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Items: 1 to 20 of 203

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966054insertion1nstd209human GRCh38 chr1: 12,183,817-12,183,817 , GRCh37.p13 chr1: 12,243,874-12,243,874 TNFRSF1B
    nsv5883335copy number variation1nstd209human GRCh38 chr1: 12,174,139-12,174,189 , GRCh37.p13 chr1: 12,234,196-12,234,246 TNFRSF1B
    nsv5619552insertion1nstd207human GRCh38 chr1: 12,174,154-12,174,154 , GRCh37.p13 chr1: 12,234,211-12,234,211 TNFRSF1B
    nsv5578790copy number variation1nstd207human GRCh38 chr1: 12,174,139-12,174,195 , GRCh37.p13 chr1: 12,234,196-12,234,252 TNFRSF1B
    nsv5432536copy number variation1nstd206human GRCh38 chr1: 12,204,024-12,205,349 , GRCh37.p13 chr1: 12,264,081-12,265,406 TNFRSF1B
    nsv5431646copy number variation1nstd206human GRCh38 chr1: 12,192,097-12,205,344 , GRCh37.p13 chr1: 12,252,154-12,265,401 TNFRSF1B, MIR4632
    nsv5421750copy number variation1nstd206human GRCh38 chr1: 12,178,722-12,185,188 , GRCh37.p13 chr1: 12,238,779-12,245,245 TNFRSF1B
    nsv5354026translocation1nstd200human GRCh38 chr1: 12,204,024-12,204,024 , GRCh38 chr1: 12,205,349-12,205,349 , GRCh37.p13 chr1: 12,264,081-12,264,081 , GRCh37.p13 chr1: 12,265,406-12,265,406 TNFRSF1B
    nsv5202824copy number variation1nstd204human GRCh38.p13 chr1: 12,136,601-12,213,100 , GRCh37.p13 chr1: 12,196,658-12,273,157 , MIR7846, 3 more genes
    nsv5191563mobile element insertion1nstd203human GRCh38 chr1: 12,183,245-12,183,254 , GRCh37.p13 chr1: 12,243,302-12,243,311 TNFRSF1B
    nsv4903076copy number variation1nstd200human GRCh38 chr1: 12,192,097-12,205,344 , GRCh37.p13 chr1: 12,252,154-12,265,401 MIR4632, TNFRSF1B
    nsv4889930copy number variation1nstd200human GRCh38 chr1: 12,169,155-12,169,222 , GRCh37.p13 chr1: 12,229,212-12,229,279 TNFRSF1B
    nsv4593845copy number variation1nstd183human GRCh37 chr1: 12,200,036-12,238,310 , GRCh38.p12 chr1: 12,139,979-12,178,253 TNFRSF8, MIR7846, 1 more genes
    nsv4593844copy number variation1nstd183human GRCh37 chr1: 12,181,729-12,256,122 , GRCh38.p12 chr1: 12,121,672-12,196,065 TNFRSF8, MIR7846, 2 more genes
    nsv4579138copy number variation1nstd183human GRCh37 chr1: 12,227,018-12,227,220 , GRCh38.p12 chr1: 12,166,961-12,167,163 TNFRSF1B, MIR7846
    nsv4516555copy number variation1nstd166human GRCh37.p13 chr1: 12,251,507-12,251,589 , GRCh38.p12 chr1: 12,191,450-12,191,532 TNFRSF1B, MIR4632
    nsv4454705copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,246,640-12,841,900 , GRCh38.p12 chr1: 10,186,582-12,781,757 LINC01647, MIR7846, 73 more genes
    nsv4436711copy number variation1nstd102humanPathogenic GRCh37 chr1: 11,794,553-12,786,444 , GRCh38.p12 chr1: 11,734,496-12,726,477 MIR4632, AADACL3, 31 more genes
    nsv4436680complex substitution1nstd102humanUncertain significance GRCh38.p12 chr1: 973,858-24,379,779 , GRCh37 chr1: 909,238-24,706,269 ALPL, RERE, 636 more genes
    nsv4436526complex substitution1nstd102humanUncertain significance GRCh38.p12 chr1: 973,858-16,409,637 , GRCh37 chr1: 909,238-16,736,132 RERE, CA6, 415 more genes
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