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 89

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7066606inversion1nstd229human GRCh38 chr10: 67,967,096-68,456,909 , GRCh37.p13 chr10: 69,726,853-70,216,666 MYPN, RUFY2, 12 more genes
    nsv6889510copy number variation1nstd229human GRCh38 chr10: 68,226,881-68,229,023 , GRCh37.p13 chr10: 69,986,638-69,988,780 ATOH7
    nsv6637795copy number variation1nstd102humanUncertain significance GRCh37 chr10: 69,824,933-70,064,085 , GRCh38.p12 chr10: 68,065,176-68,304,328 MYPN, KRT19P4, 6 more genes
    nsv6637232copy number variation1nstd102humanUncertain significance GRCh37 chr10: 69,824,933-70,070,858 , GRCh38.p12 chr10: 68,065,176-68,311,101 HERC4, PBLD, 6 more genes
    nsv6314185copy number variation1nstd102humanPathogenic GRCh37 chr10: 68,735,254-78,885,714 , GRCh38.p12 chr10: 66,975,496-77,125,956 SLC25A16, CTNNA3, 204 more genes
    nsv6308916copy number variation1nstd102humanUncertain significance GRCh37 chr10: 67,680,088-71,332,799 , GRCh38.p12 chr10: 65,920,330-69,573,043 RPS3AP38, MIR7151, 62 more genes
    nsv6131803copy number variation1nstd213human GRCh37 chr10: 69,830,000-70,290,001 , GRCh38.p12 chr10: 68,070,243-68,530,244 SLC25A16, RPL26P29, 13 more genes
    nsv5485238copy number variation1nstd206human GRCh38 chr10: 67,980,241-68,318,477 , GRCh37.p13 chr10: 69,739,998-70,078,234 RN7SKP202, POU5F1P5, 8 more genes
    nsv5243486copy number variation1nstd204human GRCh38.p13 chr10: 68,209,901-68,601,300 , GRCh37.p13 chr10: 69,969,658-70,361,057 LINC02640, RPL26P27, 12 more genes
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4675581copy number variation1nstd102humanUncertain significance GRCh37 chr10: 69,066,516-70,079,295 , GRCh38.p12 chr10: 67,306,758-68,319,538 RN7SL220P, TRS-TGA1-1, 22 more genes
    nsv4457126copy number variation1nstd102humanUncertain significance GRCh37 chr10: 69,867,056-69,989,788 , GRCh38.p12 chr10: 68,107,299-68,230,031 ATOH7, LOC107984240, 2 more genes
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4184916copy number variation1nstd166human GRCh37.p13 chr10: 69,986,629-69,988,784 , GRCh38.p12 chr10: 68,226,872-68,229,027 ATOH7
    nsv4180759copy number variation1nstd166human GRCh37.p13 chr10: 69,263,643-70,077,786 , GRCh38.p12 chr10: 67,503,885-68,318,029 RPL21P92, RNU6-1250P, 20 more genes
    nsv4175396copy number variation1nstd166human GRCh37.p13 chr10: 69,992,138-69,992,573 , GRCh38.p12 chr10: 68,232,381-68,232,816 ATOH7
    nsv3924859copy number variation1nstd102humanPathogenic NCBI36 chr10: 52,159,133-88,896,941 , GRCh38 chr10: 50,729,367-87,147,204 , GRCh37 chr10: 52,489,127-88,906,961 BMS1P4-AGAP5, MTCO2P23, 471 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