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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
    nsv7094223copy number variation1nstd102humanUncertain significance GRCh37 chr12: 862,732-2,800,365 , GRCh38.p12 chr12|NW_018654718.1: 1-1,039,315 , GRCh38.p12 chr12: 753,566-2,691,199 DCP1B, CACNA1C-AS2, 28 more genes
    nsv7077070inversion1nstd229human GRCh38 chr12: 1,316,596-1,908,590 , GRCh37.p13 chr12: 1,425,762-2,017,756 LRTM2, LINC00942, 13 more genes
    nsv7075898inversion1nstd229human GRCh38 chr12: 1,484,046-1,626,795 , GRCh37.p13 chr12: 1,593,212-1,735,961 FBXL14, LOC107984507, 3 more genes
    nsv7074168inversion1nstd229human GRCh38 chr12: 1,072,941-1,807,740 , GRCh37.p13 chr12: 1,182,107-1,916,906 LOC105369602, ERC1, 11 more genes
    nsv7067424inversion1nstd229human GRCh38 chr12: 971,399-1,886,809 , GRCh37.p13 chr12: 1,080,565-1,995,975 LRTM2, CACNA2D4, 15 more genes
    nsv7065405inversion1nstd229human GRCh38 chr12: 1,578,737-1,579,156 , GRCh37.p13 chr12: 1,687,903-1,688,322 WNT5B, FBXL14
    nsv7064590inversion1nstd229human GRCh38 chr12: 1,416,708-1,573,914 , GRCh37.p13 chr12: 1,525,874-1,683,080 ERC1, FBXL14, 3 more genes
    nsv7064265inversion1nstd229human GRCh38 chr12: 1,584,860-1,701,989 , GRCh37.p13 chr12: 1,694,026-1,811,155 MIR3649, LOC100533654, 3 more genes
    nsv6915745copy number variation1nstd229human GRCh38 chr12: 1,574,344-1,574,491 , GRCh37.p13 chr12: 1,683,510-1,683,657 FBXL14, WNT5B
    nsv6914465copy number variation1nstd229human GRCh38 chr12: 1,235,301-2,087,900 , GRCh37.p13 chr12: 1,344,467-2,197,066 LINC00940, WNT5B, 18 more genes
    nsv6913361copy number variation1nstd229human GRCh38 chr12: 823,634-1,993,927 , GRCh37.p13 chr12: 932,800-2,103,093 WNT5B, LOC105369601, 19 more genes
    nsv6910273copy number variation1nstd229human GRCh38 chr12: 1,253,201-1,955,300 , GRCh37.p13 chr12: 1,362,367-2,064,466 LOC107987182, LOC105369601, 15 more genes
    nsv6908938copy number variation1nstd229human GRCh38 chr12: 802,301-1,589,216 , GRCh37.p13 chr12: 911,467-1,698,382 WNT5B, WNK1, 7 more genes
    nsv6905145copy number variation1nstd229human GRCh38 chr12: 1,328,481-1,564,235 , GRCh37.p13 chr12: 1,437,647-1,673,401 LINC00942, LOC107984507, 4 more genes
    nsv6904319copy number variation1nstd229human GRCh38 chr12: 1,450,729-1,570,447 , GRCh37.p13 chr12: 1,559,895-1,679,613 LINC00942, LOC107984507, 3 more genes
    nsv6903031copy number variation1nstd229human GRCh38 chr12: 1,484,201-1,592,500 , GRCh37.p13 chr12: 1,593,367-1,701,666 WNT5B, FBXL14, 3 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
    nsv6637310copy number variation1nstd102humanPathogenic GRCh37 chr12: 817,514-2,205,439 , GRCh38.p12 chr12: 708,348-2,096,273 LOC101929432, FBXL14, 24 more genes
    nsv6585425inversion1nstd223human GRCh38 chr12: 1,440,406-2,565,306 , GRCh37.p13 chr12: 1,549,572-2,674,472 LRTM2, LOC107984507, 20 more genes
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