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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138731insertion1nstd232human GRCh37.p13 chr12: 133,808,837-133,808,837 , GRCh38.p12 chr12: 133,232,251-133,232,251 ANHX
    nsv7064730inversion1nstd229human GRCh38 chr12: 133,127,727-133,245,552 , GRCh37.p13 chr12: 133,704,313-133,822,138 ANHX, RNU6-717P, 3 more genes
    nsv6936027copy number variation1nstd229human GRCh38 chr12: 133,218,141-133,218,173 , GRCh37.p13 chr12: 133,794,727-133,794,759 ANHX
    nsv6933303copy number variation1nstd229human GRCh38 chr12: 133,177,769-133,225,842 , GRCh37.p13 chr12: 133,754,355-133,802,428 ANHX, ZNF268
    nsv6932814copy number variation1nstd229human GRCh38 chr12: 133,207,671-133,233,811 , GRCh37.p13 chr12: 133,784,257-133,810,397 ANHX, ZNF268
    nsv6928397copy number variation1nstd229human GRCh38 chr12: 133,139,901-133,249,800 , GRCh37.p13 chr12: 133,716,487-133,826,386 ZNF268, ANHX, 2 more genes
    nsv6923966copy number variation1nstd229human GRCh38 chr12: 133,216,804-133,230,619 , GRCh37.p13 chr12: 133,793,390-133,807,205 ANHX
    nsv6923680copy number variation1nstd229human GRCh38 chr12: 133,170,401-133,217,800 , GRCh37.p13 chr12: 133,746,987-133,794,386 ANHX, ZNF268
    nsv6920447copy number variation1nstd229human GRCh38 chr12: 133,202,511-133,216,650 , GRCh37.p13 chr12: 133,779,097-133,793,236 ZNF268, ANHX
    nsv6621525copy number variation1nstd224human GRCh37 chr12: 133,778,796-133,810,935 , GRCh38.p12 chr12: 133,202,210-133,234,349 ANHX, ZNF268
    nsv6487607copy number variation1nstd223human GRCh38 chr12: 133,236,114-133,264,225 , GRCh37.p13 chr12: 133,812,700-133,840,811 ANHX, RNU6-717P
    nsv6481036copy number variation1nstd223human GRCh38 chr12: 133,224,550-133,224,914 , GRCh37.p13 chr12: 133,801,136-133,801,500 ANHX
    nsv6478663copy number variation1nstd223human GRCh38 chr12: 133,202,511-133,216,645 , GRCh37.p13 chr12: 133,779,097-133,793,231 ZNF268, ANHX
    nsv6477694copy number variation1nstd223human GRCh38 chr12: 132,968,857-133,218,887 , GRCh37.p13 chr12: 133,545,443-133,795,473 NANOGNBP2, ZNF84-DT, 10 more genes
    nsv6476120copy number variation1nstd223human GRCh38 chr12: 133,206,285-133,228,463 , GRCh37.p13 chr12: 133,782,871-133,805,049 ZNF268, ANHX
    nsv6290239copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 117,461,902-133,841,395 , GRCh38.p12 chr12: 117,024,097-133,264,809 ACADS, BCL7A, 356 more genes
    nsv6288642insertion1nstd214human GRCh38 chr12: 133,232,281-133,232,281 , GRCh37.p13 chr12: 133,808,867-133,808,867 ANHX
    nsv6288178insertion1nstd214human GRCh38 chr12: 133,232,257-133,232,257 , GRCh37.p13 chr12: 133,808,843-133,808,843 ANHX
    nsv6234429insertion3nstd214human GRCh38 chr12: 133,232,251-133,232,251 , GRCh37.p13 chr12: 133,808,837-133,808,837 ANHX
    nsv6201170copy number variation1nstd214human GRCh38 chr12: 133,235,685-133,235,781 , GRCh37.p13 chr12: 133,812,271-133,812,367 ANHX
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