U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 4572

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4336854sequence alteration1nstd166human GRCh37.p13 chr3: 78,251,415-78,581,622 , GRCh38.p12 chr3: 78,202,264-78,532,472 MRPS17P3
    nsv4338115sequence alteration1nstd166human GRCh37.p13 chr18: 64,238,641-64,556,936 , GRCh38.p12 chr18: 66,571,404-66,889,699 CDH19
    nsv4342170sequence alteration1nstd166human GRCh37.p13 chr7: 12,975,647-13,293,577 , GRCh38.p12 chr7: 12,936,022-13,253,952 LOC105375158
    nsv4343963sequence alteration1nstd166human GRCh37.p13 chr3: 4,141,767-4,334,804 , GRCh38.p12 chr3: 4,100,083-4,293,120 SUMF1
    nsv4336894sequence alteration1nstd166human GRCh37.p13 chr12: 61,456,584-61,645,395 , GRCh38.p12 chr12: 61,062,803-61,251,614 PGBD3P1
    nsv4335766sequence alteration1nstd166human GRCh37.p13 chr4: 134,921,833-135,108,666 , GRCh38.p12 chr4: 134,000,678-134,187,511 PABPC4L
    nsv4573105sequence alteration1nstd166human GRCh37.p13 chr6: 1,913,470-2,085,419 , GRCh38.p12 chr6: 1,913,236-2,085,185 GMDS
    nsv4337055sequence alteration1nstd166human GRCh37.p13 chr3: 154,688,810-154,858,341 , GRCh38.p12 chr3: 154,971,021-155,140,552 MME
    nsv4563015sequence alteration1nstd166human GRCh37.p13 chrX: 19,210,735-19,369,467 , GRCh38.p12 chrX: 19,192,617-19,351,349 PDHA1
    nsv4336559sequence alteration1nstd166human GRCh37.p13 chr13: 64,579,930-64,737,523 , GRCh38.p12 chr13: 64,005,797-64,163,391 LINC00355
    nsv4570438sequence alteration1nstd166human GRCh37.p13 chr7: 57,719,035-57,875,191 , GRCh38.p12 chr7: 57,659,329-57,815,485 LOC105375302
    nsv4339288sequence alteration1nstd166human GRCh37.p13 chr2: 123,778,634-123,933,974 , GRCh38.p12 chr2: 123,021,058-123,176,398 LINC01826
    nsv4332896sequence alteration1nstd166human GRCh37.p13 chr14: 42,969,498-43,119,280 , GRCh38.p12 chr14: 42,500,295-42,650,077 LOC100420765
    nsv4324643sequence alteration1nstd166human GRCh37.p13 chrX: 57,761,420-57,909,099 , GRCh38.p12 chrX: 57,734,987-57,882,665 MDH1P1
    nsv4557703sequence alteration1nstd166human GRCh37.p13 chr9: 20,164,480-20,310,776 , GRCh38.p12 chr9: 20,164,482-20,310,778 SLC24A2
    nsv4341842sequence alteration1nstd166human GRCh37.p13 chr3: 7,954,052-8,097,772 , GRCh38.p12 chr3: 7,912,365-8,056,085 LOC101927394
    nsv4338656sequence alteration1nstd166human GRCh37.p13 chr7: 119,389,202-119,520,754 , GRCh38.p12 chr7: 119,749,148-119,880,700 LINC02476
    nsv4333377sequence alteration1nstd166human GRCh37.p13 chr2: 188,902,947-189,034,333 , GRCh38.p12 chr2: 188,038,220-188,169,606 LINC01090
    nsv4334631sequence alteration1nstd166human GRCh37.p13 chr7: 18,387,687-18,514,349 , GRCh38.p12 chr7: 18,348,064-18,474,726 HDAC9
    nsv4333897sequence alteration1nstd166human GRCh37.p13 chr4: 19,275,192-19,399,859 , GRCh38.p12 chr4: 19,273,569-19,398,236 LINC02438
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center