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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
    nsv7076234inversion1nstd229human GRCh38 chr12: 110,868,174-112,310,507 , GRCh37.p13 chr12: 111,305,978-112,748,311 LOC105369983, RN7SKP71, 35 more genes
    nsv7075330inversion1nstd229human GRCh38 chr12: 110,682,089-111,481,134 , GRCh37.p13 chr12: 111,119,894-111,918,938 LOC105369981, LINC01405, 15 more genes
    nsv7061496inversion1nstd229human GRCh38 chr12: 110,868,674-111,441,001 , GRCh37.p13 chr12: 111,306,478-111,878,805 LOC105369981, LINC01405, 11 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
    nsv6927187copy number variation1nstd229human GRCh38 chr12: 111,422,707-111,429,479 , GRCh37.p13 chr12: 111,860,511-111,867,283 SH2B3
    nsv6926975copy number variation1nstd229human GRCh38 chr12: 111,425,305-111,425,886 , GRCh37.p13 chr12: 111,863,109-111,863,690 SH2B3
    nsv6921934copy number variation1nstd229human GRCh38 chr12: 111,439,568-111,439,942 , GRCh37.p13 chr12: 111,877,372-111,877,746 SH2B3
    nsv6921140copy number variation1nstd229human GRCh38 chr12: 111,424,401-111,426,900 , GRCh37.p13 chr12: 111,862,205-111,864,704 SH2B3
    nsv6918394copy number variation1nstd229human GRCh38 chr12: 111,433,877-111,439,413 , GRCh37.p13 chr12: 111,871,681-111,877,217 SH2B3
    nsv6475929copy number variation1nstd223human GRCh38 chr12: 111,422,706-111,429,398 , GRCh37.p13 chr12: 111,860,510-111,867,202 SH2B3
    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
    nsv6132407copy number variation1nstd213human GRCh37 chr12: 111,690,000-112,220,001 , GRCh38.p12 chr12: 111,252,196-111,782,197 ATXN2, SH2B3, 13 more genes
    nsv6132202copy number variation1nstd213human GRCh37 chr12: 111,609,061-111,887,989 , GRCh38.p12 chr12: 111,171,257-111,450,185 SH2B3, CUX2, 6 more genes
    nsv6132129copy number variation1nstd213human GRCh37 chr12: 111,609,491-111,887,986 , GRCh38.p12 chr12: 111,171,687-111,450,182 SH2B3, CUX2, 6 more genes
    nsv6029944copy number variation1nstd212human GRCh38 chr12: 111,420,222-111,420,322 , GRCh37.p13 chr12: 111,858,026-111,858,126 SH2B3
    nsv5928982copy number variation1nstd209human GRCh38 chr12: 111,422,669-111,429,435 , GRCh37.p13 chr12: 111,860,473-111,867,239 SH2B3
    nsv5864396copy number variation2nstd209human GRCh38 chr12: 111,426,906-111,428,005 , GRCh37.p13 chr12: 111,864,710-111,865,809 SH2B3
    nsv5862785copy number variation1nstd209human GRCh38 chr12: 111,425,206-111,429,560 , GRCh37.p13 chr12: 111,863,010-111,867,364 SH2B3
    nsv5860252copy number variation2nstd209human GRCh38 chr12: 111,423,306-111,424,305 , GRCh37.p13 chr12: 111,861,110-111,862,109 SH2B3
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