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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6666252copy number variation1nstd229human GRCh38 chr2: 20,432,894-20,530,086 , GRCh37.p13 chr2: 20,632,655-20,729,846 LOC107985856, RHOB, 2 more genes
    nsv6658422copy number variation1nstd229human GRCh38 chr2: 19,749,421-21,263,284 , GRCh37.p13 chr2: 19,949,182-21,486,156 LOC107985856, CISD1P1, 33 more genes
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6350208copy number variation1nstd223human GRCh38 chr2: 20,432,893-20,530,084 , GRCh37.p13 chr2: 20,632,654-20,729,844 LOC102724948, NDUFAF2P1, 2 more genes
    nsv6339857copy number variation1nstd223human GRCh38 chr2: 20,445,896-20,446,132 , GRCh37.p13 chr2: 20,645,657-20,645,893 RHOB
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6151602copy number variation1nstd214human GRCh38 chr2: 20,445,896-20,446,097 , GRCh37.p13 chr2: 20,645,657-20,645,858 RHOB
    nsv6148031copy number variation1nstd214human GRCh38 chr2: 20,445,896-20,445,997 , GRCh37.p13 chr2: 20,645,657-20,645,758 RHOB
    nsv6059819insertion1nstd212human GRCh38 chr2: 20,445,944-20,445,944 , GRCh37.p13 chr2: 20,645,705-20,645,705 RHOB
    nsv6055078insertion1nstd212human GRCh38 chr2: 20,445,997-20,445,997 , GRCh37.p13 chr2: 20,645,758-20,645,758 RHOB
    nsv5987496copy number variation1nstd212human GRCh38 chr2: 20,445,951-20,446,016 , GRCh37.p13 chr2: 20,645,712-20,645,777 RHOB
    nsv5621691insertion1nstd207human GRCh38 chr2: 20,446,087-20,446,087 , GRCh37.p13 chr2: 20,645,848-20,645,848 RHOB
    nsv5576552copy number variation1nstd207human GRCh38 chr2: 20,445,896-20,446,131 , GRCh37.p13 chr2: 20,645,657-20,645,892 RHOB
    nsv4763394insertion1nstd199human GRCh37 chr2: 20,645,713-20,645,713 , GRCh38.p12 chr2: 20,445,952-20,445,952 RHOB
    nsv4674430copy number variation1nstd102humanUncertain significance GRCh37 chr2: 20,576,216-20,684,239 , GRCh38.p12 chr2: 20,376,455-20,484,478 SLC7A15P, RNA5SP86, 3 more genes
    nsv4582812copy number variation1nstd183human GRCh37 chr2: 20,645,569-20,646,079 , GRCh38.p12 chr2: 20,445,808-20,446,318 RHOB
    nsv4451022copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,631,145-21,729,493 , GRCh38.p12 chr2: 15,491,021-21,506,621 RAD51AP2, LOC101928149, 82 more genes
    nsv4409601copy number variation1nstd174human GRCh37 chr2: 20,645,657-20,645,927 , GRCh38.p12 chr2: 20,445,896-20,446,166 RHOB
    nsv4335876sequence alteration1nstd166human GRCh37.p13 chr2: 20,021,666-53,788,063 , GRCh38.p12 chr2: 19,821,905-53,560,926 , ADCY3, 531 more genes
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