2778620copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr1: 103,429,843-112,252,782 , GRCh37 (hg19) chr1: 103,657,255-112,451,259 , GRCh38 (hg38) chr1: 103,191,699-111,908,637 LINC01160, FAM212B-AS1, 94 more genes
    nsv2778209copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr1: 93,837,992-121,343,783 , GRCh38 (hg38) chr1: 93,372,435-144,935,242 , NCBI36 (hg18) chr1: 93,610,580-121,045,306 MIR942, MIR760, 278 more genes
    nsv2777911copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr22: 47,274,872-49,591,432 , GRCh37 (hg19) chr22: 48,896,208-51,203,353 , GRCh38 (hg38) chr22: 48,500,396-50,806,138 LINC01310, CHKB-AS1, 42 more genes
    nsv2777619copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr22: 47,187,586-51,237,463 , GRCh38 (hg38) chr22: 46,791,689-50,799,035 , NCBI36 (hg18) chr22: 45,566,250-49,584,329 LPEQ6126, LINC01310, 48 more genes
    nsv2777516copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr22: 47,247,169-51,176,099 , GRCh38 (hg38) chr22: 46,851,273-50,737,671 , NCBI36 (hg18) chr22: 45,625,833-49,522,965 LPEQ6126, LINC01310, 46 more genes
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