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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1195931copy number variation1nstd113human NCBI36 (hg18) chr17: 6,716,420-8,264,897 , GRCh37 (hg19) chr17: 6,775,696-8,324,172 , GRCh38 (hg38) chr17: 6,872,377-8,420,854 TRS-CGA1-1, TRW-CCA3-1, 114 more genes
    nsv1194385copy number variation1nstd113human NCBI36 (hg18) chr17: 52,934-8,545,428 , GRCh37 (hg19) chr17: 52,934-8,604,703 , GRCh38 (hg38) chr17: 203,143-8,701,385 C17orf107, TRS-CGA1-1, 258 more genes
    nsv1194214copy number variation1nstd113human NCBI36 (hg18) chr17: 53,448-20,145,464 , GRCh37 (hg19) chr17: 396,627-20,204,872 , GRCh38 (hg38) chr17: 203,657-20,301,559 MIR744, MYHAS, 405 more genes
    nsv1190880copy number variation1nstd113human NCBI36 (hg18) chr17: 6,922,591-7,187,372 , GRCh37 (hg19) chr17: 6,981,867-7,246,648 , GRCh38 (hg38) chr17: 7,078,548-7,343,329 CLEC10A, GABARAP, 16 more genes
    nsv1141883inversion1nstd106human GRCh37 (hg19) chr17: 5,045,567-58,288,633 , GRCh38 (hg38) chr17: 5,142,272-60,211,272 MIR744, MIR365B, 961 more genes
    esv3639865copy number variation2estd214human GRCh37 (hg19) chr17: 7,196,105-7,225,856 , GRCh38 (hg38) chr17: 7,292,786-7,322,537 EIF5A, GPS2, 2 more genes
    nsv1067273copy number variation1nstd100human GRCh37 (hg19) chr17: 6,981,867-7,246,648 , GRCh38 (hg38) chr17: 7,078,548-7,343,329 , NCBI36 (hg18) chr17: 6,922,591-7,187,372 CLEC10A, GABARAP, 16 more genes
    nsv1062350copy number variation1nstd100human GRCh37 (hg19) chr17: 396,627-20,204,872 , GRCh38 (hg38) chr17: 203,657-20,301,559 , NCBI36 (hg18) chr17: 53,448-20,145,464 MIR744, MYHAS, 402 more genes
    nsv1060463copy number variation1nstd100human GRCh37 (hg19) chr17: 52,934-8,604,703 , GRCh38 (hg38) chr17: 203,143-8,701,385 , NCBI36 (hg18) chr17: 52,934-8,545,428 C17orf107, TRS-CGA1-1, 257 more genes
    nsv1058431copy number variation1nstd100human GRCh37 (hg19) chr17: 7,113,526-7,407,317 , GRCh38 (hg38) chr17: 7,210,207-7,503,998 , NCBI36 (hg18) chr17: 7,054,250-7,348,041 TMEM256-PLSCR3, GABARAP, 28 more genes
    nsv1058181copy number variation1nstd100human GRCh37 (hg19) chr17: 6,775,696-8,324,172 , GRCh38 (hg38) chr17: 6,872,377-8,420,854 , NCBI36 (hg18) chr17: 6,716,420-8,264,897 TRS-CGA1-1, TRW-CCA3-1, 114 more genes
    nsv1057252copy number variation1nstd100human GRCh37 (hg19) chr17: 6,963,754-7,688,015 , GRCh38 (hg38) chr17: 7,060,435-7,784,697 , NCBI36 (hg18) chr17: 6,904,478-7,628,740 TMEM256-PLSCR3, SENP3-EIF4A1, 51 more genes
    nsv1056674copy number variation1nstd100human GRCh37 (hg19) chr17: 6,232,306-8,744,804 , GRCh38 (hg38) chr17: 6,328,986-8,841,487 , NCBI36 (hg18) chr17: 6,173,030-8,685,529 TRS-CGA1-1, TRW-CCA3-1, 133 more genes
    esv3567885copy number variation1estd211human GRCh37 (hg19) chr17: 7,214,801-7,902,885 , GRCh38 (hg38) chr17: 7,311,482-7,999,567 TMEM256-PLSCR3, SENP3-EIF4A1, 46 more genes
    esv3567883copy number variation1estd211human GRCh37 (hg19) chr17: 7,008,107-7,264,335 , GRCh38 (hg38) chr17: 7,104,788-7,361,016 GABARAP, CLDN7, 17 more genes
    nsv996083copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr17: 525-14,667,519 , GRCh38 (hg38) chr17: 150,732-14,764,202 , NCBI36 (hg18) chr17: 525-14,608,244 MIR744, MYHAS, 302 more genes
    nsv984832copy number variation2nstd11humannot provided NCBI36 (hg18) chr17: 526-78,643,088 , GRCh37 (hg19) chr17: 45,835-81,048,189 , GRCh38 (hg38) chr17: 155,903-83,091,923 SNORA38B, MIR744, 1434 more genes
    nsv984824copy number variation1nstd92human GRCh37 (hg19) chr17: 88,964-21,461,735 , GRCh38 (hg38) chr17: 239,173-21,558,472 MIR744, MYHAS, 417 more genes
    nsv984771copy number variation1nstd92human GRCh37 (hg19) chr17: 2,220-19,238,441 , GRCh38 (hg38) chr17: 152,427-19,335,128 MIR744, MYHAS, 390 more genes
    nsv959743copy number variation1nstd86human GRCh37 (hg19) chr17: 7,133,602-7,259,800 , GRCh38 (hg38) chr17: 7,230,283-7,356,481 GABARAP, CLDN7, 12 more genes
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