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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095431copy number variation1nstd102humanUncertain significance GRCh37 chr18: 18,963,480-21,534,612 , GRCh38.p12 chr18: 21,383,519-23,954,648 MIB1, RN7SL233P, 41 more genes
    nsv7017898copy number variation1nstd229human GRCh38 chr18: 21,630,828-21,630,933 , GRCh37.p13 chr18: 19,210,789-19,210,894 SNRPD1
    nsv7003998copy number variation1nstd229human GRCh38 chr18: 21,602,498-21,611,048 , GRCh37.p13 chr18: 19,182,459-19,191,009 SNRPD1
    nsv7003940copy number variation1nstd229human GRCh38 chr18: 21,615,075-21,680,891 , GRCh37.p13 chr18: 19,195,036-19,260,852 ABHD3, SNRPD1
    nsv7003860copy number variation1nstd229human GRCh38 chr18: 21,618,557-21,619,188 , GRCh37.p13 chr18: 19,198,518-19,199,149 SNRPD1
    nsv6595127inversion1nstd223human GRCh38 chr18: 21,615,240-21,616,343 , GRCh37.p13 chr18: 19,195,201-19,196,304 SNRPD1
    nsv6587981inversion1nstd223human GRCh38 chr18: 21,630,764-21,631,141 , GRCh37.p13 chr18: 19,210,725-19,211,102 SNRPD1
    nsv6577865inversion1nstd223human GRCh38 chr18: 21,620,997-21,621,467 , GRCh37.p13 chr18: 19,200,958-19,201,428 SNRPD1
    nsv6522212copy number variation1nstd223human GRCh38 chr18: 21,620,028-21,621,651 , GRCh37.p13 chr18: 19,199,989-19,201,612 SNRPD1
    nsv6516012copy number variation1nstd223human GRCh38 chr18: 21,633,989-21,638,809 , GRCh37.p13 chr18: 19,213,950-19,218,770 SNRPD1
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 more genes
    nsv6291786copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-25,252,276 , GRCh38.p12 chr18: 136,226-27,672,312 LOC107985122, LOC100130487, 375 more genes
    nsv6291540copy number variation1nstd102humanUncertain significance GRCh37 chr18: 18,611,942-26,843,691 , GRCh38.p12 chr18: 21,031,981-29,263,726 MIR133A1HG, LOC105372040, 111 more genes
    nsv6039171copy number variation1nstd212human GRCh38 chr18: 21,619,672-21,619,733 , GRCh37.p13 chr18: 19,199,633-19,199,694 SNRPD1
    nsv5375125translocation1nstd200human GRCh38 chr18: 21,633,127-21,633,127 , GRCh38 chr18: 21,595,317-21,595,317 , GRCh37.p13 chr18: 19,175,278-19,175,278 , GRCh37.p13 chr18: 19,213,088-19,213,088 SNRPD1, ESCO1
    nsv5031658inversion1nstd200human GRCh38 chr18: 21,621,237-21,621,626 , GRCh37.p13 chr18: 19,201,198-19,201,587 SNRPD1
    nsv5026864copy number variation1nstd200human GRCh38 chr18: 21,631,531-21,633,131 , GRCh37.p13 chr18: 19,211,492-19,213,092 SNRPD1
    nsv4633726copy number variation1nstd183human GRCh37 chr18: 19,203,915-19,222,345 , GRCh38.p12 chr18: 21,623,954-21,642,384 SNRPD1
    nsv4627049copy number variation1nstd183human GRCh37 chr18: 19,203,983-19,210,429 , GRCh38.p12 chr18: 21,624,022-21,630,468 SNRPD1
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