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Items: 1 to 20 of 107

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074641inversion1nstd229human GRCh38 chr12: 52,659,002-59,632,575 , GRCh37.p13 chr12: 53,052,786-60,026,356 , LOC105369777, 292 more genes
    nsv7071931inversion1nstd229human GRCh38 chr12: 55,156,710-64,781,897 , GRCh37.p13 chr12: 55,550,494-65,175,677 ZBTB39, MIR548Z, 236 more genes
    nsv7065167inversion1nstd229human GRCh38 chr12: 55,524,684-56,392,713 , GRCh37.p13 chr12: 55,918,468-56,786,497 TMEM198B, BLOC1S1, 57 more genes
    nsv7060060inversion1nstd229human GRCh38 chr12: 55,500,913-56,344,820 , GRCh37.p13 chr12: 55,894,697-56,738,604 MYL6B, OR6C64P, 54 more genes
    nsv6936083copy number variation1nstd229human GRCh38 chr12: 55,823,301-55,905,900 , GRCh37.p13 chr12: 56,217,085-56,299,684 MMP19, DNAJC14, 5 more genes
    nsv6930717copy number variation1nstd229human GRCh38 chr12: 55,859,450-55,868,960 , GRCh37.p13 chr12: 56,253,234-56,262,744 RN7SL676P, OLA1P3
    nsv6924218copy number variation1nstd229human GRCh38 chr12: 55,714,201-56,819,900 , GRCh37.p13 chr12: 56,107,985-57,213,684 ESYT1, STAT2, 66 more genes
    nsv6637639copy number variation1nstd102humanUncertain significance GRCh37 chr12: 56,056,806-56,438,901 , GRCh38.p12 chr12: 55,663,022-56,045,117 DGKA, PYM1, 24 more genes
    nsv6588914inversion1nstd223human GRCh38 chr12: 55,524,684-56,392,758 , GRCh37.p13 chr12: 55,918,468-56,786,542 IL23A, RPL41, 57 more genes
    nsv6577443inversion1nstd223human GRCh38 chr12: 55,868,559-55,869,203 , GRCh37.p13 chr12: 56,262,343-56,262,987 RN7SL676P, OLA1P3
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv5278526copy number variation1nstd204human GRCh38.p13 chr12: 55,839,801-56,299,500 , GRCh37.p13 chr12: 56,233,585-56,693,284 , NABP2, 30 more genes
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 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
    nsv4675143copy number variation1nstd102humanPathogenic GRCh37 chr12: 55,552,371-62,126,304 , GRCh38.p12 chr12: 55,158,587-61,732,523 OR6C71P, METTL1, 183 more genes
    nsv4342092sequence alteration1nstd166human GRCh37.p13 chr12: 55,894,696-56,786,542 , GRCh38.p12 chr12: 55,500,912-56,392,758 , CD63, 59 more genes
    nsv4324772inversion1nstd166human GRCh37.p13 chr12: 27,368,635-91,765,744 , GRCh38.p12 chr12: 27,215,702-91,371,967 , ATP2B1, 1101 more genes
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