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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
    nsv7093966copy number variation1nstd102humanUncertain significance GRCh37 chr12: 20,522,219-22,089,608 , GRCh38.p12 chr12: 20,369,285-21,936,674 LOC728688, SPX, 19 more genes
    nsv7076490inversion1nstd229human GRCh38 chr12: 20,940,376-25,948,754 , GRCh37.p13 chr12: 21,093,310-26,101,687 LOC102724261, IRAG2, 59 more genes
    nsv7072461inversion1nstd229human GRCh38 chr12: 21,060,700-21,582,859 , GRCh37.p13 chr12: 21,213,634-21,735,793 RECQL, SLCO1B1, 9 more genes
    nsv7072309inversion1nstd229human GRCh38 chr12: 20,907,972-21,582,861 , GRCh37.p13 chr12: 21,060,906-21,735,795 RECQL, SLCO1B1, 10 more genes
    nsv7070485inversion1nstd229human GRCh38 chr12: 21,009,516-22,041,867 , GRCh37.p13 chr12: 21,162,450-22,194,801 SLCO1B3-SLCO1B7, SPX, 15 more genes
    nsv7070248inversion1nstd229human GRCh38 chr12: 21,603,481-21,607,288 , GRCh37.p13 chr12: 21,756,415-21,760,222 GYS2
    nsv7068678inversion1nstd229human GRCh38 chr12: 20,996,324-22,051,286 , GRCh37.p13 chr12: 21,149,258-22,204,220 SLCO1B3-SLCO1B7, ABCC9, 16 more genes
    nsv7068185inversion1nstd229human GRCh38 chr12: 20,036,076-21,999,484 , GRCh37.p13 chr12: 20,189,010-22,152,418 UBE2L2, RECQL, 25 more genes
    nsv7063671inversion1nstd229human GRCh38 chr12: 20,030,237-21,994,711 , GRCh37.p13 chr12: 20,183,171-22,147,645 SLCO1B3-SLCO1B7, LINC02468, 25 more genes
    nsv7060644inversion1nstd229human GRCh38 chr12: 20,030,249-21,999,483 , GRCh37.p13 chr12: 20,183,183-22,152,417 SLCO1B3-SLCO1B7, SLCO1B3, 25 more genes
    nsv7058207inversion1nstd229human GRCh38 chr12: 21,601,414-21,601,471 , GRCh37.p13 chr12: 21,754,348-21,754,405 GYS2
    nsv6936345copy number variation1nstd229human GRCh38 chr12: 21,532,863-21,620,238 , GRCh37.p13 chr12: 21,685,797-21,773,172 SPX, GYS2
    nsv6929125copy number variation1nstd229human GRCh38 chr12: 21,584,373-21,584,408 , GRCh37.p13 chr12: 21,737,307-21,737,342 GYS2
    nsv6924577copy number variation1nstd229human GRCh38 chr12: 21,248,929-21,619,602 , GRCh37.p13 chr12: 21,401,863-21,772,536 GYS2, GOLT1B, 6 more genes
    nsv6924555copy number variation1nstd229human GRCh38 chr12: 21,568,384-21,572,961 , GRCh37.p13 chr12: 21,721,318-21,725,895 GYS2
    nsv6924018copy number variation1nstd229human GRCh38 chr12: 21,553,695-21,602,545 , GRCh37.p13 chr12: 21,706,629-21,755,479 GYS2
    nsv6921691copy number variation1nstd229human GRCh38 chr12: 21,518,083-21,588,617 , GRCh37.p13 chr12: 21,671,017-21,741,551 GOLT1B, SPX, 1 more genes
    nsv6634456copy number variation1nstd102humanPathogenic GRCh37 chr12: 10,853,887-24,103,810 , GRCh38.p12 chr12: 10,701,288-23,950,876 TAS2R15P, LOC105369673, 209 more genes
    nsv6590282inversion1nstd223human GRCh38 chr12: 20,907,972-21,582,861 , GRCh37.p13 chr12: 21,060,906-21,735,795 IAPP, GOLT1B, 10 more genes
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