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Items: 1 to 20 of 221

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7058136inversion1nstd229human GRCh38 chr12: 29,281,651-29,281,740 , GRCh37.p13 chr12: 29,434,584-29,434,673 LOC100506606, FAR2
    nsv6931058copy number variation1nstd229human GRCh38 chr12: 29,315,898-29,319,261 , GRCh37.p13 chr12: 29,468,831-29,472,194 LOC100506606, FAR2
    nsv6930867copy number variation1nstd229human GRCh38 chr12: 29,275,067-29,285,704 , GRCh37.p13 chr12: 29,428,000-29,438,637 LOC100506606, FAR2
    nsv6929121copy number variation1nstd229human GRCh38 chr12: 29,284,557-29,295,688 , GRCh37.p13 chr12: 29,437,490-29,448,621 LOC100506606, FAR2
    nsv6921687copy number variation1nstd229human GRCh38 chr12: 29,276,762-29,286,241 , GRCh37.p13 chr12: 29,429,695-29,439,174 LOC100506606, FAR2
    nsv6918534copy number variation1nstd229human GRCh38 chr12: 28,759,136-29,359,851 , GRCh37.p13 chr12: 28,912,069-29,512,784 LOC101928735, LOC100506606, 3 more genes
    nsv6637881copy number variation1nstd102humanUncertain significance GRCh37 chr12: 28,911,901-29,518,739 , GRCh38.p12 chr12: 28,758,968-29,365,806 LOC101928735, LOC100506606, 3 more genes
    nsv6473735copy number variation1nstd223human GRCh38 chr12: 29,284,557-29,295,686 , GRCh37.p13 chr12: 29,437,490-29,448,619 FAR2, LOC100506606
    nsv6456440copy number variation1nstd223human GRCh38 chr12: 29,294,605-29,323,692 , GRCh37.p13 chr12: 29,447,538-29,476,625 FAR2, LOC100506606
    nsv6290811copy number variation1nstd102humanPathogenic GRCh37 chr12: 23,693,737-29,545,102 , GRCh38.p12 chr12: 23,540,803-29,392,169 LOC105369709, REP15, 74 more genes
    nsv6192026copy number variation1nstd214human GRCh38 chr12: 29,295,714-29,295,823 , GRCh37.p13 chr12: 29,448,647-29,448,756 FAR2, LOC100506606
    nsv6132691copy number variation1nstd213human GRCh37 chr12: 29,430,000-30,280,001 , GRCh38.p12 chr12: 29,277,067-30,127,068 ERGIC2, FAR2, 8 more genes
    nsv6132422copy number variation1nstd213human GRCh37 chr12: 190,000-30,830,001 , GRCh38.p12 chr12: 80,834-30,677,067 , A2M, 622 more genes
    nsv6132171copy number variation1nstd213human GRCh37 chr12: 29,230,000-29,630,001 , GRCh38.p12 chr12: 29,077,067-29,477,068 ERGIC2, FAR2, 3 more genes
    nsv6132170copy number variation1nstd213human GRCh37 chr12: 29,160,000-29,620,001 , GRCh38.p12 chr12: 29,007,067-29,467,068 ERGIC2, FAR2, 4 more genes
    nsv5307114copy number variation1nstd204human GRCh38.p13 chr12: 27,543,878-29,812,093 , GRCh37.p13 chr12: 27,696,811-29,965,026 , RNU4-54P, 28 more genes
    nsv5271040copy number variation1nstd204human GRCh38.p13 chr12: 28,650,801-29,812,400 , GRCh37.p13 chr12: 28,803,734-29,965,333 LOC105369711, ERGIC2, 8 more genes
    nsv5127002mobile element insertion1nstd203human GRCh38 chr12: 29,295,733-29,295,779 , GRCh37.p13 chr12: 29,448,666-29,448,712 LOC100506606, FAR2
    nsv4981759copy number variation1nstd200human GRCh38 chr12: 29,294,603-29,323,691 , GRCh37.p13 chr12: 29,447,536-29,476,624 LOC100506606, FAR2
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