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 172

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6664176copy number variation1nstd229human GRCh38 chr2: 24,111,416-24,117,169 , GRCh37.p13 chr2: 24,334,286-24,340,039 FAM228B, PFN4
    nsv6663543copy number variation1nstd229human GRCh38 chr2: 23,871,801-24,132,500 , GRCh37.p13 chr2: 24,094,671-24,355,370 SF3B6, WDCP, 12 more genes
    nsv6637009copy number variation1nstd102humanUncertain significance GRCh37 chr2: 23,908,436-24,636,185 , GRCh38.p12 chr2: 23,685,566-24,413,316 HMGN2P20, KLHL29, 19 more genes
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6628043copy number variation1nstd224human GRCh37 chr2: 24,344,072-24,538,088 , GRCh38.p12 chr2: 24,121,202-24,315,219 FAM228B, LOC105374328, 3 more genes
    nsv6628042copy number variation2nstd224human GRCh37 chr2: 24,342,446-24,538,088 , GRCh38.p12 chr2: 24,119,576-24,315,219 FAM228A, ITSN2, 3 more genes
    nsv6628041copy number variation1nstd224human GRCh37 chr2: 24,305,773-24,538,088 , GRCh38.p12 chr2: 24,082,903-24,315,219 TP53I3, ITSN2, 4 more genes
    nsv6627668copy number variation2nstd224human GRCh37 chr2: 24,334,361-24,540,632 , GRCh38.p12 chr2: 24,111,491-24,317,763 LOC105374328, FAM228B, 3 more genes
    nsv6627591copy number variation1nstd224human GRCh37 chr2: 24,334,361-24,495,796 , GRCh38.p12 chr2: 24,111,491-24,272,927 FAM228B, LOC105374328, 3 more genes
    nsv6536408inversion1nstd223human GRCh38 chr2: 24,116,579-24,117,016 , GRCh37.p13 chr2: 24,339,449-24,339,886 PFN4, FAM228B
    nsv6352331copy number variation1nstd223human GRCh38 chr2: 24,041,613-25,123,987 , GRCh37.p13 chr2: 24,264,483-25,346,856 LOC105377626, ADCY3, 25 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314937copy number variation1nstd102humanPathogenic GRCh37 chr2: 22,439,520-25,608,211 , GRCh38.p12 chr2: 22,216,648-25,385,342 ITSN2, POMC, 50 more genes
    nsv5988783copy number variation1nstd212human GRCh38 chr2: 24,094,681-24,327,768 , GRCh37.p13 chr2: 24,317,551-24,550,637 ITSN2, PFN4, 3 more genes
    nsv5881388copy number variation1nstd209human GRCh38 chr2: 24,094,681-24,327,763 , GRCh37.p13 chr2: 24,317,551-24,550,632 FAM228B, LOC105374328, 3 more genes
    nsv5283441copy number variation1nstd204human GRCh37.p13 chr2: 24,339,099-24,394,690 , GRCh38.p13 chr2: 24,116,229-24,171,821 PFN4, FAM228B, 1 more genes
    nsv5214760copy number variation1nstd204human GRCh38.p13 chr2: 24,116,201-24,171,800 , GRCh37.p13 chr2: 24,339,071-24,394,669 LOC105374328, PFN4, 1 more genes
    nsv5207885copy number variation1nstd204human GRCh38.p13 chr2: 24,115,474-24,150,474 , GRCh37.p13 chr2: 24,338,344-24,373,344 PFN4, FAM228B
    nsv5062279mobile element insertion1nstd203human GRCh38 chr2: 24,116,983-24,116,994 , GRCh37.p13 chr2: 24,339,853-24,339,864 PFN4, FAM228B
    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