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 238

    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
    nsv7093904copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,344,461-105,992,004 , GRCh38.p12 chr10: 97,584,704-104,232,246 ABCC2, LBX1-AS1, 160 more genes
    nsv7061664inversion1nstd229human GRCh38 chr10: 99,665,184-99,668,710 , GRCh37.p13 chr10: 101,424,941-101,428,467 ENTPD7
    nsv7059886inversion1nstd229human GRCh38 chr10: 95,520,399-102,687,169 , GRCh37.p13 chr10: 97,280,156-104,446,926 , ENTPD1-AS1, 168 more genes
    nsv6894164copy number variation1nstd229human GRCh38 chr10: 99,674,054-99,684,742 , GRCh37.p13 chr10: 101,433,811-101,444,499 ENTPD7
    nsv6892116copy number variation1nstd229human GRCh38 chr10: 99,663,401-99,706,800 , GRCh37.p13 chr10: 101,423,158-101,466,557 EBAG9P1, ENTPD7, 1 more genes
    nsv6891025copy number variation1nstd229human GRCh38 chr10: 99,654,956-99,659,956 , GRCh37.p13 chr10: 101,414,713-101,419,713 ENTPD7, SLC25A28
    nsv6890065copy number variation1nstd229human GRCh38 chr10: 99,671,320-99,678,077 , GRCh37.p13 chr10: 101,431,077-101,437,834 ENTPD7
    nsv6887373copy number variation1nstd229human GRCh38 chr10: 99,662,001-99,688,400 , GRCh37.p13 chr10: 101,421,758-101,448,157 ENTPD7
    nsv6885635copy number variation1nstd229human GRCh38 chr10: 99,675,439-99,680,076 , GRCh37.p13 chr10: 101,435,196-101,439,833 ENTPD7
    nsv6885620copy number variation1nstd229human GRCh38 chr10: 99,710,574-99,714,849 , GRCh37.p13 chr10: 101,470,331-101,474,606 COX15, ENTPD7
    nsv6884993copy number variation1nstd229human GRCh38 chr10: 99,661,966-99,688,452 , GRCh37.p13 chr10: 101,421,723-101,448,209 ENTPD7
    nsv6884903copy number variation1nstd229human GRCh38 chr10: 99,661,101-99,693,500 , GRCh37.p13 chr10: 101,420,858-101,453,257 COX15, ENTPD7
    nsv6881964copy number variation1nstd229human GRCh38 chr10: 99,645,866-99,659,747 , GRCh37.p13 chr10: 101,405,623-101,419,504 SLC25A28, LOC105378450, 1 more genes
    nsv6880398copy number variation1nstd229human GRCh38 chr10: 99,661,201-99,693,200 , GRCh37.p13 chr10: 101,420,958-101,452,957 ENTPD7, COX15
    nsv6880127copy number variation1nstd229human GRCh38 chr10: 99,711,540-100,023,720 , GRCh37.p13 chr10: 101,471,297-101,783,477 NANOGP6, ENTPD7, 5 more genes
    nsv6879290copy number variation1nstd229human GRCh38 chr10: 99,685,982-99,687,236 , GRCh37.p13 chr10: 101,445,739-101,446,993 ENTPD7
    nsv6595106inversion1nstd223human GRCh38 chr10: 92,377,901-102,079,487 , GRCh37.p13 chr10: 94,137,658-103,839,244 , ARHGAP19, 201 more genes
    nsv6590247inversion1nstd223human GRCh38 chr10: 99,701,295-99,702,058 , GRCh37.p13 chr10: 101,461,052-101,461,815 COX15, ENTPD7
    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