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Items: 1 to 20 of 310

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068942inversion1nstd229human GRCh38 chr12: 109,744,360-109,746,438 , GRCh37.p13 chr12: 110,182,165-110,184,243 FAM222A-AS1, FAM222A
    nsv6936608copy number variation1nstd229human GRCh38 chr12: 109,770,951-109,772,637 , GRCh37.p13 chr12: 110,208,756-110,210,442 FAM222A-AS1, FAM222A
    nsv6936373copy number variation1nstd229human GRCh38 chr12: 109,717,683-109,717,802 , GRCh37.p13 chr12: 110,155,488-110,155,607 FAM222A
    nsv6933544copy number variation1nstd229human GRCh38 chr12: 109,760,026-109,760,101 , GRCh37.p13 chr12: 110,197,831-110,197,906 FAM222A-AS1, FAM222A
    nsv6932941copy number variation1nstd229human GRCh38 chr12: 109,753,734-109,757,480 , GRCh37.p13 chr12: 110,191,539-110,195,285 FAM222A-AS1, FAM222A
    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
    nsv6931675copy number variation1nstd229human GRCh38 chr12: 109,729,001-109,731,247 , GRCh37.p13 chr12: 110,166,806-110,169,052 FAM222A
    nsv6931301copy number variation1nstd229human GRCh38 chr12: 109,737,410-109,737,452 , GRCh37.p13 chr12: 110,175,215-110,175,257 FAM222A, FAM222A-AS1
    nsv6928731copy number variation1nstd229human GRCh38 chr12: 109,701,301-109,906,300 , GRCh37.p13 chr12: 110,139,106-110,344,105 TRPV4, RN7SL441P, 6 more genes
    nsv6927407copy number variation1nstd229human GRCh38 chr12: 109,756,689-109,764,132 , GRCh37.p13 chr12: 110,194,494-110,201,937 FAM222A, FAM222A-AS1
    nsv6926155copy number variation1nstd229human GRCh38 chr12: 109,713,614-109,719,294 , GRCh37.p13 chr12: 110,151,419-110,157,099 FAM222A
    nsv6925673copy number variation1nstd229human GRCh38 chr12: 109,720,872-109,735,565 , GRCh37.p13 chr12: 110,158,677-110,173,370 FAM222A, FAM222A-AS1
    nsv6919597copy number variation1nstd229human GRCh38 chr12: 109,763,052-109,765,915 , GRCh37.p13 chr12: 110,200,857-110,203,720 FAM222A, FAM222A-AS1
    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
    nsv6493894copy number variation1nstd223human GRCh38 chr12: 109,770,951-109,772,637 , GRCh37.p13 chr12: 110,208,756-110,210,442 FAM222A, FAM222A-AS1
    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
    nsv6285797insertion1nstd214human GRCh38 chr12: 109,760,026-109,760,026 , GRCh37.p13 chr12: 110,197,831-110,197,831 FAM222A, FAM222A-AS1
    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
    nsv6087460insertion1nstd212human GRCh38 chr12: 109,738,795-109,738,795 , GRCh37.p13 chr12: 110,176,600-110,176,600 FAM222A, FAM222A-AS1
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