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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
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7074988inversion1nstd229human GRCh38 chr15: 72,092,532-72,194,070 , GRCh37.p13 chr15: 72,384,873-72,486,411 GRAMD2A, MYO9A, 2 more genes
    nsv7070270inversion1nstd229human GRCh38 chr15: 70,870,846-78,233,029 , GRCh37.p13 chr15: 71,163,185-78,525,371 GOLGA6C, LOC102723657, 178 more genes
    nsv7069747inversion1nstd229human GRCh38 chr15: 65,994,863-75,247,978 , GRCh37.p13 chr15: 66,287,201-75,540,319 REC114, PARP6, 199 more genes
    nsv7069690inversion1nstd229human GRCh38 chr15: 72,171,327-72,175,178 , GRCh37.p13 chr15: 72,463,668-72,467,519 GRAMD2A
    nsv7059031inversion1nstd229human GRCh38 chr15: 70,160,153-73,809,878 , GRCh37.p13 chr15: 70,452,492-74,102,219 CD276, LOC107984716, 71 more genes
    nsv6976507copy number variation1nstd229human GRCh38 chr15: 72,181,429-72,185,493 , GRCh37.p13 chr15: 72,473,770-72,477,834 GRAMD2A
    nsv6976501copy number variation1nstd229human GRCh38 chr15: 72,179,166-72,185,491 , GRCh37.p13 chr15: 72,471,507-72,477,832 GRAMD2A
    nsv6975504copy number variation1nstd229human GRCh38 chr15: 72,171,326-72,178,559 , GRCh37.p13 chr15: 72,463,667-72,470,900 GRAMD2A
    nsv6974336copy number variation1nstd229human GRCh38 chr15: 72,156,187-72,159,678 , GRCh37.p13 chr15: 72,448,528-72,452,019 GRAMD2A
    nsv6971511copy number variation1nstd229human GRCh38 chr15: 72,162,956-72,200,644 , GRCh37.p13 chr15: 72,455,297-72,492,985 GRAMD2A, PKM
    nsv6963537copy number variation1nstd229human GRCh38 chr15: 72,159,478-72,159,516 , GRCh37.p13 chr15: 72,451,819-72,451,857 GRAMD2A
    nsv6637443copy number variation1nstd102humanUncertain significance GRCh37 chr15: 72,438,858-72,487,897 , GRCh38.p12 chr15: 72,146,517-72,195,556 GRAMD2A
    nsv6592753inversion1nstd223human GRCh38 chr15: 72,188,064-72,188,974 , GRCh37.p13 chr15: 72,480,405-72,481,315 GRAMD2A
    nsv6586023inversion1nstd223human GRCh38 chr15: 72,171,325-72,175,178 , GRCh37.p13 chr15: 72,463,666-72,467,519 GRAMD2A
    nsv6585499inversion1nstd223human GRCh38 chr15: 72,186,349-72,186,924 , GRCh37.p13 chr15: 72,478,690-72,479,265 GRAMD2A
    nsv6514363copy number variation1nstd223human GRCh38 chr15: 72,156,187-72,159,674 , GRCh37.p13 chr15: 72,448,528-72,452,015 GRAMD2A
    nsv6503357copy number variation1nstd223human GRCh38 chr15: 72,143,150-72,196,385 , GRCh37.p13 chr15: 72,435,491-72,488,726 SENP8, GRAMD2A
    nsv6503015copy number variation1nstd223human GRCh38 chr15: 72,171,324-72,178,551 , GRCh37.p13 chr15: 72,463,665-72,470,892 GRAMD2A
    nsv6498609copy number variation1nstd223human GRCh38 chr15: 72,174,296-72,174,722 , GRCh37.p13 chr15: 72,466,637-72,467,063 GRAMD2A
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