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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
    nsv7046600inversion1nstd229human GRCh38 chr2: 237,108,675-239,672,919 , GRCh37.p13 chr2: 238,017,318-240,594,613 RBM44, MIR4440, 46 more genes
    nsv6716675copy number variation1nstd229human GRCh38 chr2: 237,569,991-237,590,930 , GRCh37.p13 chr2: 238,478,634-238,499,573 RAB17, RAB17-DT
    nsv6714372copy number variation1nstd229human GRCh38 chr2: 237,566,060-237,602,719 , GRCh37.p13 chr2: 238,474,703-238,511,362 RAB17, RAB17-DT, 1 more genes
    nsv6713877copy number variation1nstd229human GRCh38 chr2: 237,105,873-237,623,710 , GRCh37.p13 chr2: 238,014,516-238,532,353 PRLH, LOC105373953, 9 more genes
    nsv6704328copy number variation1nstd229human GRCh38 chr2: 237,340,674-237,738,012 , GRCh37.p13 chr2: 238,249,317-238,646,655 PRLH, RNU6-1140P, 8 more genes
    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
    nsv6699858copy number variation1nstd229human GRCh38 chr2: 237,554,560-237,656,007 , GRCh37.p13 chr2: 238,463,203-238,564,650 RAB17-DT, MLPH, 4 more genes
    nsv6698955copy number variation1nstd229human GRCh38 chr2: 237,593,000-237,593,189 , GRCh37.p13 chr2: 238,501,643-238,501,832 RAB17-DT
    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
    nsv6627645copy number variation1nstd224human GRCh37 chr2: 238,249,550-238,643,972 , GRCh38.p12 chr2: 237,340,907-237,735,329 LRRFIP1, MIR6811, 8 more genes
    nsv6627569copy number variation1nstd224human GRCh37 chr2: 238,249,370-238,643,972 , GRCh38.p12 chr2: 237,340,727-237,735,329 COL6A3, MIR6811, 8 more genes
    nsv6336535copy number variation1nstd223human GRCh38 chr2: 237,593,000-237,593,189 , GRCh37.p13 chr2: 238,501,643-238,501,832 RAB17-DT
    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
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