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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5279775copy number variation1nstd204human GRCh38.p13 chr15: 72,663,301-72,665,000 , GRCh37.p13 chr15: 72,955,642-72,957,341 RN7SL853P, GOLGA6B
    nsv5279545copy number variation1nstd204human GRCh38.p13 chr15: 72,657,501-72,662,200 , GRCh37.p13 chr15: 72,949,842-72,954,541 GOLGA6B
    nsv5278245copy number variation1nstd204human GRCh38.p13 chr15: 72,652,201-72,653,600 , GRCh37.p13 chr15: 72,944,542-72,945,941 GOLGA6B
    nsv5275780copy number variation1nstd204human GRCh38.p13 chr15: 72,653,801-72,655,900 , GRCh37.p13 chr15: 72,946,142-72,948,241 GOLGA6B
    nsv5275275copy number variation1nstd204human GRCh38.p13 chr15: 72,658,201-72,660,500 , GRCh37.p13 chr15: 72,950,542-72,952,841 GOLGA6B
    nsv5275257copy number variation1nstd204human GRCh38.p13 chr15: 72,661,001-72,663,900 , GRCh37.p13 chr15: 72,953,342-72,956,241 RN7SL853P, GOLGA6B
    nsv5273181copy number variation1nstd204human GRCh38.p13 chr15: 72,661,201-72,667,700 , GRCh37.p13 chr15: 72,953,542-72,960,041 GOLGA6B, RN7SL853P
    nsv5270929copy number variation1nstd204human GRCh38.p13 chr15: 72,664,201-72,664,600 , GRCh37.p13 chr15: 72,956,542-72,956,941 RN7SL853P, GOLGA6B
    nsv5266396copy number variation1nstd204human GRCh38.p13 chr15: 72,665,001-72,670,500 , GRCh37.p13 chr15: 72,957,342-72,962,841 GOLGA6B, RN7SL853P
    nsv5264581copy number variation1nstd204human GRCh38.p13 chr15: 72,663,340-72,664,524 , GRCh37.p13 chr15: 72,955,681-72,956,865 GOLGA6B, RN7SL853P
    nsv5262186copy number variation1nstd204human GRCh38.p13 chr15: 72,662,201-72,662,500 , GRCh37.p13 chr15: 72,954,542-72,954,841 GOLGA6B
    nsv4730060inversion2nstd198human GRCh38 chr15: 72,662,255-72,666,131 , GRCh37.p13 chr15: 72,954,596-72,958,472 GOLGA6B, RN7SL853P
    nsv4728893copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 70,268,937-74,098,081 , GRCh38.p12 chr15: 69,976,598-73,805,740 BBS4, FKBP1AP2, 75 more genes
    nsv4727865copy number variation1nstd197human GRCh38.p12 chr15: 72,661,265-72,664,511 , GRCh37 chr15: 72,953,606-72,956,852 GOLGA6B, RN7SL853P
    nsv4683941copy number variation1nstd102humanUncertain significance GRCh37 chr15: 72,646,022-73,660,621 , GRCh38.p12 chr15: 72,353,681-73,368,280 TMEM202, PHB1P20, 24 more genes
    nsv4638764copy number variation4nstd186human GRCh37 chr15: 72,950,000-72,961,400 , GRCh38.p12 chr15: 72,657,659-72,669,059 GOLGA6B, RN7SL853P
    nsv4627486copy number variation2nstd183human GRCh37 chr15: 72,954,392-72,958,808 , GRCh38.p12 chr15: 72,662,051-72,666,467 RN7SL853P, GOLGA6B
    nsv4626551copy number variation1nstd183human GRCh37 chr15: 72,930,264-72,965,653 , GRCh38.p12 chr15: 72,637,923-72,673,312 RN7SL853P, GOLGA6B, 1 more genes
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