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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7059124inversion1nstd229human GRCh38 chr12: 109,811,295-109,871,385 , GRCh37.p13 chr12: 110,249,100-110,309,190 GLTP, TRPV4, 3 more genes
    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
    nsv6930109copy number variation1nstd229human GRCh38 chr12: 109,794,479-109,885,553 , GRCh37.p13 chr12: 110,232,284-110,323,358 GLTP, TRPV4, 4 more genes
    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
    nsv6924909copy number variation1nstd229human GRCh38 chr12: 109,793,168-109,795,498 , GRCh37.p13 chr12: 110,230,973-110,233,303 TRPV4
    nsv6923215copy number variation1nstd229human GRCh38 chr12: 109,785,927-109,791,989 , GRCh37.p13 chr12: 110,223,732-110,229,794 TRPV4
    nsv6920405copy number variation1nstd229human GRCh38 chr12: 109,808,762-109,808,821 , GRCh37.p13 chr12: 110,246,567-110,246,626 TRPV4
    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
    nsv6589578inversion1nstd223human GRCh38 chr12: 109,825,061-109,825,221 , GRCh37.p13 chr12: 110,262,866-110,263,026 TRPV4
    nsv6490507copy number variation1nstd223human GRCh38 chr12: 109,820,701-109,824,200 , GRCh37.p13 chr12: 110,258,506-110,262,005 TRPV4
    nsv6476107copy number variation1nstd223human GRCh38 chr12: 109,794,479-109,885,546 , GRCh37.p13 chr12: 110,232,284-110,323,351 GLTP, TRPV4, 4 more genes
    nsv6309461copy number variation1nstd102humanUncertain significance GRCh37 chr12: 110,252,196-110,252,601 , GRCh38.p12 chr12: 109,814,391-109,814,796 TRPV4
    nsv6309397copy number variation1nstd102humanUncertain significance GRCh37 chr12: 110,221,426-110,224,662 , GRCh38.p12 chr12: 109,783,621-109,786,857 TRPV4
    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
    nsv6272379copy number variation1nstd214human GRCh38 chr12: 109,808,841-109,809,005 , GRCh37.p13 chr12: 110,246,646-110,246,810 TRPV4
    nsv6270538copy number variation1nstd214human GRCh38 chr12: 109,827,802-109,827,853 , GRCh37.p13 chr12: 110,265,607-110,265,658 TRPV4
    nsv6197131copy number variation1nstd214human GRCh38 chr12: 109,808,986-109,809,040 , GRCh37.p13 chr12: 110,246,791-110,246,845 TRPV4
    nsv6192181copy number variation1nstd214human GRCh38 chr12: 109,808,762-109,808,820 , GRCh37.p13 chr12: 110,246,567-110,246,625 TRPV4
    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
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