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 74

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5914382copy number variation1nstd209human GRCh38 chr10: 27,312,316-36,846,398 , GRCh37.p13 chr10: 27,601,245-37,135,326 , RN7SL241P, 160 more genes
    nsv5126027mobile element insertion1nstd203human GRCh38 chr10: 29,600,834-29,600,844 , GRCh37.p13 chr10: 29,889,763-29,889,773 SVIL, MIR938
    nsv4983915copy number variation1nstd200human GRCh38 chr10: 29,599,986-29,618,300 , GRCh37.p13 chr10: 29,888,915-29,907,229 SVIL, MIR938
    nsv4833356copy number variation1nstd200human GRCh37 chr10: 29,888,915-29,907,229 , GRCh38.p12 chr10: 29,599,986-29,618,300 MIR938, SVIL
    nsv4680495copy number variation1nstd189human GRCh37.p13 chr10: 29,866,139-30,340,823 , GRCh38.p12 chr10: 29,577,210-30,051,894 SVIL, JCAD, 9 more genes
    nsv4674851copy number variation1nstd102humanUncertain significance GRCh37 chr10: 29,204,926-30,604,037 , GRCh38.p12 chr10: 28,915,997-30,315,108 EEF1A1P39, LOC107984173, 25 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
    nsv4182763copy number variation1nstd166human GRCh37.p13 chr10: 29,890,411-29,891,357 , GRCh38.p12 chr10: 29,601,482-29,602,428 MIR938, SVIL
    nsv3921533copy number variation1nstd102humanPathogenic GRCh37 chr10: 28,056,899-30,335,014 , NCBI36 chr10: 28,096,905-30,375,020 , GRCh38 chr10: 27,767,970-30,046,085 ODAD2, LOC107984170, 48 more genes
    nsv3920796copy number variation1nstd102humanPathogenic NCBI36 chr10: 62,842-35,729,127 , GRCh37.p13 chr10: 72,842-35,689,121 , GRCh38.p12 chr10: 26,906-35,400,193 EPC1-AS1, RNU6-452P, 559 more genes
    nsv3920598copy number variation1nstd102humanBenign NCBI36 chr10: 4,636,926-47,125,152 , GRCh38 chr10: 4,604,734-48,074,662 , GRCh37 chr10: 4,646,926-47,531,169 LOC100420467, LOC105376474, 709 more genes
    nsv3915584copy number variation1nstd102humanPathogenic GRCh38 chr10: 27,046,685-30,228,891 , GRCh37 chr10: 27,335,614-30,517,820 , NCBI36 chr10: 27,375,620-30,557,826 TRIAP1P1, LOC112268060, 70 more genes
    nsv3911634copy number variation1nstd102humanLikely pathogenic NCBI36 chr10: 19,417,096-33,061,227 , GRCh37 chr10: 19,377,090-33,021,221 , GRCh38 chr10: 19,088,161-32,732,293 BMI1, CCND3P1, 221 more genes
    nsv3911283copy number variation1nstd102humanPathogenic GRCh37 chr10: 27,111,945-30,537,855 , NCBI36 chr10: 27,151,951-30,577,861 , GRCh38 chr10: 26,823,016-30,248,926 YME1L1, SVIL, 72 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 LOC100419870, LOC102724439, 2105 more genes
    nsv3905007copy number variation1nstd102humanLikely benign GRCh37 chr10: 29,849,273-30,352,152 , GRCh38.p12 chr10: 29,560,344-30,063,223 JCAD, LOC107984218, 10 more genes
    nsv3904390copy number variation1nstd102humanPathogenic GRCh37 chr10: 100,026-50,961,640 , GRCh38.p12 chr10: 54,086-49,753,594 LINC00700, LINC02881, 806 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 ANXA11, EDRF1-DT, 2085 more genes
    nsv3891958copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414 TUBB8, PPP2R2D, 2085 more genes
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 AGAP14P, LOC100505502, 2097 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