U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 33

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6314353complex chromosomal rearrangement11nstd102humanLikely pathogenic GRCh37 chr3: 152,159,406-152,159,406 , GRCh37 chr7: 119,889,690-119,889,690 , GRCh37 chr7: 119,999,919-119,999,919 , GRCh37 chr7: 120,004,010-120,004,010 , GRCh37 chr7: 120,765,008-120,765,008 , GRCh37 chr3: 152,159,406-152,159,406 , GRCh37 chr7: 119,646,829-119,646,829 , GRCh37 chr7: 119,646,830-119,646,830 , GRCh37 chr7: 119,889,673-119,889,673 , GRCh37 chr7: 122,606,486-122,606,486 , GRCh37 chr5: 87,073,891-87,073,891 , GRCh37 chr7: 119,995,774-119,995,774 , GRCh37 chr7: 120,004,011-120,004,011 , GRCh37 chr7: 120,254,240-120,254,240 , GRCh37 chr7: 120,766,450-120,766,450 , GRCh37 chr3: 155,627,600-155,627,600 , GRCh37 chr3: 155,627,601-155,627,601 , GRCh37 chr5: 87,073,908-87,073,908 , GRCh37 chr7: 119,995,779-119,995,779 , GRCh37 chr7: 119,999,922-119,999,922 , GRCh37 chr7: 120,254,239-120,254,239 , GRCh37 chr7: 122,606,556-122,606,556 , GRCh38.p12 chr3: 152,441,617-152,441,617 , GRCh38.p12 chr7: 120,355,725-120,355,725 , GRCh38.p12 chr7: 120,359,868-120,359,868 , GRCh38.p12 chr7: 120,614,185-120,614,185 , GRCh38.p12 chr7: 121,124,954-121,124,954 , GRCh38.p12 chr7: 122,966,502-122,966,502 , GRCh38.p12 chr3: 152,441,617-152,441,617 , GRCh38.p12 chr5: 87,778,091-87,778,091 , GRCh38.p12 chr7: 120,355,720-120,355,720 , GRCh38.p12 chr7: 120,363,957-120,363,957 , GRCh38.p12 chr7: 120,614,186-120,614,186 , GRCh38.p12 chr5: 87,778,074-87,778,074 , GRCh38.p12 chr7: 120,249,636-120,249,636 , GRCh38.p12 chr7: 120,359,865-120,359,865 , GRCh38.p12 chr3: 155,909,811-155,909,811 , GRCh38.p12 chr3: 155,909,812-155,909,812 , GRCh38.p12 chr7: 120,006,775-120,006,775 , GRCh38.p12 chr7: 120,006,776-120,006,776 , GRCh38.p12 chr7: 120,249,619-120,249,619 , GRCh38.p12 chr7: 120,363,956-120,363,956 , GRCh38.p12 chr7: 121,126,396-121,126,396 , GRCh38.p12 chr7: 122,966,432-122,966,432 CPED1, KCND2, 3 more genes
    nsv6290850copy number variation1nstd102humanLikely benign GRCh37 chr7: 120,632,159-120,893,340 , GRCh38.p12 chr7: 120,992,105-121,253,286 CPED1, RNU6-517P, 2 more genes
    nsv3894074copy number variation1nstd102humanLikely benign GRCh37 chr7: 120,864,414-121,086,762 , GRCh38.p12 chr7: 121,224,360-121,446,708 CPED1, RPL18P4, 3 more genes
    nsv3915482copy number variation1nstd102humanBenign NCBI36 chr7: 120,455,174-120,674,536 , GRCh37 chr7: 120,667,938-120,887,300 , GRCh38 chr7: 121,027,884-121,247,246 CPED1, RNA5SP241, 2 more genes
    nsv3897553copy number variation1nstd102humanBenign GRCh37 chr7: 120,560,714-120,705,300 , GRCh38.p12 chr7: 120,920,660-121,065,246 CPED1, HMGN1P18, 2 more genes
    nsv3907256copy number variation1nstd102humanUncertain significance GRCh37 chr7: 120,632,159-120,897,181 , GRCh38.p12 chr7: 120,992,105-121,257,127 CPED1, HMGN1P18, 2 more genes
    nsv3923564copy number variation1nstd102humanUncertain significance NCBI36 chr7: 120,594,858-120,831,965 , GRCh37.p13 chr7: 120,807,622-121,044,729 , GRCh38.p12 chr7: 121,167,568-121,404,675 CPED1, FAM3C, 3 more genes
    nsv6290807copy number variation1nstd102humanUncertain significance GRCh37 chr7: 120,813,156-121,033,289 , GRCh38.p12 chr7: 121,173,102-121,393,235 CPED1, FAM3C, 2 more genes
    nsv4456742copy number variation1nstd102humanUncertain significance GRCh37 chr7: 120,818,380-121,033,193 , GRCh38.p12 chr7: 121,178,326-121,393,139 CPED1, RNU6-517P, 2 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 CPED1, RNU6-438P, 2682 more genes
    nsv3888815copy number variation1nstd102humanPathogenic GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467 CPED1, LOC107986817, 2014 more genes
    nsv3924380copy number variation1nstd102humanPathogenic GRCh37 chr7: 101,912,320-120,918,695 , GRCh38 chr7: 102,196,924-121,278,641 , NCBI36 chr7: 101,626,924-120,705,931 CPED1, LOC102724434, 222 more genes
    nsv3916726copy number variation1nstd102humanPathogenic NCBI36 chr7: 116,754,095-134,125,980 , GRCh38 chr7: 117,326,805-134,790,689 , GRCh37 chr7: 116,966,859-134,475,440 CPED1, LOC107986845, 245 more genes
    nsv4675322copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,617,406-123,217,914 , GRCh38.p12 chr7: 106,976,961-123,577,860 CPED1, CBLL1-AS1, 168 more genes
    nsv3900620copy number variation1nstd102humanPathogenic GRCh37 chr7: 111,613,396-127,897,316 , GRCh38.p12 chr7: 111,973,341-128,257,263 CPED1, LSM8, 170 more genes
    nsv3923570copy number variation1nstd102humanPathogenic NCBI36 chr7: 107,583,881-122,963,817 , GRCh37.p13 chr7: 107,796,645-123,176,581 , GRCh38.p12 chr7: 108,156,200-123,536,527 CPED1, ANKRD7, 142 more genes
    nsv3916529copy number variation1nstd102humanPathogenic GRCh37 chr7: 113,782,532-125,480,435 , NCBI36 chr7: 113,569,768-125,267,671 , GRCh38 chr7: 114,142,477-125,840,381 CPED1, CAPZA2, 124 more genes
    nsv3922792copy number variation1nstd102humanPathogenic NCBI36 chr7: 113,227,126-124,326,508 , GRCh37 chr7: 113,439,890-124,539,272 , GRCh38 chr7: 113,799,835-124,899,218 CPED1, MTND4P6, 116 more genes
    nsv5381759copy number variation1nstd102humanPathogenic GRCh37 chr7: 116,297,277-126,370,694 , GRCh38.p12 chr7: 116,657,223-126,730,640 CPED1, TMEM229A, 110 more genes
    nsv3894780copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842 CPED1, RNU6-565P, 2684 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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