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 252

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974071inversion1nstd209human GRCh37.p13 chr7|NW_003871064.1: 478,880-2,946,547 , GRCh38 chr7: 72,949,644-75,417,311 , CLDN4, 79 more genes
    nsv5925548copy number variation1nstd209human GRCh38 chr7: 73,306,860-73,306,960 , GRCh37.p13 chr7: 72,720,856-72,720,956 , GRCh37.p13 chr7|NW_003871064.1: 836,096-836,196 NSUN5
    nsv5918891copy number variation1nstd209human GRCh38 chr7: 71,592,506-75,175,408 , GRCh37.p13 chr7|NW_003871064.1: 1-2,704,644 , GRCh37.p13 chr7: 71,935,722-74,527,751 , SPDYE10, 78 more genes
    nsv5852613copy number variation1nstd209human GRCh38 chr7: 73,298,370-73,310,235 , GRCh37.p13 chr7|NW_003871064.1: 827,606-839,471 , GRCh37.p13 chr7: 72,712,370-72,724,230 POM121B, NSUN5
    nsv5666565inversion1nstd207human GRCh38 chr7: 73,113,990-75,217,887 , GRCh37.p13 chr7|NW_003871064.1: 643,226-2,747,123 , CLDN4, 57 more genes
    nsv5580913copy number variation1nstd207human GRCh38 chr7: 73,302,804-73,302,855 , GRCh37.p13 chr7: 72,716,801-72,716,852 , GRCh37.p13 chr7|NW_003871064.1: 832,040-832,091 POM121B, NSUN5
    nsv5568606copy number variation1nstd207human GRCh38 chr7: 73,305,450-73,305,596 , GRCh37.p13 chr7: 72,719,447-72,719,593 , GRCh37.p13 chr7|NW_003871064.1: 834,686-834,832 NSUN5
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5484721copy number variation1nstd206human GRCh38 chr7: 73,306,860-73,306,969 , GRCh37.p13 chr7: 72,720,856-72,720,965 , GRCh37.p13 chr7|NW_003871064.1: 836,096-836,205 NSUN5
    nsv5381761copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 71,847,968-73,391,310 , GRCh38.p12 chr7: 72,382,983-73,976,980 CLDN4, CLDN3, 46 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4825062copy number variation1nstd200human GRCh37 chr7: 72,720,856-72,720,965 , GRCh38.p12 chr7: 73,306,860-73,306,969 NSUN5
    nsv4769380copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,717,369-74,142,224 , GRCh38.p12 chr7: 73,303,372-74,727,886 CLDN4, MLXIPL, 37 more genes
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4760625insertion1nstd199human GRCh37 chr7: 72,720,897-72,720,897 , GRCh38.p12 chr7: 73,306,901-73,306,901 NSUN5
    nsv4730256inversion12nstd198human GRCh38 chr7: 72,909,603-75,903,316 , GRCh37.p13 chr7|NW_003871064.1: 438,839-3,432,552 , CLDN4, 86 more genes
    nsv4729646copy number variation1nstd102humanPathogenic GRCh37 chr7: 68,977,230-73,939,510 , GRCh38.p12 chr7: 69,512,244-74,525,180 LOC105375346, ABHD11-AS1, 70 more genes
    nsv4729135copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,659,674-74,164,894 , GRCh38.p12 chr7: 73,245,641-74,750,557 CLIP2, ABHD11-AS1, 39 more genes
    nsv4728820copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,403,117-76,709,600 , GRCh38.p12 chr7: 72,932,579-77,080,283 FDPSP7, LOC105375352, 119 more genes
    nsv4684125copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,657,228-74,160,300 , GRCh38.p12 chr7: 73,243,195-74,745,961 GTF2I, DNAJC30, 39 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