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 181

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094410copy number variation1nstd102humanUncertain significance GRCh37 chr13: 51,484,213-52,602,726 , GRCh38.p12 chr13: 50,910,077-52,028,590 ATP7B, RNA5SP29, 29 more genes
    nsv6957409copy number variation1nstd229human GRCh38 chr13: 51,860,201-51,868,200 , GRCh37.p13 chr13: 52,434,337-52,442,336 CCDC70
    nsv6952289copy number variation1nstd229human GRCh38 chr13: 46,982,261-52,142,641 , GRCh37.p13 chr13: 47,556,396-52,716,777 KCNRG, RNA5SP28, 99 more genes
    nsv6951969copy number variation1nstd229human GRCh38 chr13: 45,143,357-52,624,108 , GRCh37.p13 chr13: 45,717,492-53,198,243 SNRPGP14, EBPL, 158 more genes
    nsv6948773copy number variation1nstd229human GRCh38 chr13: 51,860,168-51,868,185 , GRCh37.p13 chr13: 52,434,304-52,442,321 CCDC70
    nsv6944138copy number variation1nstd229human GRCh38 chr13: 49,633,124-51,990,526 , GRCh37.p13 chr13: 50,207,260-52,564,662 LOC107984561, RPL5P31, 50 more genes
    nsv6944015copy number variation1nstd229human GRCh38 chr13: 51,860,742-51,860,819 , GRCh37.p13 chr13: 52,434,878-52,434,955 CCDC70
    nsv6941985copy number variation1nstd229human GRCh38 chr13: 51,745,017-52,075,317 , GRCh37.p13 chr13: 52,319,153-52,649,453 UTP14C, DHRS12, 9 more genes
    nsv6938473copy number variation1nstd229human GRCh38 chr13: 51,742,952-52,015,459 , GRCh37.p13 chr13: 52,317,088-52,589,595 DHRS12, WDFY2, 7 more genes
    nsv6637534copy number variation1nstd102humanUncertain significance GRCh37 chr13: 52,024,106-52,496,419 , GRCh38.p12 chr13: 51,449,970-51,922,283 RNU6-65P, LOC107984561, 14 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
    nsv6622061copy number variation1nstd224human GRCh37 chr13: 52,367,207-52,439,890 , GRCh38.p12 chr13: 51,793,071-51,865,754 DHRS12, LOC107984561, 2 more genes
    nsv6621936copy number variation1nstd224human GRCh37 chr13: 52,100,822-52,440,184 , GRCh38.p12 chr13: 51,526,686-51,866,048 TMEM272, WDFY2, 8 more genes
    nsv6586711inversion1nstd223human GRCh38 chr13: 51,860,105-51,860,513 , GRCh37.p13 chr13: 52,434,241-52,434,649 CCDC70
    nsv6489538copy number variation1nstd223human GRCh38 chr13: 51,745,101-52,075,300 , GRCh37.p13 chr13: 52,319,237-52,649,436 UTP14C, NEK5, 9 more genes
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314198copy number variation1nstd102humanPathogenic GRCh37 chr13: 44,573,371-53,324,137 , GRCh38.p12 chr13: 43,999,235-52,750,002 PCNPP5, NRAD1, 189 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
    nsv6291680copy number variation1nstd102humanUncertain significance GRCh37 chr13: 52,024,030-52,496,419 , GRCh38.p12 chr13: 51,449,894-51,922,283 RN7SL413P, RNY1P6, 14 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