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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148095copy number variation1nstd102humanUncertain significance GRCh37 chr12: 121,341,598-124,103,434 , GRCh38.p12 chr12: 120,903,795-123,618,887 ANAPC5, MLXIP, 82 more genes
    nsv7094203copy number variation1nstd102humanUncertain significance GRCh37 chr12: 122,277,634-124,242,579 , GRCh38.p12 chr12: 121,839,728-123,758,032 SBNO1, MIR9902-1, 58 more genes
    nsv7075012inversion1nstd229human GRCh38 chr12: 123,447,272-123,623,119 , GRCh37.p13 chr12: 123,931,819-124,107,666 RILPL1, SNORA9B, 7 more genes
    nsv7074643inversion1nstd229human GRCh38 chr12: 123,471,880-125,706,144 , GRCh37.p13 chr12: 123,956,427-126,190,690 DHX37, RNU6-927P, 44 more genes
    nsv7074199inversion1nstd229human GRCh38 chr12: 123,186,434-132,825,682 , GRCh37.p13 chr12: 123,670,981-133,402,268 PIWIL1, FZD10-AS1, 187 more genes
    nsv7071183inversion1nstd229human GRCh38 chr12: 122,804,561-124,735,813 , GRCh37.p13 chr12: 123,289,108-125,220,359 TMED2, GTF2H3, 41 more genes
    nsv7063627inversion1nstd229human GRCh38 chr12: 123,448,954-124,156,419 , GRCh37.p13 chr12: 123,933,501-124,640,965 ZNF664, CCDC92, 17 more genes
    nsv7060673inversion1nstd229human GRCh38 chr12: 123,243,001-123,542,078 , GRCh37.p13 chr12: 123,727,548-124,026,625 KMT5A, SNRNP35, 11 more genes
    nsv6934866copy number variation1nstd229human GRCh38 chr12: 119,918,701-123,974,100 , GRCh37.p13 chr12: 120,356,505-124,458,647 RNU6-1088P, LOC105370042, 130 more genes
    nsv6934455copy number variation1nstd229human GRCh38 chr12: 123,232,501-123,974,100 , GRCh37.p13 chr12: 123,717,048-124,458,647 MPHOSPH9, MIR8072, 27 more genes
    nsv6931612copy number variation1nstd229human GRCh38 chr12: 123,168,201-123,595,200 , GRCh37.p13 chr12: 123,652,748-124,079,747 SBNO1, MIR3908, 13 more genes
    nsv6925128copy number variation1nstd229human GRCh38 chr12: 123,317,023-123,479,876 , GRCh37.p13 chr12: 123,801,570-123,964,423 RILPL2, SBNO1-AS1, 6 more genes
    nsv6924667copy number variation1nstd229human GRCh38 chr12: 123,455,237-123,461,066 , GRCh37.p13 chr12: 123,939,784-123,945,613 SNRNP35
    nsv6924592copy number variation1nstd229human GRCh38 chr12: 123,377,701-123,457,354 , GRCh37.p13 chr12: 123,862,248-123,941,901 KMT5A, SNRNP35, 2 more genes
    nsv6923985copy number variation1nstd229human GRCh38 chr12: 123,155,001-123,808,300 , GRCh37.p13 chr12: 123,639,548-124,292,847 TMED2-DT, EIF2B1, 24 more genes
    nsv6920363copy number variation1nstd229human GRCh38 chr12: 123,465,641-123,469,248 , GRCh37.p13 chr12: 123,950,188-123,953,795 SNRNP35, RILPL1
    nsv6919987copy number variation1nstd229human GRCh38 chr12: 123,339,501-123,571,300 , GRCh37.p13 chr12: 123,824,048-124,055,847 SBNO1-AS1, RILPL1, 7 more genes
    nsv6588214inversion1nstd223human GRCh38 chr12: 123,468,377-123,469,154 , GRCh37.p13 chr12: 123,952,924-123,953,701 SNRNP35, RILPL1
    nsv6583876inversion1nstd223human GRCh38 chr12: 118,054,469-123,705,974 , GRCh37.p13 chr12: 118,492,274-124,190,521 RPL11P5, RPL17P37, 159 more genes
    nsv6581741inversion1nstd223human GRCh38 chr12: 123,471,879-125,706,143 , GRCh37.p13 chr12: 123,956,426-126,190,689 LOC105370042, TMEM132B, 44 more genes
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