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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5620659insertion2nstd207human GRCh38 chr2: 3,531,062-3,531,062 , GRCh37.p8 chr: NaN-NaN , GRCh37.p13 chr: NaN-NaN RNASEH1
    nsv5620604insertion1nstd207human GRCh38 chr2: 3,530,890-3,530,890 , GRCh37.p8 chr: NaN-NaN , GRCh37.p13 chr: NaN-NaN RNASEH1
    nsv5615198insertion1nstd207human GRCh38 chr2: 3,531,071-3,531,071 , GRCh37.p8 chr: NaN-NaN , GRCh37.p13 chr: NaN-NaN RNASEH1
    nsv5609208insertion1nstd207human GRCh38 chr2: 3,530,653-3,530,653 , GRCh37.p8 chr: NaN-NaN , GRCh37.p13 chr: NaN-NaN RNASEH1
    nsv5606892insertion1nstd207human GRCh38 chr2: 3,530,769-3,530,769 , GRCh37.p8 chr: NaN-NaN , GRCh37.p13 chr: NaN-NaN RNASEH1
    nsv5559561sequence alteration1nstd206human GRCh38 chr2: 3,368,479-3,534,951 , GRCh37.p13 chr2: 3,372,250-3,582,541 EIPR1, TRAPPC12, 3 more genes
    nsv5449631copy number variation1nstd206human GRCh38 chr2: 3,530,612-3,530,956 , GRCh37.p13 chr: NaN-NaN RNASEH1
    nsv4904715copy number variation1nstd200human GRCh38 chr2: 3,499,847-3,538,421 , GRCh37.p13 chr2: 3,503,618-3,586,011 ADI1, RNASEH1
    nsv4904711copy number variation1nstd200human GRCh38 chr2: 3,358,584-3,733,756 , GRCh37.p13 chr2: 3,362,355-3,781,346 RNASEH1, TRAPPC12, 11 more genes
    nsv4728726copy number variation1nstd102humanUncertain significance GRCh37 chr2: 2,529,149-5,511,339 , GRCh38.p12 chr2: 2,525,377-5,371,206 LOC107985840, COLEC11, 24 more genes
    nsv4728695copy number variation1nstd102humanUncertain significance GRCh37 chr2: 3,385,474-4,974,948 , GRCh38.p12 chr2: 3,381,703-4,927,358 LOC105373397, LOC105373394, 17 more genes
    nsv4728621copy number variation1nstd102humanPathogenic GRCh37 chr2: 2,074,335-3,934,366 , GRCh38.p12 chr2: 2,070,563-3,886,776 LOC105373389, MYT1L, 18 more genes
    nsv4674784copy number variation1nstd102humanUncertain significance GRCh37 chr2: 1,045,542-4,104,255 , GRCh38.p12 chr2: 1,049,856-4,056,664 LOC105373390, MYT1L-AS1, 27 more genes
    nsv4519712copy number variation1nstd166human GRCh37.p13 chr2: 3,584,583-3,585,822 , GRCh38.p12 chr2: 3,536,993-3,538,232 RNASEH1
    nsv4454966copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,770-7,502,796 , GRCh38.p12 chr2: 12,770-7,362,665 LINC01810, ADI1, 83 more genes
    nsv4452632copy number variation1nstd102humanUncertain significance GRCh37 chr2: 12,770-3,819,558 , GRCh38.p12 chr2: 12,770-3,771,968 LOC107985838, LOC100996637, 45 more genes
    nsv4057543copy number variation1nstd166human GRCh37.p13 chr2: 3,362,355-3,781,346 , GRCh38.p12 chr2: 3,358,584-3,733,756 ADI1, COLEC11, 11 more genes
    nsv3908677copy number variation1nstd102humanUncertain significance NCBI36 chr2: 2,770-4,344,326 , GRCh37 chr2: 12,770-4,366,451 , GRCh38 chr2: 12,770-4,318,861 LINC01865, EIPR1, 50 more genes
    nsv3908628copy number variation1nstd102humanPathogenic NCBI36 chr2: 20,342-14,924,526 , GRCh37 chr2: 30,342-15,007,075 , GRCh38 chr2: 30,342-14,866,951 RPS7, RPL30P3, 198 more genes
    nsv3908605copy number variation1nstd102humanPathogenic GRCh37 chr2: 66,097-55,797,773 , GRCh38 chr2: 66,097-55,570,637 , NCBI36 chr2: 56,097-55,651,277 SLC35F6, LOC105374458, 801 more genes
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