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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137025copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 43,891,760-43,900,060 , GRCh38.p12 chr15: 43,599,562-43,607,862 CKMT1B, STRC, 1 more genes
    nsv7093388copy number variation1nstd102humanPathogenic GRCh37 chr15: 43,888,606-43,941,032 , GRCh38.p12 chr15: 43,596,408-43,648,834 CKMT1B, CATSPER2, 5 more genes
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv6975170copy number variation1nstd229human GRCh38 chr15: 43,479,701-43,751,300 , GRCh37.p13 chr15: 43,771,899-44,043,498 CKMT1B, PPIP5K1P1-CATSPER2, 15 more genes
    nsv6635943copy number variation1nstd227human GRCh38.p12 chr15: 43,544,751-43,647,444 , GRCh37 chr15: 43,836,949-43,939,642 CKMT1B, PPIP5K1, 6 more genes
    nsv6623256copy number variation41nstd224human GRCh37 chr15: 43,890,409-43,939,659 , GRCh38.p12 chr15: 43,598,211-43,647,461 CKMT1B, CATSPER2, 5 more genes
    nsv6623255copy number variation2nstd224human GRCh37 chr15: 43,890,409-43,939,642 , GRCh38.p12 chr15: 43,598,211-43,647,444 CKMT1B, CATSPER2, 5 more genes
    nsv6623254copy number variation3nstd224human GRCh37 chr15: 43,851,025-43,939,659 , GRCh38.p12 chr15: 43,558,827-43,647,461 CKMT1B, PPIP5K1, 6 more genes
    nsv6623086copy number variation1nstd224human GRCh37 chr15: 43,851,025-43,990,212 , GRCh38.p12 chr15: 43,558,827-43,698,014 STRC, PPIP5K1P1, 9 more genes
    nsv6622893copy number variation1nstd224human GRCh37 chr15: 43,890,409-43,939,569 , GRCh38.p12 chr15: 43,598,211-43,647,371 CKMT1B, CATSPER2, 5 more genes
    nsv6505647copy number variation1nstd223human GRCh38 chr15: 43,596,201-43,599,300 , GRCh37.p13 chr15: 43,888,399-43,891,498 STRC, CKMT1B
    nsv6496110copy number variation1nstd223human GRCh38 chr15: 43,175,921-43,650,339 , GRCh37.p13 chr15: 43,468,119-43,942,537 ADAL, EPB42, 19 more genes
    nsv6291560copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,215,243-44,632,384 , GRCh38.p12 chr15: 42,923,045-44,340,186 PPIP5K1P1-CATSPER2, STRCP1, 44 more genes
    nsv6290550copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 43,891,870-43,901,474 , GRCh38 chr15: 43,599,672-43,609,276 CKMT1B, STRC, 1 more genes
    nsv6290205copy number variation1nstd102humanPathogenic GRCh37 chr15: 43,851,199-43,924,279 , GRCh38.p12 chr15: 43,559,001-43,632,081 CKMT1B, PPIP5K1, 4 more genes
    nsv6290201copy number variation1nstd102humanPathogenic GRCh37 chr15: 43,851,199-44,038,820 , GRCh38.p12 chr15: 43,559,001-43,746,622 CATSPER2P1, CKMT1A, 13 more genes
    nsv6290131copy number variation2nstd102humanPathogenic, Likely pathogenic GRCh37 chr15: 43,851,199-44,038,794 , GRCh38.p12 chr15: 43,559,001-43,746,596 STRCP1, CKMT1B, 13 more genes
    nsv6137697copy number variation1nstd102humanBenign GRCh37 chr15: 43,891,596-44,010,458 , GRCh38.p12 chr15: 43,599,398-43,718,260 STRC, CATSPER2, 9 more genes
    nsv6122608copy number variation1nstd186human GRCh37 chr15: 43,891,072-43,902,072 , GRCh38.p12 chr15: 43,598,874-43,609,874 CKMT1B, STRC, 1 more genes
    nsv6120590copy number variation1nstd186human GRCh37 chr15: 43,888,635-43,957,072 , GRCh38.p12 chr15: 43,596,437-43,664,874 CKMT1B, CATSPER2, 6 more genes
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