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 267

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094404copy number variation1nstd102humanUncertain significance GRCh37 chr13: 36,888,344-36,888,578 , GRCh38.p12 chr13: 36,314,207-36,314,441 SPART
    nsv7059353inversion1nstd229human GRCh38 chr13: 36,334,388-36,334,575 , GRCh37.p13 chr13: 36,908,525-36,908,712 SPART
    nsv7058180inversion1nstd229human GRCh38 chr13: 29,278,598-37,954,955 , GRCh37.p13 chr13: 29,852,735-38,529,092 ZAR1L, HSPH1, 116 more genes
    nsv6945452copy number variation1nstd229human GRCh38 chr13: 36,280,621-36,301,108 , GRCh37.p13 chr13: 36,854,758-36,875,245 CCDC169-SOHLH2, SPART, 1 more genes
    nsv6945033copy number variation1nstd229human GRCh38 chr13: 36,265,801-36,302,400 , GRCh37.p13 chr13: 36,839,938-36,876,537 CCDC169, SPART, 2 more genes
    nsv6943315copy number variation1nstd229human GRCh38 chr13: 36,332,040-36,332,081 , GRCh37.p13 chr13: 36,906,177-36,906,218 SPART
    nsv6940946copy number variation1nstd229human GRCh38 chr13: 36,337,926-36,340,518 , GRCh37.p13 chr13: 36,912,063-36,914,655 SPART
    nsv6940259copy number variation1nstd229human GRCh38 chr13: 36,336,414-36,336,512 , GRCh37.p13 chr13: 36,910,551-36,910,649 SPART
    nsv6939391copy number variation1nstd229human GRCh38 chr13: 36,362,013-36,363,573 , GRCh37.p13 chr13: 36,936,150-36,937,710 SPART, SPART-AS1
    nsv6637985copy number variation1nstd102humanUncertain significance GRCh37 chr13: 36,148,057-41,670,428 , GRCh38.p12 chr13: 35,573,920-41,096,292 RPS12P24, SPART, 86 more genes
    nsv6637238copy number variation1nstd102humanPathogenic GRCh37 chr13: 35,501,428-40,901,176 , GRCh38.p12 chr13: 34,927,291-40,327,039 CCDC169-SOHLH2, RNA5SP26, 74 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6622043copy number variation1nstd224human GRCh37 chr13: 36,813,522-37,199,122 , GRCh38.p12 chr13: 36,239,385-36,624,985 CCNA1, SPART, 5 more genes
    nsv6592509inversion1nstd223human GRCh38 chr13: 36,347,330-36,348,024 , GRCh37.p13 chr13: 36,921,467-36,922,161 SPART-AS1, SPART
    nsv6487250copy number variation1nstd223human GRCh38 chr13: 36,343,901-36,349,300 , GRCh37.p13 chr13: 36,918,038-36,923,437 SPART-AS1, SPART
    nsv6487009copy number variation1nstd223human GRCh38 chr13: 36,315,901-36,321,600 , GRCh37.p13 chr13: 36,890,038-36,895,737 SPART
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314117copy number variation1nstd102humanPathogenic GRCh37 chr13: 36,376,204-80,681,753 , GRCh38.p12 chr13: 35,802,067-80,107,618 RBM26, RNY4P31, 591 more genes
    nsv6314030copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251 RPSAP53, LOC105370213, 1310 more genes
    nsv6289999copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 LINC00363, LOC105370118, 1334 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