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 187

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137192copy number variation1nstd102humanUncertain significance GRCh37 chr2: 232,520,701-234,168,331 , GRCh38.p12 chr2: 231,655,990-233,259,685 NEU2, MIR562, 38 more genes
    nsv7049654inversion1nstd229human GRCh38 chr2: 233,236,665-233,574,597 , GRCh37.p13 chr2: 234,145,311-234,483,243 DGKD, SAG, 5 more genes
    nsv7041487inversion1nstd229human GRCh38 chr2: 233,277,178-233,725,509 , GRCh37.p13 chr2: 234,185,824-234,634,155 SCARNA6, UGT1A5, 16 more genes
    nsv6695695copy number variation1nstd229human GRCh38 chr2: 233,232,967-233,543,299 , GRCh37.p13 chr2: 234,141,613-234,451,945 USP40, SCARNA5, 4 more genes
    nsv6695110copy number variation1nstd229human GRCh38 chr2: 233,112,247-233,292,742 , GRCh37.p13 chr2: 233,976,957-234,201,388 SCARNA6, ATG16L1, 3 more genes
    nsv6694251copy number variation1nstd229human GRCh38 chr2: 233,277,028-233,460,169 , GRCh37.p13 chr2: 234,185,674-234,368,815 ATG16L1, SCARNA6, 2 more genes
    nsv6691671copy number variation1nstd229human GRCh38 chr2: 232,868,845-233,267,287 , GRCh37.p13 chr2: 233,733,555-234,175,933 NEU2, LOC101928881, 5 more genes
    nsv6689588copy number variation1nstd229human GRCh38 chr2: 233,275,591-233,335,266 , GRCh37.p13 chr2: 234,184,237-234,243,912 SCARNA5, ATG16L1, 2 more genes
    nsv6689535copy number variation1nstd229human GRCh38 chr2: 233,283,535-233,288,146 , GRCh37.p13 chr2: 234,192,181-234,196,792 ATG16L1, SCARNA6
    nsv6689043copy number variation1nstd229human GRCh38 chr2: 233,061,229-233,370,687 , GRCh37.p13 chr2: 233,925,939-234,279,333 INPP5D, SAG, 5 more genes
    nsv6686173copy number variation1nstd229human GRCh38 chr2: 233,271,953-233,322,386 , GRCh37.p13 chr2: 234,180,599-234,231,032 ATG16L1, SAG, 2 more genes
    nsv6679072copy number variation1nstd229human GRCh38 chr2: 233,093,901-233,643,200 , GRCh37.p13 chr2: 233,958,611-234,551,846 DGKD, INPP5D, 12 more genes
    nsv6636912copy number variation1nstd102humanUncertain significance GRCh37 chr2: 233,642,145-237,654,870 , GRCh38.p12 chr2: 232,777,435-236,746,227 UGT1A, SH3BP4, 70 more genes
    nsv6628068copy number variation1nstd224human GRCh37 chr2: 234,178,662-234,255,047 , GRCh38.p12 chr2: 233,270,016-233,346,401 , GRCh38.p12 chr2|NW_011332690.1: 215,354-291,739 SAG, ATG16L1, 2 more genes
    nsv6338498copy number variation1nstd223human GRCh38 chr2: 233,275,591-233,335,263 , GRCh37.p13 chr2: 234,184,237-234,243,909 ATG16L1, SAG, 2 more genes
    nsv6315436copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,227,837-242,783,384 , GRCh38.p12 chr2: 232,363,127-241,841,232 LOC105373929, LOC105373932, 204 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313683copy number variation1nstd102humanPathogenic GRCh37 chr2: 228,807,574-235,475,892 , GRCh38.p12 chr2: 227,942,858-234,567,248 RNU7-9P, SCARNA5, 143 more genes
    nsv6313668copy number variation1nstd102humanPathogenic GRCh37 chr2: 219,606,537-239,217,703 , GRCh38.p12 chr2: 218,741,814-238,309,062 LOC105373947, RN7SL764P, 357 more genes
    nsv6311650copy number variation2nstd102humanUncertain significance GRCh37 chr2: 231,033,840-234,978,657 , GRCh38.p12 chr2: 230,169,124-234,070,013 SP110, LINC00471, 112 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