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Items: 17

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    Number of Variants: 17

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 CCNJ, RNU7-12P, 1876 more genes
    nsv3920295copy number variation1nstd102humanPathogenic NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422 CCNJ, EIF2S2P3, 895 more genes
    nsv3911437copy number variation1nstd102humanPathogenic GRCh38 chr10: 93,181,201-101,356,779 , NCBI36 chr10: 94,930,948-103,106,526 , GRCh37 chr10: 94,940,958-103,116,536 CCNJ, SLF2, 171 more genes
    nsv3894877copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,908,171-101,809,723 , GRCh38.p12 chr10: 92,148,414-100,049,966 CCNJ, RNY3P12, 146 more genes
    nsv3908115copy number variation1nstd102humanPathogenic GRCh37 chr10: 92,667,881-98,970,384 , GRCh38.p12 chr10: 90,908,124-97,210,627 CCNJ, EXOC6, 118 more genes
    nsv3912487copy number variation1nstd102humanPathogenic GRCh37 chr10: 94,386,437-99,514,859 , GRCh38 chr10: 92,626,680-97,755,102 , NCBI36 chr10: 94,376,417-99,504,849 CCNJ, ENTPD1-AS1, 105 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 CCNJ, LOC100419870, 2105 more genes
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 CCNJ, AGAP14P, 2097 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 CCNJ, ANXA11, 2085 more genes
    nsv3891958copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414 CCNJ, TUBB8, 2085 more genes
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 CCNJ, EXOC6, 1906 more genes
    nsv3905489copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,283,493-135,427,143 , GRCh38.p12 chr10: 91,523,736-133,613,639 CCNJ, LOC105378476, 688 more genes
    nsv3890046copy number variation1nstd102humanPathogenic GRCh37 chr10: 94,346,520-135,427,143 , GRCh38.p12 chr10: 92,586,763-133,613,639 CCNJ, UROS, 667 more genes
    nsv3909942copy number variation1nstd102humanPathogenic GRCh37 chr10: 96,872,364-118,383,651 , GRCh38 chr10: 95,112,607-116,776,637 , NCBI36 chr10: 96,862,354-118,526,138 CCNJ, LOC102723665, 360 more genes
    nsv3907664copy number variation1nstd102humandrug response GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422 CCNJ, SHOC2, 1487 more genes
    nsv3894450copy number variation1nstd102humandrug response GRCh37 chr10: 85,557,432-105,804,295 , GRCh38.p12 chr10: 83,797,676-104,044,537 CCNJ, HPS1, 422 more genes
    nsv5564286copy number variation1nstd102humanUncertain significance GRCh37 chr10: 97,366,499-98,031,175 , GRCh38.p12 chr10: 95,606,742-96,271,418 CCNJ, ENTPD1-AS1, 10 more genes
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