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 151

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7096604copy number variation1nstd102humanPathogenic GRCh37 chr2: 210,636,797-213,403,254 , GRCh38.p12 chr2: 209,772,073-212,538,530 MTCO1P46, LOC100420775, 19 more genes
    nsv7053023inversion1nstd229human GRCh38 chr2: 212,286,605-212,549,169 , GRCh37.p13 chr2: 213,151,330-213,413,893 MIR548F2, ERBB4
    nsv6696018copy number variation1nstd229human GRCh38 chr2: 212,417,754-212,458,470 , GRCh37.p13 chr2: 213,282,478-213,323,194 MIR548F2, ERBB4
    nsv6696012copy number variation1nstd229human GRCh38 chr2: 212,138,301-212,504,700 , GRCh37.p13 chr2: 213,003,026-213,369,424 ERBB4, MIR548F2
    nsv6695542copy number variation1nstd229human GRCh38 chr2: 212,362,356-212,436,421 , GRCh37.p13 chr2: 213,227,080-213,301,145 ERBB4, MIR548F2
    nsv6691759copy number variation1nstd229human GRCh38 chr2: 212,391,308-212,513,130 , GRCh37.p13 chr2: 213,256,032-213,377,854 ERBB4, MIR548F2
    nsv6689536copy number variation1nstd229human GRCh38 chr2: 212,238,301-212,504,800 , GRCh37.p13 chr2: 213,103,026-213,369,524 MIR548F2, ERBB4
    nsv6687037copy number variation1nstd229human GRCh38 chr2: 212,348,345-212,495,706 , GRCh37.p13 chr2: 213,213,069-213,360,430 ERBB4, MIR548F2
    nsv6686962copy number variation1nstd229human GRCh38 chr2: 212,417,901-212,492,300 , GRCh37.p13 chr2: 213,282,625-213,357,024 MIR548F2, ERBB4
    nsv6686296copy number variation1nstd229human GRCh38 chr2: 212,380,801-212,474,700 , GRCh37.p13 chr2: 213,245,525-213,339,424 ERBB4, MIR548F2
    nsv6684057copy number variation1nstd229human GRCh38 chr2: 212,401,954-212,529,399 , GRCh37.p13 chr2: 213,266,678-213,394,123 ERBB4, MIR548F2
    nsv6681083copy number variation1nstd229human GRCh38 chr2: 212,240,901-212,504,900 , GRCh37.p13 chr2: 213,105,626-213,369,624 MIR548F2, ERBB4
    nsv6678347copy number variation1nstd229human GRCh38 chr2: 212,420,146-212,434,959 , GRCh37.p13 chr2: 213,284,870-213,299,683 ERBB4, MIR548F2
    nsv6678314copy number variation1nstd229human GRCh38 chr2: 212,372,901-212,505,000 , GRCh37.p13 chr2: 213,237,625-213,369,724 ERBB4, MIR548F2
    nsv6636851copy number variation1nstd102humanUncertain significance GRCh37 chr2: 212,597,211-213,804,569 , GRCh38.p12 chr2: 211,732,486-212,939,845 MIR4776-2, MTCO1P46, 8 more genes
    nsv6636518copy number variation1nstd102humanUncertain significance GRCh37 chr2: 213,290,522-214,539,066 , GRCh38.p12 chr2: 212,425,798-213,674,342 LOC105373864, SPAG16, 12 more genes
    nsv6627992copy number variation1nstd224human GRCh37 chr2: 212,604,921-213,788,891 , GRCh38.p12 chr2: 211,740,196-212,924,167 ERBB4, PCED1CP, 4 more genes
    nsv6627621copy number variation1nstd224human GRCh37 chr2: 213,113,140-213,292,049 , GRCh38.p12 chr2: 212,248,415-212,427,325 ERBB4, MIR548F2
    nsv6547266inversion1nstd223human GRCh38 chr2: 211,965,645-212,501,180 , GRCh37.p13 chr2: 212,830,370-213,365,904 MIR548F2, ERBB4
    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