U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 132

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048284inversion1nstd229human GRCh38 chr6: 73,272,579-75,940,581 , GRCh37.p13 chr6: 73,982,302-76,650,298 RPL39P3, KHDC1, 45 more genes
    nsv7043838inversion1nstd229human GRCh38 chr6: 73,208,570-73,391,551 , GRCh37.p13 chr6: 73,918,293-74,101,274 RPSAP41, KHDC3L, 10 more genes
    nsv6790487copy number variation1nstd229human GRCh38 chr6: 73,006,301-73,863,300 , GRCh37.p13 chr6: 73,716,024-74,573,015 RBPMS2P1, SLC17A5, 24 more genes
    nsv6787789copy number variation1nstd229human GRCh38 chr6: 73,224,501-73,533,000 , GRCh37.p13 chr6: 73,934,224-74,242,723 DDX43, KHDC3L, 15 more genes
    nsv6787581copy number variation1nstd229human GRCh38 chr6: 73,352,980-73,353,144 , GRCh37.p13 chr6: 74,062,703-74,062,867 DPPA5
    nsv6784485copy number variation1nstd229human GRCh38 chr6: 73,256,414-73,487,243 , GRCh37.p13 chr6: 73,966,137-74,196,966 OOEP, RN7SL827P, 13 more genes
    nsv6634377copy number variation1nstd102humanPathogenic GRCh37 chr6: 71,105,038-75,200,617 , GRCh38.p12 chr6: 70,395,335-74,490,901 TXNP7, MTO1, 63 more genes
    nsv6573990inversion1nstd223human GRCh38 chr6: 73,118,474-73,446,748 , GRCh37.p13 chr6: 73,828,197-74,156,471 DPPA5, EIF3EP1, 15 more genes
    nsv6559734inversion1nstd223human GRCh38 chr6: 66,921,420-73,446,758 , GRCh37.p13 chr6: 67,631,313-74,156,481 RNA5SP208, KCNQ5, 72 more genes
    nsv6402883copy number variation1nstd223human GRCh38 chr6: 73,324,000-73,364,974 , GRCh37.p13 chr6: 74,033,723-74,074,697 KHDC3L, PAICSP3, 1 more genes
    nsv6315402copy number variation1nstd102humanPathogenic GRCh37 chr6: 64,954,687-79,581,678 , GRCh38.p12 chr6: 64,244,794-78,871,961 LOC105377841, RPS6P8, 139 more genes
    nsv6313857copy number variation1nstd102humanPathogenic GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492 LOC101928570, RNU4-72P, 288 more genes
    nsv6312591copy number variation1nstd102humanUncertain significance GRCh37 chr6: 73,879,449-74,210,458 , GRCh38.p12 chr6: 73,169,726-73,500,735 KCNQ5, DPPA5, 16 more genes
    nsv6291339copy number variation1nstd102humanPathogenic GRCh37 chr6: 70,165,296-79,920,769 , GRCh38.p12 chr6: 69,455,404-79,211,052 RNU6-84P, PGAM1P10, 113 more genes
    nsv6291322copy number variation1nstd102humanPathogenic GRCh37 chr6: 72,799,054-83,275,894 , GRCh38.p12 chr6: 72,089,351-82,566,177 RPS27P15, COX7A2, 118 more genes
    nsv6062138insertion1nstd212human GRCh38 chr6: 73,352,545-73,352,545 , GRCh37.p13 chr6: 74,062,268-74,062,268 DPPA5
    nsv5673923copy number variation1nstd102humanPathogenic GRCh37 chr6: 72,596,727-74,363,609 , GRCh38.p12 chr6: 71,887,024-73,653,886 LOC100422453, RPS27P15, 32 more genes
    nsv5626502insertion1nstd207human GRCh38 chr6: 73,352,499-73,352,499 , GRCh37.p13 chr6: 74,062,222-74,062,222 DPPA5
    nsv5465010copy number variation1nstd206human GRCh38 chr6: 73,324,000-73,364,977 , GRCh37.p13 chr6: 74,033,723-74,074,700 PAICSP3, KHDC3L, 1 more genes
    nsv5232363copy number variation1nstd204human GRCh38.p13 chr6: 73,323,901-73,711,800 , GRCh37.p13 chr6: 74,033,624-74,421,523 OOEP, RN7SL827P, 15 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

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