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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7061495inversion1nstd229human GRCh38 chr12: 107,014,490-109,497,170 , GRCh37.p13 chr12: 107,408,268-109,934,975 RPL17P38, RNU6-361P, 46 more genes
    nsv6936479copy number variation1nstd229human GRCh38 chr12: 109,291,941-109,291,972 , GRCh37.p13 chr12: 109,729,746-109,729,777 FOXN4
    nsv6931732copy number variation1nstd229human GRCh38 chr12: 108,914,683-113,697,537 , GRCh37.p13 chr12: 109,308,459-114,135,342 PTPN11, RPL31P49, 111 more genes
    nsv6931160copy number variation1nstd229human GRCh38 chr12: 109,150,901-109,317,900 , GRCh37.p13 chr12: 109,588,706-109,755,705 FOXN4, ACACB
    nsv6929200copy number variation1nstd229human GRCh38 chr12: 109,289,974-109,290,156 , GRCh37.p13 chr12: 109,727,779-109,727,961 FOXN4
    nsv6927918copy number variation1nstd229human GRCh38 chr12: 109,309,396-109,309,916 , GRCh37.p13 chr12: 109,747,201-109,747,721 FOXN4
    nsv6924350copy number variation1nstd229human GRCh38 chr12: 109,293,301-109,319,600 , GRCh37.p13 chr12: 109,731,106-109,757,405 FOXN4
    nsv6922947copy number variation1nstd229human GRCh38 chr12: 108,490,015-109,627,369 , GRCh37.p13 chr12: 108,883,792-110,065,174 RNU4-32P, LOC105369968, 30 more genes
    nsv6621489copy number variation1nstd224human GRCh37 chr12: 109,201,326-110,355,704 , GRCh38.p12 chr12: 108,807,550-109,917,899 FAM222A, MYO1H, 29 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
    nsv6203732copy number variation1nstd214human GRCh38 chr12: 109,284,824-109,284,954 , GRCh37.p13 chr12: 109,722,629-109,722,759 FOXN4
    nsv6191735copy number variation1nstd214human GRCh38 chr12: 109,284,846-109,284,976 , GRCh37.p13 chr12: 109,722,651-109,722,781 FOXN4
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132406copy number variation1nstd213human GRCh37 chr12: 108,420,000-110,500,001 , GRCh38.p12 chr12: 108,026,223-110,062,196 DAO, SART3, 47 more genes
    nsv6099716insertion1nstd212human GRCh38 chr12: 109,304,254-109,304,254 , GRCh37.p13 chr12: 109,742,059-109,742,059 FOXN4
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv4995535copy number variation1nstd200human GRCh38 chr12: 109,287,919-109,288,883 , GRCh37.p13 chr12: 109,725,724-109,726,688 FOXN4
    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
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