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Items: 1 to 20 of 150

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144221copy number variation1nstd232human GRCh37.p13 chr12: 6,639,982-6,640,084 , GRCh38.p12 chr12: 6,530,816-6,530,918 NCAPD2, GAPDH-DT
    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
    nsv7074628inversion1nstd229human GRCh38 chr12: 5,173,229-8,663,348 , GRCh37.p13 chr12: 5,282,395-8,815,944 P3H3, LOC105369621, 141 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
    nsv6935141copy number variation1nstd229human GRCh38 chr12: 6,528,504-6,528,837 , GRCh37.p13 chr12: 6,637,670-6,638,003 NCAPD2, GAPDH-DT
    nsv6929302copy number variation1nstd229human GRCh38 chr12: 6,526,501-6,534,300 , GRCh37.p13 chr12: 6,635,667-6,643,466 GAPDH, NCAPD2, 1 more genes
    nsv6925230copy number variation1nstd229human GRCh38 chr12: 6,418,401-6,902,400 , GRCh37.p13 chr12: 6,527,567-6,907,580 SPSB2, PKP2P1, 36 more genes
    nsv6637376copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,787-8,320,544 , GRCh38.p12 chr12: 64,621-8,167,948 GCSHP4, RNU7-1, 220 more genes
    nsv6621832copy number variation1nstd224human GRCh37 chr12: 6,457,963-6,676,977 , GRCh38.p12 chr12: 6,348,797-6,567,811 LTBR, NOP2, 16 more genes
    nsv6472373copy number variation1nstd223human GRCh38 chr12: 6,012,501-7,083,600 , GRCh37.p13 chr12: 6,121,667-7,189,876 GPR162, CD27, 71 more genes
    nsv6472196copy number variation1nstd223human GRCh38 chr12: 6,013,501-7,083,700 , GRCh37.p13 chr12: 6,122,667-7,189,876 SCARNA10, ATP5MFP5, 71 more genes
    nsv6313934copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,530,146-7,376,398 , GRCh38.p12 chr12: 6,420,980-7,223,802 VAMP1, CD27-AS1, 60 more genes
    nsv6309483copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,438,478-8,756,953 , GRCh38.p12 chr12: 6,329,312-8,604,357 ENPP7P5, GPR162, 122 more genes
    nsv6309326copy number variation2nstd102humanUncertain significance GRCh37 chr12: 6,438,478-8,248,686 , GRCh38.p12 chr12: 6,329,312-8,096,090 NANOGNB, SCNN1A, 94 more genes
    nsv6290254copy number variation1nstd102humanPathogenic GRCh37 chr12: 146,240-8,330,229 , GRCh38.p12 chr12: 45,740-8,177,633 CLEC4A, FBXL14, 220 more genes
    nsv6143107copy number variation1nstd206human GRCh38 chr12: 6,522,000-6,530,000 , GRCh37.p13 chr12: 6,631,166-6,639,166 NCAPD2, GAPDH-DT
    nsv6132704copy number variation1nstd213human GRCh37 chr12: 6,460,000-7,910,001 , GRCh38.p12 chr12: 6,350,834-7,757,405 APOBEC1, C1R, 78 more genes
    nsv6132430copy number variation1nstd213human GRCh37 chr12: 6,290,000-6,680,001 , GRCh38.p12 chr12: 6,180,834-6,570,835 CD9, CHD4, 25 more genes
    nsv6132422copy number variation1nstd213human GRCh37 chr12: 190,000-30,830,001 , GRCh38.p12 chr12: 80,834-30,677,067 , A2M, 622 more genes
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