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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4729684copy number variation1nstd102humanUncertain significance GRCh37 chr10: 18,313,841-18,388,434 , GRCh38.p12 chr10: 18,024,912-18,099,505 SLC39A12
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 SLC39A12, RNU7-12P, 1876 more genes
    nsv3914771copy number variation1nstd102humanPathogenic GRCh38 chr10: 54,086-19,336,980 , NCBI36 chr10: 90,026-19,665,915 , GRCh37 chr10: 100,026-19,625,909 SLC39A12, COX6CP17, 302 more genes
    nsv3884983copy number variation1nstd102humanPathogenic GRCh37 chr10: 4,689,760-19,120,882 , GRCh38.p12 chr10: 4,647,568-18,831,953 SLC39A12, HSPA14, 228 more genes
    nsv3911783copy number variation1nstd102humanPathogenic NCBI36 chr10: 7,510,738-21,916,687 , GRCh37 chr10: 7,470,732-21,876,681 , GRCh38 chr10: 7,428,770-21,587,752 SLC39A12, LOC101928834, 192 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 SLC39A12, LOC100419870, 2105 more genes
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 SLC39A12, AGAP14P, 2097 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 SLC39A12, ANXA11, 2085 more genes
    nsv3891958copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414 SLC39A12, TUBB8, 2085 more genes
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 SLC39A12, EXOC6, 1906 more genes
    nsv3904390copy number variation1nstd102humanPathogenic GRCh37 chr10: 100,026-50,961,640 , GRCh38.p12 chr10: 54,086-49,753,594 SLC39A12, LINC00700, 806 more genes
    nsv3920796copy number variation1nstd102humanPathogenic NCBI36 chr10: 62,842-35,729,127 , GRCh37.p13 chr10: 72,842-35,689,121 , GRCh38.p12 chr10: 26,906-35,400,193 SLC39A12, EPC1-AS1, 559 more genes
    nsv6313952copy number variation1nstd102humanPathogenic GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593 SLC39A12, RPL36AP55, 418 more genes
    nsv3917667copy number variation1nstd102humanPathogenic GRCh37 chr10: 224,406-26,628,907 , GRCh38 chr10: 90,205-26,339,978 , NCBI36 chr10: 126,145-26,668,913 SLC39A12, RN7SKP241, 389 more genes
    nsv3924406copy number variation1nstd102humanPathogenic GRCh38 chr10: 69,261-19,184,047 , GRCh37 chr10: 224,406-19,472,976 , NCBI36 chr10: 105,201-19,512,982 SLC39A12, WDR37, 302 more genes
    nsv3920598copy number variation1nstd102humanBenign NCBI36 chr10: 4,636,926-47,125,152 , GRCh38 chr10: 4,604,734-48,074,662 , GRCh37 chr10: 4,646,926-47,531,169 SLC39A12, LOC100420467, 709 more genes
    nsv3902225copy number variation1nstd102humanUncertain significance GRCh37 chr10: 15,966,534-19,063,585 , GRCh38.p12 chr10: 15,924,535-18,774,656 SLC39A12, CACNB2, 29 more genes
    nsv3902014copy number variation1nstd102humanUncertain significance GRCh37 chr10: 17,766,249-18,867,108 , GRCh38.p12 chr10: 17,724,250-18,578,179 SLC39A12, LOC107984213, 6 more genes
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 SLC39A12, C1QL3, 774 more genes
    nsv3903354copy number variation1nstd102humanUncertain significance GRCh37 chr10: 16,624,071-19,846,248 , GRCh38.p12 chr10: 16,582,072-19,557,319 SLC39A12, ST8SIA6-AS1, 29 more genes
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