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Items: 1 to 20 of 220

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5957524insertion1nstd209human GRCh38 chr1: 11,770,151-11,770,151 , GRCh37.p13 chr1: 11,830,208-11,830,208 C1orf167
    nsv5881118copy number variation1nstd209human GRCh38 chr1: 11,778,681-11,778,792 , GRCh37.p13 chr1: 11,838,738-11,838,849 C1orf167, C1orf167-AS1
    nsv5827732copy number variation1nstd209human GRCh38 chr1: 11,771,456-11,772,602 , GRCh37.p13 chr1: 11,831,513-11,832,659 C1orf167
    nsv5714698mobile element insertion2nstd211human GRCh38 chr1: 11,770,163-11,770,163 , GRCh37.p13 chr1: 11,830,220-11,830,220 C1orf167
    nsv5677056mobile element insertion2nstd211human GRCh38 chr1: 11,770,163-11,770,163 , GRCh37.p13 chr1: 11,830,220-11,830,220 C1orf167
    nsv5614259insertion1nstd207human GRCh38 chr1: 11,770,151-11,770,151 , GRCh37.p13 chr1: 11,830,208-11,830,208 C1orf167
    nsv5561087mobile element insertion1nstd206human GRCh38 chr1: 11,770,163-11,770,214 , GRCh37.p13 chr1: 11,830,220-11,830,271 C1orf167
    nsv5431280copy number variation1nstd206human GRCh38 chr1: 11,758,557-11,761,113 , GRCh37.p13 chr1: 11,818,614-11,821,170 C1orf167, LOC101060126
    nsv5431151copy number variation1nstd206human GRCh38 chr1: 11,788,390-11,788,448 , GRCh37.p13 chr1: 11,848,447-11,848,505 MTHFR, C1orf167
    nsv5353941translocation1nstd200human GRCh38 chr1: 11,785,025-11,785,025 , GRCh38 chr1: 11,785,075-11,785,075 , GRCh37.p13 chr1: 11,845,082-11,845,082 , GRCh37.p13 chr1: 11,845,132-11,845,132 MTHFR, C1orf167
    nsv5198188mobile element insertion1nstd203human GRCh38 chr1: 11,770,116-11,770,163 , GRCh37.p13 chr1: 11,830,173-11,830,220 C1orf167
    nsv5196307mobile element insertion1nstd203human GRCh38 chr1: 11,770,161-11,770,161 , GRCh37.p13 chr1: 11,830,218-11,830,218 C1orf167
    nsv5194710mobile element insertion1nstd203human GRCh38 chr1: 11,770,160-11,770,160 , GRCh37.p13 chr1: 11,830,217-11,830,217 C1orf167
    nsv5193152mobile element insertion1nstd203human GRCh38 chr1: 11,770,153-11,770,163 , GRCh37.p13 chr1: 11,830,210-11,830,220 C1orf167
    nsv5191401mobile element insertion1nstd203human GRCh38 chr1: 11,770,162-11,770,162 , GRCh37.p13 chr1: 11,830,219-11,830,219 C1orf167
    nsv5188646mobile element insertion1nstd203human GRCh38 chr1: 11,770,151-11,770,163 , GRCh37.p13 chr1: 11,830,208-11,830,220 C1orf167
    nsv5183357mobile element insertion1nstd203human GRCh38 chr1: 11,770,163-11,770,163 , GRCh37.p13 chr1: 11,830,220-11,830,220 C1orf167
    nsv5075720mobile element insertion1nstd203human GRCh38 chr1: 11,773,774-11,773,786 , GRCh37.p13 chr1: 11,833,831-11,833,843 C1orf167
    nsv5062982mobile element insertion1nstd203human GRCh38 chr1: 11,760,660-11,760,710 , GRCh37.p13 chr1: 11,820,717-11,820,767 C1orf167, LOC101060126
    nsv4889914copy number variation1nstd200human GRCh38 chr1: 11,770,537-11,771,415 , GRCh37.p13 chr1: 11,830,594-11,831,472 C1orf167
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