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 121

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5374684translocation1nstd200human GRCh38 chr14: 94,010,028-94,010,028 , GRCh38 chr14: 94,025,240-94,025,240 , GRCh37.p13 chr14: 94,476,374-94,476,374 , GRCh37.p13 chr14: 94,491,586-94,491,586 CCDC197, OTUB2
    nsv5374682translocation1nstd200human GRCh38 chr14: 94,003,089-94,003,089 , GRCh38 chr14: 94,025,248-94,025,248 , GRCh37.p13 chr14: 94,469,435-94,469,435 , GRCh37.p13 chr14: 94,491,594-94,491,594 CCDC197, OTUB2
    nsv4675107copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,783,523-96,907,490 , GRCh38.p12 chr14: 84,317,179-96,441,153 SHLD2P2, RPL15P2, 175 more genes
    nsv4510836mobile element insertion1nstd166human GRCh37.p13 chr14: 94,495,679-94,495,679 , GRCh38.p12 chr14: 94,029,333-94,029,333 , GRCh38.p12 chr14|NT_187601.1: 1,143,895-1,143,895 OTUB2
    nsv4456178copy number variation1nstd102humanPathogenic GRCh37 chr14: 91,969,028-107,285,437 , GRCh38.p12 chr14: 91,502,684-106,877,229 LOC105370639, SERPINA9, 600 more genes
    nsv4322697inversion1nstd166human GRCh37.p13 chr14: 93,328,296-94,706,279 , GRCh38.p12 chr14: 92,861,951-94,140,555 , GRCh38.p12 chr14|NT_187601.1: 1-1,354,504 ASB2, UNC79, 29 more genes
    nsv4217468copy number variation1nstd166human GRCh37.p13 chr14: 94,496,341-94,497,323 , GRCh38.p12 chr14|NT_187601.1: 1,144,557-1,145,539 , GRCh38.p12 chr14: 94,029,995-94,030,977 OTUB2
    nsv3922566copy number variation1nstd102humanPathogenic GRCh38 chr14: 90,255,156-95,274,696 , GRCh37 chr14: 90,721,500-95,741,033 , NCBI36 chr14: 89,791,253-94,810,786 RPSAP4, LOC105370622, 97 more genes
    nsv3922094copy number variation1nstd102humanPathogenic GRCh38 chr14: 73,655,772-106,879,298 , GRCh37 chr14: 74,122,475-107,287,505 , NCBI36 chr14: 73,192,228-106,358,550 LOC105370614, LOC105370617, 849 more genes
    nsv3921292copy number variation1nstd102humanPathogenic GRCh38 chr14: 91,455,861-106,832,642 , GRCh37 chr14: 91,922,205-107,240,869 , NCBI36 chr14: 90,991,958-106,311,914 IGHVII-15-1, LINC03117, 594 more genes
    nsv3919106copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482 SRMP2, IGHV3-71, 1929 more genes
    nsv3917422copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478 MIR656, TRAJ59, 1918 more genes
    nsv3915681copy number variation1nstd102humanPathogenic NCBI36 chr14: 76,758,891-106,358,550 , GRCh37 chr14: 77,689,138-107,287,505 , GRCh38 chr14: 77,222,795-106,879,298 IGHV3-32, SNORD114-31, 751 more genes
    nsv3914983copy number variation1nstd102humanPathogenic GRCh38 chr14: 86,094,030-106,832,642 , GRCh37 chr14: 86,560,374-107,240,869 , NCBI36 chr14: 85,630,127-106,311,914 IGHD5-5, EML5, 658 more genes
    nsv3914883copy number variation1nstd102humanPathogenic NCBI36 chr14: 92,077,081-104,401,040 , GRCh37 chr14: 93,007,328-105,329,995 , GRCh38 chr14: 92,540,983-104,863,658 LINC03117, EIF5, 360 more genes
    nsv3914418copy number variation1nstd102humanPathogenic NCBI36 chr14: 92,401,537-106,360,585 , GRCh37.p13 chr14: 93,331,784-107,289,540 , GRCh38.p12 chr14: 92,865,439-106,881,350 IGHVII-60-1, ATG2B, 582 more genes
    nsv3907460copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456 BANF1P1, IGHV1-68, 1996 more genes
    nsv3905673copy number variation1nstd102humanUncertain significance GRCh37 chr14: 93,498,930-96,059,698 , GRCh38.p12 chr14|NT_187601.1: 147,147-1,475,710 , GRCh38.p12 chr14: 93,207,711-95,593,361 GON7, LOC107984710, 65 more genes
    nsv3904265copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229 CRIP1, GPATCH2L, 1929 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