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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978979insertion1nstd209human GRCh38 chr20: 34,950,020-34,950,020 , GRCh37.p13 chr20: 33,537,823-33,537,823 GSS
    nsv5701179mobile element insertion1nstd211human GRCh38 chr20: 34,951,625-34,951,625 , GRCh37.p13 chr20: 33,539,428-33,539,428 GSS
    nsv5416545mobile element insertion1nstd206human GRCh38 chr20: 34,951,625-34,951,676 , GRCh37.p13 chr20: 33,539,428-33,539,479 GSS
    nsv5366092translocation1nstd200human GRCh38 chr20: 34,953,738-34,953,738 , GRCh38 chr20: 34,952,658-34,952,658 , GRCh37.p13 chr20: 33,541,541-33,541,541 , GRCh37.p13 chr20: 33,540,461-33,540,461 GSS
    nsv5333459translocation1nstd200human GRCh37 chr20: 33,529,096-33,529,096 , GRCh37 chr20: 33,531,836-33,531,836 , GRCh38.p12 chr20: 34,941,293-34,941,293 , GRCh38.p12 chr20: 34,944,033-34,944,033 GSS
    nsv5171065mobile element insertion1nstd203human GRCh38 chr20: 34,951,611-34,951,625 , GRCh37.p13 chr20: 33,539,414-33,539,428 GSS
    nsv5170184mobile element insertion1nstd203human GRCh38 chr20: 34,950,911-34,950,925 , GRCh37.p13 chr20: 33,538,714-33,538,728 GSS
    nsv5022343copy number variation1nstd200human GRCh38 chr20: 32,602,560-45,347,064 , GRCh37.p13 chr20: 31,190,362-43,975,704 , SNHG11, 286 more genes
    nsv5022342copy number variation1nstd200human GRCh38 chr20: 32,576,247-46,538,786 , GRCh37.p13 chr20: 31,164,049-45,167,425 , NECAB3, 350 more genes
    nsv5022326copy number variation1nstd200human GRCh38 chr20: 32,216,214-44,981,731 , GRCh37.p13 chr20: 30,804,017-43,610,372 , HNF4A, 279 more genes
    nsv4868682copy number variation1nstd200human GRCh37 chr20: 33,540,453-33,541,584 , GRCh38.p12 chr20: 34,952,650-34,953,781 GSS
    nsv4868593copy number variation1nstd200human GRCh37 chr20: 31,164,049-45,167,425 , GRCh38.p12 chr20: 32,576,247-46,538,786 , MMP24-AS1-EDEM2, 350 more genes
    nsv4868578copy number variation1nstd200human GRCh37 chr20: 30,804,017-43,610,372 , GRCh38.p12 chr20: 32,216,214-44,981,731 , SNORA71C, 279 more genes
    nsv4515961mobile element insertion1nstd166human GRCh37.p13 chr20: 33,538,714-33,538,714 , GRCh38.p12 chr20: 34,950,911-34,950,911 GSS
    nsv4511016mobile element insertion1nstd166human GRCh37.p13 chr20: 33,539,414-33,539,414 , GRCh38.p12 chr20: 34,951,611-34,951,611 GSS
    nsv4499336mobile element insertion1nstd166human GRCh37.p13 chr20: 33,525,306-33,525,306 , GRCh38.p12 chr20: 34,937,503-34,937,503 GSS
    nsv4457806copy number variation1nstd102humanPathogenic GRCh37 chr20: 29,833,608-35,087,952 , GRCh38.p12 chr20: 31,245,805-36,459,549 EFCAB8, C20orf203, 162 more genes
    nsv3920503copy number variation1nstd102humanPathogenic GRCh38 chr20: 32,062,768-35,906,606 , NCBI36 chr20: 30,114,232-33,957,942 , GRCh37 chr20: 30,650,571-34,494,528 UQCC1, MIR1289-1, 111 more genes
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 MIR3646, NPEPL1, 1310 more genes
    nsv3918053copy number variation1nstd102humanPathogenic NCBI36 chr20: 25,703,100-38,491,480 , GRCh37.p13 chr20: 25,755,100-39,058,066 , GRCh38.p12 chr20: 25,774,464-40,429,426 MYH7B, PPP1R16B, 300 more genes
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