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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075330inversion1nstd229human GRCh38 chr12: 110,682,089-111,481,134 , GRCh37.p13 chr12: 111,119,894-111,918,938 LOC105369981, LINC01405, 15 more genes
    nsv6935035copy number variation1nstd229human GRCh38 chr12: 110,711,283-110,715,937 , GRCh37.p13 chr12: 111,149,088-111,153,742 PPP1CC
    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
    nsv6931541copy number variation1nstd229human GRCh38 chr12: 110,709,801-110,715,900 , GRCh37.p13 chr12: 111,147,606-111,153,705 PPP1CC
    nsv6929334copy number variation1nstd229human GRCh38 chr12: 110,710,101-110,715,700 , GRCh37.p13 chr12: 111,147,906-111,153,505 PPP1CC
    nsv6925406copy number variation1nstd229human GRCh38 chr12: 110,699,970-110,715,912 , GRCh37.p13 chr12: 111,137,775-111,153,717 PPP1CC, HVCN1
    nsv6921217copy number variation1nstd229human GRCh38 chr12: 110,718,797-110,718,896 , GRCh37.p13 chr12: 111,156,602-111,156,701 PPP1CC
    nsv6918907copy number variation1nstd229human GRCh38 chr12: 110,736,663-110,741,271 , GRCh37.p13 chr12: 111,174,468-111,179,076 PPP1CC
    nsv6491519copy number variation1nstd223human GRCh38 chr12: 110,736,663-110,741,283 , GRCh37.p13 chr12: 111,174,468-111,179,088 PPP1CC
    nsv6488418copy number variation1nstd223human GRCh38 chr12: 110,699,901-110,714,900 , GRCh37.p13 chr12: 111,137,706-111,152,705 HVCN1, PPP1CC
    nsv6484997copy number variation1nstd223human GRCh38 chr12: 110,720,868-110,721,099 , GRCh37.p13 chr12: 111,158,673-111,158,904 PPP1CC
    nsv6481878copy number variation1nstd223human GRCh38 chr12: 110,726,501-110,728,400 , GRCh37.p13 chr12: 111,164,306-111,166,205 PPP1CC
    nsv6478639copy number variation1nstd223human GRCh38 chr12: 110,728,429-110,729,006 , GRCh37.p13 chr12: 111,166,234-111,166,811 PPP1CC
    nsv6478139copy number variation1nstd223human GRCh38 chr12: 110,711,281-110,715,934 , GRCh37.p13 chr12: 111,149,086-111,153,739 PPP1CC
    nsv6477712copy number variation1nstd223human GRCh38 chr12: 110,737,619-110,738,773 , GRCh37.p13 chr12: 111,175,424-111,176,578 PPP1CC
    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
    nsv6143329copy number variation1nstd206human GRCh38 chr12: 110,730,617-110,731,767 , GRCh37.p13 chr12: 111,168,422-111,169,572 PPP1CC
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132137copy number variation1nstd213human GRCh37 chr12: 110,580,000-111,480,001 , GRCh38.p12 chr12: 110,142,195-111,042,197 CUX2, IFT81, 21 more genes
    nsv6095645insertion1nstd212human GRCh38 chr12: 110,713,073-110,713,073 , GRCh37.p13 chr12: 111,150,878-111,150,878 PPP1CC
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