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Items: 1 to 20 of 136

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5867383copy number variation2nstd209human GRCh38 chr12: 122,709,216-122,712,932 , GRCh37.p13 chr12: 123,193,763-123,197,479 MIR9902-2, HCAR3
    nsv5867298copy number variation2nstd209human GRCh38 chr12: 122,715,546-122,716,939 , GRCh37.p13 chr12: 123,200,093-123,201,486 HCAR3
    nsv5866424copy number variation2nstd209human GRCh38 chr12: 122,706,455-122,715,745 , GRCh37.p13 chr12: 123,191,002-123,200,292 MIR9902-2, HCAR3
    nsv5865706copy number variation1nstd209human GRCh38 chr12: 122,708,858-122,715,082 , GRCh37.p13 chr12: 123,193,405-123,199,629 HCAR3, MIR9902-2
    nsv5863108copy number variation1nstd209human GRCh38 chr12: 122,708,857-122,715,745 , GRCh37.p13 chr12: 123,193,404-123,200,292 HCAR3, MIR9902-2
    nsv5857203copy number variation2nstd209human GRCh38 chr12: 122,700,851-122,716,221 , GRCh37.p13 chr12: 123,185,398-123,200,768 HCAR2, MIR9902-2, 1 more genes
    nsv5512317copy number variation1nstd206human GRCh38 chr12: 122,702,594-122,716,849 , GRCh37.p13 chr12: 123,187,141-123,201,396 HCAR2, MIR9902-2, 1 more genes
    nsv5279919copy number variation1nstd204human GRCh38.p13 chr12: 122,712,091-122,714,982 , GRCh37.p13 chr12: 123,196,638-123,199,529 HCAR3
    nsv5270943copy number variation1nstd204human GRCh38.p13 chr12: 122,704,301-122,717,700 , GRCh37.p13 chr12: 123,188,848-123,202,247 HCAR3, MIR9902-2
    nsv5267981copy number variation1nstd204human GRCh38.p13 chr12: 122,705,145-122,719,045 , GRCh37.p13 chr12: 123,189,692-123,203,592 MIR9902-2, HCAR3
    nsv5266919copy number variation1nstd204human GRCh38.p13 chr12: 122,717,101-122,721,100 , GRCh37.p13 chr12: 123,201,648-123,205,647 HCAR3
    nsv5265878copy number variation1nstd204human GRCh38.p13 chr12: 122,712,687-122,715,645 , GRCh37.p13 chr12: 123,197,234-123,200,192 HCAR3
    nsv4996126copy number variation1nstd200human GRCh38 chr12: 122,704,836-122,718,378 , GRCh37.p13 chr12: 123,189,383-123,202,925 HCAR3, MIR9902-2
    nsv4993810copy number variation1nstd200human GRCh38 chr12: 122,705,414-122,719,383 , GRCh37.p13 chr12: 123,189,961-123,203,930 MIR9902-2, HCAR3
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4754840inversion1nstd199human GRCh37 chr12: 104,382,539-125,801,164 , GRCh38.p12 chr12: 103,988,761-125,316,618 , ACACB, 452 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4672362copy number variation1nstd186human GRCh37 chr12: 123,185,580-123,198,603 , GRCh38.p12 chr12: 122,701,033-122,714,056 HCAR3, HCAR2, 1 more genes
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