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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053948inversion1nstd229human GRCh38 chr2: 236,325,891-239,580,552 , GRCh37.p13 chr2: 237,234,534-240,502,246 PER2, MIR4269, 60 more genes
    nsv7047549inversion1nstd229human GRCh38 chr2: 236,010,287-240,118,231 , GRCh37.p13 chr2: 236,918,931-241,057,648 RAB17, COL6A3, 74 more genes
    nsv6714884copy number variation1nstd229human GRCh38 chr2: 236,201,423-237,051,295 , GRCh37.p13 chr2: 237,110,066-237,959,938 LOC105373945, LOC105373948, 13 more genes
    nsv6713826copy number variation1nstd229human GRCh38 chr2: 237,001,084-237,071,458 , GRCh37.p13 chr2: 237,909,727-237,980,101 LOC105373950, LOC93463, 1 more genes
    nsv6709621copy number variation1nstd229human GRCh38 chr2: 236,972,309-237,013,507 , GRCh37.p13 chr2: 237,880,952-237,922,150 RNU6-1051P, COPS8-DT
    nsv6709283copy number variation1nstd229human GRCh38 chr2: 236,031,460-237,450,881 , GRCh37.p13 chr2: 236,940,104-238,359,524 GBX2, LOC105373945, 22 more genes
    nsv6702837copy number variation1nstd229human GRCh38 chr2: 236,823,646-237,035,457 , GRCh37.p13 chr2: 237,732,289-237,944,100 COPS8-DT, RNU6-1051P
    nsv6701870copy number variation1nstd229human GRCh38 chr2: 235,899,114-238,770,175 , GRCh37.p13 chr2: 236,807,758-239,678,816 RN7SL204P, RBM44, 55 more genes
    nsv6636841copy number variation1nstd102humanPathogenic GRCh37 chr2: 236,878,509-242,783,384 , GRCh38.p12 chr2: 235,969,865-241,841,232 COPS8-DT, MTND5P46, 128 more genes
    nsv6636673copy number variation1nstd102humanPathogenic GRCh37 chr2: 235,942,616-242,783,384 , GRCh38.p12 chr2: 235,033,972-241,841,232 LINC02991, OR6B3, 136 more genes
    nsv6315457copy number variation1nstd102humanPathogenic GRCh37 chr2: 236,472,789-242,783,384 , GRCh38.p12 chr2: 235,564,145-241,841,232 AGAP1, OR5S1P, 130 more genes
    nsv6315436copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,227,837-242,783,384 , GRCh38.p12 chr2: 232,363,127-241,841,232 LOC105373929, LOC105373932, 204 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314846copy number variation1nstd102humanPathogenic GRCh38 chr2: 236,710,422-242,106,504 , GRCh37.p13 chr2: 237,619,065-243,048,655 LINC01937, FAM240C, 126 more genes
    nsv6313668copy number variation1nstd102humanPathogenic GRCh37 chr2: 219,606,537-239,217,703 , GRCh38.p12 chr2: 218,741,814-238,309,062 LOC105373947, RN7SL764P, 357 more genes
    nsv6311563copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr2: 236,403,331-242,801,596 , GRCh38.p12 chr2: 235,494,687-241,859,444 HDAC4-AS1, COPS8-DT, 134 more genes
    nsv6291434copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,499,041-242,783,384 , GRCh38.p12 chr2: 236,590,398-241,841,232 LINC01107, COL6A3, 118 more genes
    nsv5673218copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,481,970-238,305,470 , GRCh38.p12 chr2: 236,573,327-237,396,827 LOC105373946, LOC105373949, 13 more genes
    nsv5381323copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,201,756-243,048,760 , GRCh38.p12 chr2: 236,293,113-242,106,609 LRRFIP1, GPR35, 133 more genes
    nsv5318856copy number variation1nstd204human GRCh38.p13 chr2: 236,094,899-237,206,460 , GRCh37.p13 chr2: 237,003,543-238,115,103 , LOC105373948, 20 more genes
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