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Items: 1 to 20 of 1817

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3146277copy number variation1nstd151human GRCh37 (hg19) chr11: 130,748,314-132,527,219 , GRCh38 (hg38) chr11: 130,878,419-132,657,324 NTM, SNX19, 13 more genes
    nsv3144938copy number variation1nstd151human GRCh37 (hg19) chr11: 128,332,253-134,226,292 , GRCh38 (hg38) chr11: 128,462,358-134,356,398 NTM, ETS1, 83 more genes
    nsv3144618copy number variation1nstd151human GRCh37 (hg19) chr11: 130,748,314-131,240,788 , GRCh38 (hg38) chr11: 130,878,419-131,370,893 NTM, SNX19, 6 more genes
    nsv3142831copy number variation1nstd151human GRCh37 (hg19) chr11: 132,180,003-132,205,045 , GRCh38 (hg38) chr11: 132,310,109-132,335,151 NTM
    nsv3140491copy number variation2nstd151human GRCh37 (hg19) chr11: 132,177,580-132,205,045 , GRCh38 (hg38) chr11: 132,307,686-132,335,151 NTM
    nsv3115625copy number variation1nstd145human GRCh37 (hg19) chr11: 131,744,641-131,751,629 , GRCh38 (hg38) chr11: 131,874,747-131,881,735 NTM, LOC107984413
    nsv3115409copy number variation2nstd145human GRCh37 (hg19) chr11: 131,779,002-131,780,186 , GRCh38 (hg38) chr11: 131,909,108-131,910,292 NTM, LOC107984413
    nsv3115007copy number variation3nstd145human GRCh37 (hg19) chr11: 131,719,880-131,724,306 , GRCh38 (hg38) chr11: 131,849,986-131,854,412 NTM
    nsv3114523copy number variation1nstd145human GRCh37 (hg19) chr11: 131,719,902-131,724,306 , GRCh38 (hg38) chr11: 131,850,008-131,854,412 NTM
    nsv3113083copy number variation2nstd145human GRCh37 (hg19) chr11: 131,779,020-131,780,859 , GRCh38 (hg38) chr11: 131,909,126-131,910,965 NTM, LOC107984413
    nsv3112889copy number variation1nstd145human GRCh37 (hg19) chr11: 131,777,910-131,784,059 , GRCh38 (hg38) chr11: 131,908,016-131,914,165 NTM, LOC107984413
    nsv3110718copy number variation1nstd145human GRCh37 (hg19) chr11: 131,779,002-131,780,859 , GRCh38 (hg38) chr11: 131,909,108-131,910,965 NTM, LOC107984413
    nsv3110003copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chr11: 131,564,105-131,933,922 , GRCh37 (hg19) chr11: 132,058,895-132,428,712 , GRCh38 (hg38) chr11: 132,189,001-132,558,817 NTM, OPCML, 1 more genes
    nsv3110002copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr11: 122,884,694-134,938,470 , GRCh38 (hg38) chr11: 123,013,986-135,068,576 , NCBI36 (hg18) chr11: 122,389,904-134,443,680 NTM, OR8G2P, 253 more genes
    nsv3109670copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr11: 123,365,495-134,373,617 , GRCh37 (hg19) chr11: 123,860,285-134,868,407 , GRCh38 (hg38) chr11: 123,989,578-134,998,513 NTM, TMEM218, 219 more genes
    nsv3073596copy number variation1nstd144human GRCh37 (hg19) chr11: 132,083,626-132,083,927 , GRCh38 (hg38) chr11: 132,213,732-132,214,033 NTM
    nsv3073595mobile element insertion1nstd144human GRCh37 (hg19) chr11: 131,615,848-131,615,848 , GRCh38 (hg38) chr11: 131,745,954-131,745,954 NTM
    nsv3073594mobile element insertion1nstd144human GRCh37 (hg19) chr11: 131,527,630-131,527,630 , GRCh38 (hg38) chr11: 131,657,736-131,657,736 NTM
    nsv3073593mobile element insertion1nstd144human GRCh37 (hg19) chr11: 131,361,338-131,361,338 , GRCh38 (hg38) chr11: 131,491,444-131,491,444 NTM
    nsv3073442copy number variation1nstd144human GRCh37 (hg19) chr11: 131,502,573-131,502,863 , GRCh38 (hg38) chr11: 131,632,679-131,632,969 NTM
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