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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv2777712copy number variation1nstd37humanBenign NCBI36 (hg18) chr1: 146,290,836-148,084,392 , GRCh37 (hg19) chr1: 147,824,212-149,817,768 , GRCh38 (hg38) chr7: 61,006,478-62,410,831 TRN-GTT7-1, TRN-GTT8-1, 33 more genes
    nsv2772868copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr1: 849,467-249,224,684 , GRCh38 (hg38) chr1: 914,087-248,930,485 , NCBI36 (hg18) chr1: 839,330-247,191,307 AKT3, MIR942, 2723 more genes
    nsv2772605copy number variation1nstd37humanBenign NCBI36 (hg18) chr1: 147,148,399-148,084,392 , GRCh37.p13 chr1|NW_003871055.3: 237,549-3,217,380 , GRCh37 (hg19) chr1: 148,881,775-149,817,768 , GRCh38 (hg38) chr7: 61,006,478-62,410,831 TRN-GTT8-1, TRV-CAC8-1, 18 more genes
    nsv2772284copy number variation1nstd37humanBenign NCBI36 (hg18) chr1: 147,203,306-148,084,392 , GRCh37 (hg19) chr1: 148,936,682-149,817,768 , GRCh37.p13 chr1|NW_003871055.3: 221,366-3,215,745 , GRCh38 (hg38) chr7: 61,006,478-62,410,831 TRN-GTT8-1, TRV-CAC8-1, 18 more genes
    nsv2771788copy number variation1nstd37humanBenign NCBI36 (hg18) chr1: 146,327,235-148,084,392 , GRCh37 (hg19) chr1: 147,860,611-149,817,768 , GRCh38 (hg38) chr7: 61,006,478-62,410,831 TRN-GTT7-1, TRN-GTT8-1, 33 more genes
    nsv2770337copy number variation1nstd37humanBenign NCBI36 (hg18) chr1: 147,134,258-148,084,392 , GRCh37 (hg19) chr1: 148,867,634-149,817,768 , GRCh37.p13 chr1|NW_003871055.3: 253,712-3,217,380 , GRCh38 (hg38) chr7: 61,006,478-62,410,831 TRN-GTT8-1, TRV-CAC8-1, 18 more genes
    nsv2770146copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr1: 144,764,751-247,199,719 , GRCh37 (hg19) chr1: 146,053,394-249,233,096 , GRCh38 (hg38) chr1: 120,836,007-248,938,897 AKT3, MIR190B, 1326 more genes
    nsv2768411copy number variation3nstd37humanBenign NCBI36 (hg18) chr1: 147,083,653-148,084,392 , GRCh37 (hg19) chr1: 148,817,029-149,817,768 , GRCh37.p13 chr1|NW_003871055.3: 234,081-3,217,380 , GRCh38 (hg38) chr7: 61,006,478-62,410,831 TRN-GTT8-1, TRV-CAC8-1, 19 more genes
    nsv2768399copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr1: 144,475,856-247,199,719 , GRCh37 (hg19) chr1: 145,764,499-249,233,096 , GRCh38 (hg38) chr1: 120,836,007-248,938,897 AKT3, MIR190B, 1329 more genes
    nsv2768300copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr1: 143,753,740-151,399,970 , GRCh38 (hg38) chr1: 120,155,785-149,362,826 , GRCh38 (hg38) chr7: 58,093,723-62,422,888 , NCBI36 (hg18) chr1: 142,545,263-149,666,594 TRNAN-GUU, NBPF10, 186 more genes
    nsv1398121copy number variation1nstd102humanUncertain significance NCBI36 (hg18) chr1: 148,050,312-148,315,653 , GRCh37 (hg19) chr1: 149,783,688-150,049,029 , GRCh38 (hg38) chr1: 149,812,133-150,076,951 SF3B4, MTMR11, 15 more genes
    nsv1305941copy number variation1nstd122human NCBI36 (hg18) chr1: 148,065,230-148,085,090 , GRCh37 (hg19) chr1: 149,798,606-149,818,466 , GRCh38 (hg38) chr1: 149,827,053-149,846,899 HIST2H3C, HIST2H2AA3, 1 more genes
    nsv1192825copy number variation1nstd113human NCBI36 (hg18) chr1: 144,124,544-152,437,883 , GRCh37 (hg19) chr1: 145,413,187-154,171,259 , GRCh38 (hg38) chr1: 120,836,007-149,583,533 MIR190B, C1orf68, 280 more genes
    nsv1148209copy number variation1nstd107human GRCh37 (hg19) chr1: 144,023,427-206,486,111 , GRCh38 (hg38) chr1: 120,323,082-206,312,767 MIR190B, MIR921, 931 more genes
    nsv1146931inversion1nstd107human GRCh37 (hg19) chr1: 6,858,651-214,875,307 , GRCh38 (hg38) chr1: 6,798,591-214,701,964 MIR942, MIR190B, 2283 more genes
    nsv1137291copy number variation1nstd106human GRCh37 (hg19) chr1: 144,023,484-206,486,113 , GRCh38 (hg38) chr1: 120,323,082-206,312,769 MIR190B, MIR921, 931 more genes
    nsv1132997inversion1nstd106human GRCh37 (hg19) chr1: 16,843,414-234,953,211 , GRCh38 (hg38) chr1: 16,516,919-234,817,464 MIR942, MIR190B, 2310 more genes
    esv3815443copy number variation1estd192human GRCh37 (hg19) chr1: 14,660,218-180,369,490 , GRCh38 (hg38) chr1: 14,333,723-180,400,355 MIR942, MIR190B, 1859 more genes
    esv3802655tandem duplication1estd192human GRCh37 (hg19) chr1: 80,813,950-184,281,458 , GRCh38 (hg38) chr1: 80,348,265-184,312,324 MIR942, MIR190B, 1093 more genes
    esv3812944copy number variation1estd192human GRCh37 (hg19) chr1: 22,511,560-229,652,792 , GRCh38 (hg38) chr1: 22,185,067-229,517,045 MIR942, MIR190B, 2167 more genes
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