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Items: 19

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    Number of Variants: 19

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3899854copy number variation1nstd102humanLikely benign GRCh37 chr10: 75,010,521-75,011,564 , GRCh38.p12 chr10: 73,250,763-73,251,806 DNAJC9-AS1, CFAP70, 1 more genes
    nsv3898911copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,010,165-75,013,328 , GRCh38.p12 chr10: 73,250,407-73,253,570 CFAP70, DNAJC9-AS1, 1 more genes
    nsv6308930copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,010,610-75,012,240 , GRCh38.p12 chr10: 73,250,852-73,252,482 DNAJC9-AS1, MRPS16, 1 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 DNAJC9, RNU7-12P, 1876 more genes
    nsv3922335copy number variation1nstd102humanPathogenic GRCh37 chr10: 60,196,226-76,174,974 , GRCh38 chr10: 58,436,466-74,415,216 , NCBI36 chr10: 59,866,232-75,844,980 DNAJC9, UNC5B-AS1, 250 more genes
    nsv3917822copy number variation1nstd102humanPathogenic GRCh38 chr10: 63,402,579-75,296,099 , GRCh37 chr10: 65,162,339-77,055,857 , NCBI36 chr10: 64,832,345-76,725,863 DNAJC9, MYL6P3, 220 more genes
    nsv6314185copy number variation1nstd102humanPathogenic GRCh37 chr10: 68,735,254-78,885,714 , GRCh38.p12 chr10: 66,975,496-77,125,956 DNAJC9, SLC25A16, 204 more genes
    nsv3910545copy number variation1nstd102humanPathogenic NCBI36 chr10: 74,150,392-77,042,138 , GRCh38 chr10: 72,720,628-75,612,374 , GRCh37 chr10: 74,480,386-77,372,132 DNAJC9, CAMK2G, 73 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 DNAJC9, LOC100419870, 2105 more genes
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 DNAJC9, AGAP14P, 2097 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 DNAJC9, ANXA11, 2085 more genes
    nsv3891958copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414 DNAJC9, TUBB8, 2085 more genes
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 DNAJC9, EXOC6, 1906 more genes
    nsv3924859copy number variation1nstd102humanPathogenic NCBI36 chr10: 52,159,133-88,896,941 , GRCh38 chr10: 50,729,367-87,147,204 , GRCh37 chr10: 52,489,127-88,906,961 DNAJC9, BMS1P4-AGAP5, 471 more genes
    nsv3917047copy number variation1nstd102humanPathogenic NCBI36 chr10: 42,500,760-75,145,672 , GRCh37 chr10: 43,180,754-75,475,666 , GRCh38 chr10: 42,685,306-73,715,908 DNAJC9, SLC9A3P3, 476 more genes
    nsv3891070copy number variation1nstd102humanPathogenic GRCh37 chr10: 69,040,366-93,194,993 , GRCh38.p12 chr10: 67,280,608-91,435,236 DNAJC9, NRG3-AS1, 441 more genes
    nsv3917966copy number variation1nstd102humanPathogenic NCBI36 chr10: 68,626,331-80,851,819 , GRCh37 chr10: 68,956,325-81,181,813 , GRCh38 chr10: 67,196,567-79,422,057 DNAJC9, LINC02640, 231 more genes
    nsv3907664copy number variation1nstd102humandrug response GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422 DNAJC9, SHOC2, 1487 more genes
    nsv6314136copy number variation1nstd102humanUncertain significance GRCh37 chr10: 74,472,028-75,007,588 , GRCh38.p12 chr10: 72,712,270-73,247,830 DNAJC9, MCU, 14 more genes
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