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 100

    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
    nsv6437560copy number variation1nstd223human GRCh38 chr10: 73,673,561-73,872,094 , GRCh37.p13 chr10: 75,433,319-75,631,852 CAMK2G, FUT11, 12 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
    nsv6132050copy number variation1nstd213human GRCh37 chr10: 75,330,000-75,750,001 , GRCh38.p12 chr10: 73,570,242-73,990,243 CAMK2G, GLUD1P3, 18 more genes
    nsv5909992copy number variation1nstd209human GRCh38 chr10: 72,964,663-80,533,256 , GRCh37.p13 chr10: 74,724,421-82,293,012 , PRXL2A, 155 more genes
    nsv5301974copy number variation1nstd204human GRCh38.p13 chr10: 73,709,242-74,768,785 , GRCh37.p13 chr10: 75,469,000-76,528,543 , RPSAP6, 24 more genes
    nsv5259208copy number variation1nstd204human GRCh37.p13 chr10: 75,539,845-75,573,415 , GRCh38.p13 chr10: 73,780,087-73,813,657 CAMK2G, NDST2, 4 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
    nsv4973772copy number variation1nstd200human GRCh38 chr10: 73,709,251-74,768,777 , GRCh37.p13 chr10: 75,469,009-76,528,535 , AP3M1, 24 more genes
    nsv4973771copy number variation1nstd200human GRCh38 chr10: 73,673,558-73,872,096 , GRCh37.p13 chr10: 75,433,316-75,631,854 FUT11, CAMK2G, 12 more genes
    nsv4839922copy number variation1nstd200human GRCh37 chr10: 75,469,009-76,528,535 , GRCh38.p12 chr10: 73,709,251-74,768,777 , NDUFA8P1, 24 more genes
    nsv4612245copy number variation1nstd183human GRCh37 chr10: 75,542,067-75,546,631 , GRCh38.p12 chr10: 73,782,309-73,786,873 LOC107984243, CHCHD1, 1 more genes
    nsv4456093copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,251,395-75,763,287 , GRCh38.p12 chr10: 73,491,637-74,003,529 ZSWIM8-AS1, PPP3CB-AS1, 23 more genes
    nsv4422261copy number variation1nstd174human GRCh37 chr10: 75,475,447-75,682,321 , GRCh38.p12 chr10: 73,715,689-73,922,563 GLUD1P3, ZSWIM8, 12 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
    nsv3970760insertion1nstd168human GRCh38 chr10: 73,774,242-73,796,385 , GRCh37.p13 chr10: 75,534,000-75,556,143 ZSWIM8, CHCHD1, 3 more genes
    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
    nsv3922335copy number variation1nstd102humanPathogenic GRCh37 chr10: 60,196,226-76,174,974 , GRCh38 chr10: 58,436,466-74,415,216 , NCBI36 chr10: 59,866,232-75,844,980 UNC5B-AS1, ALDH7A1P4, 250 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