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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5973645copy number variation1nstd209human GRCh38 chrX: 1,391,092-1,400,080 , GRCh37.p13 chrX: 1,509,985-1,518,973 , SLC25A6, 2 more genes
    nsv5968396copy number variation1nstd209human GRCh38 chrX: 1,384,568-1,390,366 , GRCh37.p13 chrX: 1,503,461-1,509,259 , SLC25A6
    nsv5869082copy number variation1nstd209human GRCh38 chrX: 1,388,413-1,388,631 , GRCh37.p13 chrX: 1,507,306-1,507,524 SLC25A6
    nsv5671782inversion1nstd207human GRCh38 chrY: 10,002-57,217,414 , GRCh37.p13 chrY: 10,002-59,363,565 , ACTG1P2, 580 more genes
    nsv5605772insertion1nstd207human GRCh38 chrX: 1,390,754-1,390,754 , GRCh37.p13 chrX: 1,509,647-1,509,647 , SLC25A6
    nsv5604716insertion1nstd207human GRCh38 chrY: 1,390,754-1,390,754 , GRCh37.p13 chrY: 1,459,647-1,459,647 , SLC25A6
    nsv5564472copy number variation1nstd102humanPathogenic GRCh37 chrY: 10,701-5,080,415 , GRCh38.p12 chrY: 10,701-5,212,374 AGPAT5P1, NAP1L1P2, 58 more genes
    nsv5556906sequence alteration1nstd206human GRCh38 chrX: 1,348,093-1,930,225 , GRCh37.p13 chrX: 1,466,986-2,049,118 , ASMTL-AS1, 14 more genes
    nsv5432327copy number variation1nstd206human GRCh38 chrX: 10,000-2,781,000 , GRCh37.p13 chrX: 60,001-2,699,041 , IL3RA, 40 more genes
    nsv5418515copy number variation1nstd206human GRCh38 chrX: 864,608-1,428,971 , GRCh37.p13 chrX: 932,710-1,547,864 , SLC25A6, 15 more genes
    nsv5366322translocation1nstd200human GRCh38 chrX: 1,391,897-1,391,897 , GRCh38 chrX: 1,390,294-1,390,294 , GRCh37.p13 chrX: 1,509,187-1,509,187 , GRCh37.p13 chrX: 1,510,790-1,510,790 , SLC25A6
    nsv5366321translocation1nstd200human GRCh38 chrX: 1,391,896-1,391,896 , GRCh38 chrX: 1,389,730-1,389,730 , GRCh37.p13 chrX: 1,508,623-1,508,623 , GRCh37.p13 chrX: 1,510,789-1,510,789 , SLC25A6
    nsv5366320translocation1nstd200human GRCh38 chrX: 1,389,239-1,389,239 , GRCh38 chrX: 1,387,420-1,387,420 , GRCh37.p13 chrX: 1,508,132-1,508,132 , GRCh37.p13 chrX: 1,506,313-1,506,313 SLC25A6
    nsv5357558translocation1nstd200human GRCh38 chr14: 93,312,377-93,312,377 , GRCh38 chrX: 1,392,111-1,392,111 , GRCh37.p13 chr14: 93,778,723-93,778,723 , GRCh37.p13 chrX: 1,511,004-1,511,004 , SLC25A6, 1 more genes
    nsv5332017translocation1nstd200human GRCh37 chrX: 1,503,450-1,503,450 , GRCh37 chrX: 1,503,976-1,503,976 , GRCh38.p12 chrX: 1,384,557-1,384,557 , GRCh38.p12 chrX: 1,385,083-1,385,083 SLC25A6
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv4905060copy number variation1nstd200human GRCh38 chrX: 1,210,273-1,496,953 , GRCh37.p13 chrX: 1,329,166-1,615,846 , LINC00106, 13 more genes
    nsv4905055copy number variation1nstd200human GRCh38 chrX: 1,162,318-1,452,888 , GRCh37.p13 chrX: 1,262,471-1,571,781 , MIR3690, 13 more genes
    nsv4905048copy number variation1nstd200human GRCh38 chrX: 1,066,190-1,385,635 , GRCh37.p13 chrX: 1,227,823-1,504,528 , LOC652608, 10 more genes
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