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Items: 15

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    Number of Variants: 15

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7136949copy number variation1nstd102humanPathogenic GRCh37 chr4: 103,790,345-103,813,965 , GRCh38.p12 chr4: 102,869,188-102,892,808 UBE2D3, CISD2, 1 more genes
    nsv7097220copy number variation1nstd102humanPathogenic GRCh37 chr4: 101,947,022-106,061,534 , GRCh38.p12 chr4: 101,025,865-105,140,377 UBE2D3, LOC100419096, 41 more genes
    nsv6311893copy number variation2nstd102humanPathogenic GRCh37 chr4: 101,947,022-104,640,832 , GRCh38.p12 chr4: 101,025,865-103,719,675 UBE2D3, LOC102723704, 32 more genes
    nsv7096485copy number variation1nstd102humanPathogenic GRCh37 chr4: 102,001,669-103,806,607 , GRCh38.p12 chr4: 101,080,512-102,885,450 UBE2D3, SLC9B1, 24 more genes
    nsv3873978copy number variation1nstd102humanPathogenic GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724 UBE2D3, LOC100422029, 2358 more genes
    nsv3876533copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611 UBE2D3, LOC100420289, 2347 more genes
    nsv3884499copy number variation1nstd102humanPathogenic GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286 UBE2D3, MTND4LP29, 2341 more genes
    nsv3880085copy number variation2nstd102humanPathogenic GRCh37 chr4: 68,346-190,957,473 , GRCh38.p12 chr4: 68,454-190,036,318 UBE2D3, LOC112268460, 2345 more genes
    nsv3883791copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-190,915,650 , GRCh38.p12 chr4: 49,556-189,994,495 UBE2D3, LOC105377343, 2341 more genes
    nsv3875534copy number variation1nstd102humanPathogenic GRCh37 chr4: 93,071,152-190,957,473 , GRCh38.p12 chr4: 92,150,001-190,036,318 UBE2D3, KLKB1, 1118 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 UBE2D3, SNHG27, 1091 more genes
    nsv3920388copy number variation1nstd102humanPathogenic GRCh37 chr4: 97,014,044-137,331,362 , NCBI36 chr4: 97,233,067-137,550,812 , GRCh38 chr4: 96,092,893-136,410,207 UBE2D3, MIR576, 447 more genes
    nsv6315383copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 102,851,823-104,641,864 , GRCh38.p12 chr4: 101,930,666-103,720,707 UBE2D3, CENPE, 26 more genes
    nsv6291428copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 95,490,755-109,977,216 , GRCh38.p12 chr4: 94,569,604-109,056,060 UBE2D3, ADH1A, 157 more genes
    nsv7098788copy number variation1nstd102humanUncertain significance GRCh37 chr4: 101,947,022-107,268,849 , GRCh38.p12 chr4: 101,025,865-106,347,692 UBE2D3, LOC107986297, 60 more genes
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