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Items: 16

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    Number of Variants: 16

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3913446copy number variation1nstd102humanUncertain significance NCBI36 chr6: 33,491,109-33,508,684 , GRCh38 chr6: 33,415,354-33,432,929 , GRCh37 chr6: 33,383,131-33,400,706 PHF1, CUTA, 1 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 PHF1, LOC105378061, 2914 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 PHF1, RNU6-411P, 2910 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 PHF1, SOD1P1, 2905 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 PHF1, ITPR3, 2905 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 PHF1, HLA-DPB2, 1001 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 PHF1, TRR-ACG1-2, 1385 more genes
    nsv4768386copy number variation1nstd102humanLikely pathogenic GRCh38.p12 chr6: 33,375,382-33,468,170 , NCBI36 chr6: 33,451,137-33,543,925 , GRCh37.p13 chr6: 33,343,159-33,435,947 , GRCh37.p13 chr6|NT_167249.1: 4,836,050-4,916,187 , GRCh38.p12 chr6|NT_167249.2: 4,836,753-4,916,889 PHF1, KIFC1, 6 more genes
    nsv4675941copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 31,036,397-34,088,832 , GRCh38.p12 chr6: 31,068,620-34,121,055 PHF1, AGER, 217 more genes
    nsv7097426copy number variation1nstd102humanUncertain significance GRCh37 chr6: 30,695,893-36,953,949 , GRCh38.p12 chr6: 30,728,116-36,986,173 PHF1, LEMD2, 321 more genes
    nsv7098787copy number variation1nstd102humanUncertain significance GRCh37 chr6: 32,148,920-36,953,949 , GRCh38.p12 chr6: 32,181,143-36,986,173 PHF1, CUTA, 184 more genes
    nsv6313582copy number variation1nstd102humanUncertain significance GRCh37 chr6: 33,069,892-33,751,391 , GRCh38.p12 chr6: 33,102,115-33,783,614 PHF1, LOC107986537, 46 more genes
    nsv4451881copy number variation1nstd102humanUncertain significance GRCh37 chr6: 33,131,435-33,419,703 , GRCh38 chr6: 33,163,658-33,451,926 PHF1, COL11A2, 29 more genes
    nsv4683878copy number variation1nstd102humanUncertain significance GRCh37 chr6: 33,359,763-33,640,005 , GRCh38.p12 chr6: 33,391,986-33,672,228 PHF1, ITPR3-AS1, 12 more genes
    nsv4682849copy number variation1nstd102humanUncertain significance GRCh37 chr6: 33,141,458-33,419,703 , GRCh38.p12 chr6: 33,173,681-33,451,926 PHF1, RPL35AP4, 29 more genes
    nsv1398488copy number variation1nstd102humanUncertain significance GRCh37 chr6: 33,256,191-33,400,523 , GRCh38.p12 chr6: 33,288,414-33,432,746 PHF1, ZBTB22, 14 more genes
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