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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7067004inversion1nstd229human GRCh38 chr12: 106,853,473-107,177,792 , GRCh37.p13 chr12: 107,247,251-107,571,570 CRY1, TMEM263, 5 more genes
    nsv6931869copy number variation1nstd229human GRCh38 chr12: 106,968,748-106,975,711 , GRCh37.p13 chr12: 107,362,526-107,369,489 MTERF2, TMEM263
    nsv6919997copy number variation1nstd229human GRCh38 chr12: 106,974,401-106,982,200 , GRCh37.p13 chr12: 107,368,179-107,375,978 TMEM263, MTERF2
    nsv6621055copy number variation1nstd224human GRCh37 chr12: 107,360,920-107,630,497 , GRCh38.p12 chr12: 106,967,142-107,236,719 CRY1, MTERF2, 1 more genes
    nsv6291583copy number variation1nstd102humanPathogenic GRCh37 chr12: 104,230,462-111,984,801 , GRCh38.p12 chr12: 103,836,684-111,546,997 LOC105369964, LOC644746, 147 more genes
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132319copy number variation1nstd213human GRCh37 chr12: 106,860,000-107,430,001 , GRCh38.p12 chr12: 106,466,222-107,036,223 LOC105369961, POLR3B, 9 more genes
    nsv5945330copy number variation1nstd209human GRCh38 chr12: 106,954,096-106,954,145 , GRCh37.p13 chr12: 107,347,874-107,347,923 TMEM263
    nsv5713096mobile element insertion1nstd211human GRCh38 chr12: 106,964,978-106,964,978 , GRCh37.p13 chr12: 107,358,756-107,358,756 TMEM263
    nsv5424059mobile element insertion1nstd206human GRCh38 chr12: 106,964,978-106,965,029 , GRCh37.p13 chr12: 107,358,756-107,358,807 TMEM263
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    nsv4769383copy number variation1nstd102humanUncertain significance GRCh37 chr12: 107,197,584-109,830,564 , GRCh38.p12 chr12: 106,803,806-109,392,759 TMEM263, MYO1H, 50 more genes
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4754840inversion1nstd199human GRCh37 chr12: 104,382,539-125,801,164 , GRCh38.p12 chr12: 103,988,761-125,316,618 , ACACB, 452 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
    nsv4728881copy number variation1nstd102humanPathogenic GRCh37 chr12: 106,498,814-112,252,906 , GRCh38.p12 chr12: 106,105,036-111,815,102 ATP2A2, CUX2, 115 more genes
    nsv4505478mobile element insertion1nstd166human GRCh37.p13 chr12: 107,358,741-107,358,741 , GRCh38.p12 chr12: 106,964,963-106,964,963 TMEM263
    nsv4498841mobile element insertion1nstd166human GRCh37.p13 chr12: 107,363,066-107,363,066 , GRCh38.p12 chr12: 106,969,288-106,969,288 TMEM263
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