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 217

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5932186copy number variation1nstd209human GRCh38 chr13: 77,934,881-83,910,012 , GRCh37.p13 chr13: 78,509,016-84,484,147 NDFIP2, LINC01068, 54 more genes
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv4871044inversion1nstd200human GRCh37 chr13: 64,213,930-113,376,658 , GRCh38.p12 chr13: 63,639,797-112,722,344 , TUBGCP3, 564 more genes
    nsv4675995copy number variation1nstd102humanPathogenic GRCh37 chr13: 51,512,603-91,631,111 , GRCh38.p12 chr13: 50,938,467-90,978,857 RNU7-88P, LINC00564, 396 more genes
    nsv4675850copy number variation1nstd102humanPathogenic GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258 TEX30, LOC101927712, 680 more genes
    nsv4675244copy number variation1nstd102humanPathogenic GRCh37 chr13: 71,502,357-86,571,730 , GRCh38.p12 chr13: 70,928,225-85,997,595 RNU6-79P, LINC01069, 151 more genes
    nsv4606763copy number variation2nstd183human GRCh37 chr13: 79,175,030-79,176,563 , GRCh38.p12 chr13: 78,600,895-78,602,428 POU4F1, OBI1-AS1
    nsv4601854copy number variation1nstd183human GRCh37 chr13: 79,175,746-79,177,653 , GRCh38.p12 chr13: 78,601,611-78,603,518 OBI1-AS1, POU4F1
    nsv4598951copy number variation1nstd183human GRCh37 chr13: 79,177,063-79,336,741 , GRCh38.p12 chr13: 78,602,928-78,762,606 POU4F1, OBI1, 3 more genes
    nsv4456768copy number variation1nstd102humanUncertain significance GRCh37 chr13: 79,164,755-80,568,672 , GRCh38.p12 chr13: 78,590,620-79,994,537 RNA5SP33, LOC105370272, 20 more genes
    nsv4456561copy number variation1nstd102humanPathogenic GRCh37 chr13: 61,775,567-115,107,733 , GRCh38.p12 chr13: 61,201,433-114,342,258 LOC105370262, LINC01080, 609 more genes
    nsv4424086copy number variation1nstd174human GRCh37 chr13: 79,175,402-79,177,653 , GRCh38.p12 chr13: 78,601,267-78,603,518 POU4F1, OBI1-AS1
    nsv3965673insertion1nstd168human GRCh38 chr13: 78,600,193-78,601,625 , GRCh37.p13 chr13: 79,174,328-79,175,760 OBI1-AS1, POU4F1
    nsv3924676copy number variation1nstd102humanPathogenic GRCh38 chr13: 18,456,040-114,340,285 , GRCh37 chr13: 19,030,180-115,105,760 , NCBI36 chr13: 17,928,180-114,123,862 GRTP1, FABP5P1, 1334 more genes
    nsv3924528copy number variation1nstd102humanPathogenic GRCh37 chr13: 41,516,434-115,085,141 , GRCh38 chr13: 40,942,298-114,340,331 , NCBI36 chr13: 40,414,434-114,123,908 LOC105370271, OR7E33P, 925 more genes
    nsv3924390copy number variation1nstd102humanUncertain significance NCBI36 chr13: 78,030,831-78,786,536 , GRCh37.p13 chr13: 79,132,830-79,888,535 , GRCh38.p12 chr13: 78,558,695-79,314,400 OBI1, LINC00331, 12 more genes
    nsv3924212copy number variation1nstd102humanPathogenic NCBI36 chr13: 77,776,938-90,734,195 , GRCh37 chr13: 78,878,937-91,936,194 , GRCh38 chr13: 78,304,802-91,283,940 DDX6P2, GRPEL2P1, 117 more genes
    nsv3924052copy number variation1nstd102humanPathogenic GRCh38 chr13: 41,288,493-85,137,552 , NCBI36 chr13: 40,760,629-84,609,688 , GRCh37 chr13: 41,862,629-85,711,687 TMEM272, LOC105370241, 535 more genes
    nsv3923692copy number variation1nstd102humanPathogenic NCBI36 chr13: 76,533,916-91,910,660 , GRCh37 chr13: 77,635,915-93,112,659 , GRCh38 chr13: 77,061,780-92,460,406 UBE2D3P4, RPL21P111, 145 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