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Items: 1 to 20 of 278

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7139421insertion1nstd232human GRCh37.p13 chr15: 89,858,743-89,858,743 , GRCh38.p12 chr15: 89,315,512-89,315,512 POLG, FANCI
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7098892copy number variation1nstd102humanPathogenic GRCh37 chr15: 84,228,005-102,264,590 , GRCh38.p12 chr15: 83,559,253-101,724,387 CIB1, RPS12P26, 326 more genes
    nsv7094742copy number variation1nstd102humanPathogenic GRCh37 chr15: 89,862,161-89,864,158 , GRCh38.p12 chr15: 89,318,930-89,320,927 POLG
    nsv7094314copy number variation1nstd102humanUncertain significance GRCh37 chr15: 89,859,982-89,876,985 , GRCh38.p12 chr15: 89,316,751-89,333,754 MIR6766, TRR-TCG1-1, 2 more genes
    nsv7094312copy number variation2nstd102humanUncertain significance GRCh37 chr15: 89,379,429-91,565,479 , GRCh38.p12 chr15: 88,836,198-91,022,249 IQGAP1, WDR93, 77 more genes
    nsv7093075copy number variation1nstd102humanPathogenic GRCh37 chr15: 89,876,329-89,876,434 , GRCh38 chr15: 89,333,098-89,333,203 TRR-TCG1-1, POLG
    nsv7076849inversion1nstd229human GRCh38 chr15: 89,041,443-89,639,935 , GRCh37.p13 chr15: 89,584,674-90,183,166 LINC00928, HMGB1P8, 17 more genes
    nsv7068128inversion1nstd229human GRCh38 chr15: 87,287,023-90,484,635 , GRCh37.p13 chr15: 87,830,254-91,027,867 , LOC105370964, 81 more genes
    nsv7065612inversion1nstd229human GRCh38 chr15: 89,041,442-91,616,740 , GRCh37.p13 chr15: 89,584,673-92,159,970 ZNF774, CRAT37, 77 more genes
    nsv7062993inversion1nstd229human GRCh38 chr15: 85,570,479-90,463,746 , GRCh37.p13 chr15: 86,113,710-91,006,978 , NTRK3-AS1, 97 more genes
    nsv6976816copy number variation1nstd229human GRCh38 chr15: 89,315,512-89,315,592 , GRCh37.p13 chr15: 89,858,743-89,858,823 POLG, FANCI
    nsv6976510copy number variation1nstd229human GRCh38 chr15: 86,730,503-91,149,191 , GRCh37.p13 chr15: 87,273,734-91,692,421 , IQGAP1, 105 more genes
    nsv6976325copy number variation1nstd229human GRCh38 chr15: 89,324,123-89,332,364 , GRCh37.p13 chr15: 89,867,354-89,875,595 MIR6766, POLG
    nsv6970586copy number variation1nstd229human GRCh38 chr15: 89,318,931-89,320,930 , GRCh37.p13 chr15: 89,862,162-89,864,161 POLG
    nsv6962279copy number variation1nstd229human GRCh38 chr15: 89,323,099-89,323,607 , GRCh37.p13 chr15: 89,866,330-89,866,838 POLG
    nsv6637683copy number variation1nstd102humanPathogenic GRCh37 chr15: 77,512,817-102,035,027 , GRCh38.p12 chr15: 77,220,475-101,494,824 LINC02253, LOC107984790, 463 more genes
    nsv6634636copy number variation1nstd102humanBenign GRCh38 chr15: 89,325,035-89,325,232 , GRCh37 chr15: 89,868,266-89,868,463 MIR6766, POLG
    nsv6634603copy number variation1nstd102humanBenign GRCh37 chr15: 89,868,285-89,868,486 , GRCh38 chr15: 89,325,054-89,325,255 MIR6766, POLG
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