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Items: 1 to 20 of 341

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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
    nsv7094047copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,368,352-9,027,607 , GRCh38.p12 chr12: 4,259,186-8,875,011 ACRBP, OR7E148P, 165 more genes
    nsv7077542inversion1nstd229human GRCh38 chr12: 7,565,102-9,354,075 , GRCh37.p13 chr12: 7,717,698-9,506,671 ALG1L10P, RPL15P17, 69 more genes
    nsv7074628inversion1nstd229human GRCh38 chr12: 5,173,229-8,663,348 , GRCh37.p13 chr12: 5,282,395-8,815,944 P3H3, LOC105369621, 141 more genes
    nsv7074407inversion1nstd229human GRCh38 chr12: 7,895,385-8,483,851 , GRCh37.p13 chr12: 8,047,981-8,636,447 SNRPCP7, NANOGP1, 29 more genes
    nsv7072396inversion1nstd229human GRCh38 chr12: 8,023,307-8,392,436 , GRCh37.p13 chr12: 8,175,903-8,545,032 FAM90A1, POU5F1P3, 18 more genes
    nsv7072221inversion1nstd229human GRCh38 chr12: 4,055,290-11,695,188 , GRCh37.p13 chr12: 4,164,456-11,848,122 RN7SL69P, KLRA1P, 285 more genes
    nsv7068010inversion1nstd229human GRCh38 chr12: 7,025,778-10,225,656 , GRCh37.p13 chr12: 7,178,850-10,378,255 GOT2P3, CLEC2B, 123 more genes
    nsv7064008inversion1nstd229human GRCh38 chr12: 6,716,253-10,225,825 , GRCh37.p13 chr12: 6,825,419-10,378,424 PTMAP4, COPS7A, 153 more genes
    nsv6934553copy number variation1nstd229human GRCh38 chr12: 8,263,269-8,263,494 , GRCh37.p13 chr12: 8,415,865-8,416,090 ENPP7P5, LOC112268090
    nsv6932886copy number variation1nstd229human GRCh38 chr12: 8,258,899-8,288,583 , GRCh37.p13 chr12: 8,411,495-8,441,179 ENPP7P5, LOC112268090
    nsv6931823copy number variation1nstd229human GRCh38 chr12: 8,293,349-8,297,213 , GRCh37.p13 chr12: 8,445,945-8,449,809 LOC112268090
    nsv6927317copy number variation1nstd229human GRCh38 chr12: 8,275,685-8,275,780 , GRCh37.p13 chr12: 8,428,281-8,428,376 LOC112268090
    nsv6925903copy number variation1nstd229human GRCh38 chr12: 8,265,383-8,265,703 , GRCh37.p13 chr12: 8,417,979-8,418,299 ENPP7P5, LOC112268090
    nsv6924164copy number variation1nstd229human GRCh38 chr12: 8,126,744-8,525,670 , GRCh37.p13 chr12: 8,279,340-8,678,266 POU5F1P3, LINC02449, 23 more genes
    nsv6919044copy number variation1nstd229human GRCh38 chr12: 8,293,301-8,297,200 , GRCh37.p13 chr12: 8,445,897-8,449,796 LOC112268090
    nsv6918877copy number variation1nstd229human GRCh38 chr12: 8,250,847-8,250,921 , GRCh37.p13 chr12: 8,403,443-8,403,517 LOC112268090
    nsv6621755copy number variation1nstd224human GRCh37 chr12: 8,376,070-8,509,576 , GRCh38.p12 chr12: 8,223,474-8,356,980 FAM90A1, LINC00937, 7 more genes
    nsv6621754copy number variation1nstd224human GRCh37 chr12: 8,374,746-8,509,669 , GRCh38.p12 chr12: 8,222,150-8,357,073 FAM86FP, SNRPCP7, 9 more genes
    nsv6473973copy number variation1nstd223human GRCh38 chr12: 8,208,701-8,245,000 , GRCh37.p13 chr12: 8,361,297-8,397,596 LINC02449, FAM90A1, 4 more genes
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