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Results: 1 to 20 of 303

  • The following terms were not found in dbVar: Leafy, Dragons.
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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1067759copy number variation1nstd101humanPathogenic NCBI36 (hg18) chr22: 17,299,942-19,038,934 , GRCh37 (hg19) chr22: 18,919,942-20,708,934 , GRCh38 (hg38) chr22: 18,339,130-20,354,644 MIR1286, MIR1306, 47 more genes
    nsv1067758copy number variation18nstd101humanPathogenic NCBI36 (hg18) chr22: 17,299,942-19,835,417 , GRCh37 (hg19) chr22: 18,919,942-21,505,417 , GRCh38 (hg38) chr22: 18,339,130-21,151,128 MIR1286, MIR1306, 64 more genes
    nsv1067757copy number variation3nstd101humanPathogenic NCBI36 (hg18) chr22: 17,299,942-20,139,009 , GRCh37 (hg19) chr22: 18,919,942-21,809,009 , GRCh38 (hg38) chr22: 18,339,130-21,454,720 MIR1286, MIR1306, 67 more genes
    nsv1067755copy number variation1nstd101humanPathogenic NCBI36 (hg18) chr22: 17,086,001-18,989,606 , GRCh37 (hg19) chr22: 18,706,001-20,659,606 , GRCh38 (hg38) chr22: 18,339,130-20,343,532 MIR1286, MIR1306, 46 more genes
    nsv1067754copy number variation3nstd101humanPathogenic NCBI36 (hg18) chr22: 17,086,001-19,770,514 , GRCh37 (hg19) chr22: 18,706,001-21,440,514 , GRCh38 (hg38) chr22: 18,339,130-21,086,225 MIR1286, MIR1306, 64 more genes
    nsv1067753copy number variation4nstd101humanPathogenic NCBI36 (hg18) chr22: 17,086,001-19,835,417 , GRCh37 (hg19) chr22: 18,706,001-21,505,417 , GRCh38 (hg38) chr22: 18,339,130-21,151,128 MIR1286, MIR1306, 64 more genes
    nsv1067750copy number variation2nstd101humanPathogenic NCBI36 (hg18) chr22: 17,041,724-19,835,417 , GRCh37 (hg19) chr22: 18,661,724-21,505,417 , GRCh38 (hg38) chr22: 18,178,957-21,151,128 MIR1286, MIR1306, 64 more genes
    nsv1067749copy number variation3nstd101humanPathogenic NCBI36 (hg18) chr22: 17,041,724-19,770,514 , GRCh37 (hg19) chr22: 18,661,724-21,440,514 , GRCh38 (hg38) chr22: 18,178,957-21,086,225 MIR1286, MIR1306, 64 more genes
    nsv1067748copy number variation1nstd101humanPathogenic NCBI36 (hg18) chr22: 17,008,019-19,835,417 , GRCh37 (hg19) chr22: 18,628,019-21,505,417 , GRCh38 (hg38) chr22: 18,145,252-21,151,128 MIR1286, MIR1306, 65 more genes
    nsv1067671copy number variation2nstd101humanPathogenic NCBI36 (hg18) chr22: 17,086,001-19,355,713 , GRCh37 (hg19) chr22: 18,706,001-21,025,713 , GRCh38 (hg38) chr22: 18,339,130-20,671,425 MIR1286, MIR1306, 52 more genes
    nsv1067636copy number variation1nstd101humanPathogenic NCBI36 (hg18) chr22: 17,299,942-18,691,763 , GRCh37 (hg19) chr22: 18,919,942-20,311,763 , GRCh38 (hg38) chr22: 18,932,429-20,324,240 MIR1286, MIR1306, 41 more genes
    nsv1067635copy number variation8nstd101humanPathogenic NCBI36 (hg18) chr22: 17,299,942-19,770,514 , GRCh37 (hg19) chr22: 18,919,942-21,440,514 , GRCh38 (hg38) chr22: 18,339,130-21,086,225 MIR1286, MIR1306, 64 more genes
    nsv1067576copy number variation1nstd101humanPathogenic NCBI36 (hg18) chr22: 17,299,942-18,989,606 , GRCh37 (hg19) chr22: 18,919,942-20,659,606 , GRCh38 (hg38) chr22: 18,339,130-20,343,532 MIR1286, MIR1306, 46 more genes
    nsv1067571copy number variation11nstd101humanPathogenic NCBI36 (hg18) chr22: 17,299,942-19,891,514 , GRCh37 (hg19) chr22: 18,919,942-21,561,514 , GRCh38 (hg38) chr22: 18,339,130-21,207,225 MIR1286, MIR1306, 64 more genes
    nsv1067567copy number variation2nstd101humanPathogenic NCBI36 (hg18) chr22: 17,041,724-19,891,514 , GRCh37 (hg19) chr22: 18,661,724-21,561,514 , GRCh38 (hg38) chr22: 18,178,957-21,207,225 MIR1286, MIR1306, 64 more genes
    esv3575418copy number variation1estd212human GRCh38 (hg38) chr22: 18,161,776-19,963,846 , GRCh37 (hg19) chr22: 18,644,543-19,951,369 SEPT5-GP1BB, MIR4761, 33 more genes
    esv3575429copy number variation1estd212human GRCh38 (hg38) chr22: 18,339,130-21,444,618 , GRCh37 (hg19) chr22: 19,954,391-21,798,907 MIR1286, MIR1306, 67 more genes
    esv3575420copy number variation1estd212human GRCh37 (hg19) chr22: 18,648,867-21,465,659 , GRCh38 (hg38) chr22: 18,166,100-21,111,370 MIR1286, MIR1306, 65 more genes
    nsv1067479copy number variation7nstd100human NCBI36 (hg18) chr22: 17,299,741-19,770,654 , GRCh37 (hg19) chr22: 18,919,741-21,440,654 , GRCh38 (hg38) chr22: 18,339,130-21,086,365 MIR1286, MIR1306, 64 more genes
    nsv1067107copy number variation1nstd100human NCBI36 (hg18) chr22: 17,256,416-19,941,337 , GRCh37 (hg19) chr22: 18,876,416-21,611,337 , GRCh38 (hg38) chr22: 18,339,130-21,257,048 MIR1286, MIR1306, 65 more genes

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