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 137

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054895inversion1nstd229human GRCh38 chr2: 229,787,965-232,576,060 , GRCh37.p13 chr2: 230,652,681-233,440,770 GPR55, RN7SL834P, 80 more genes
    nsv7049703inversion1nstd229human GRCh38 chr2: 230,842,839-230,865,190 , GRCh37.p13 chr2: 231,707,554-231,729,905 ITM2C
    nsv7047313inversion1nstd229human GRCh38 chr2: 230,865,900-230,871,719 , GRCh37.p13 chr2: 231,730,615-231,736,434 ITM2C
    nsv7039246inversion1nstd229human GRCh38 chr2: 230,817,971-230,981,097 , GRCh37.p13 chr2: 231,682,686-231,845,812 GPR55, COX20P2, 3 more genes
    nsv6693043copy number variation1nstd229human GRCh38 chr2: 230,829,401-231,058,500 , GRCh37.p13 chr2: 231,694,116-231,923,214 C2orf72, SPATA3, 7 more genes
    nsv6690800copy number variation1nstd229human GRCh38 chr2: 230,871,090-230,874,421 , GRCh37.p13 chr2: 231,735,805-231,739,136 ITM2C
    nsv6684407copy number variation1nstd229human GRCh38 chr2: 230,875,730-230,878,892 , GRCh37.p13 chr2: 231,740,445-231,743,607 ITM2C
    nsv6681323copy number variation1nstd229human GRCh38 chr2: 230,878,161-230,878,239 , GRCh37.p13 chr2: 231,742,876-231,742,954 ITM2C
    nsv6678540copy number variation1nstd229human GRCh38 chr2: 230,799,348-230,905,503 , GRCh37.p13 chr2: 231,664,063-231,770,218 CAB39, GCSIR, 2 more genes
    nsv6628009copy number variation1nstd224human GRCh37 chr2: 231,726,018-231,738,269 , GRCh38.p12 chr2: 230,861,303-230,873,554 ITM2C
    nsv6353118copy number variation1nstd223human GRCh38 chr2: 230,850,236-230,862,898 , GRCh37.p13 chr2: 231,714,951-231,727,613 ITM2C
    nsv6343918copy number variation1nstd223human GRCh38 chr2: 230,871,258-230,871,934 , GRCh37.p13 chr2: 231,735,973-231,736,649 ITM2C
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313761copy number variation1nstd102humanPathogenic GRCh37 chr2: 229,968,217-231,883,182 , GRCh38.p12 chr2: 229,103,501-231,018,467 SLC16A14, BANF1P3, 35 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
    nsv6253504mobile element insertion1nstd215human GRCh38 chr2: 230,872,447-230,872,447 , GRCh37.p13 chr2: 231,737,162-231,737,162 ITM2C
    nsv6134538copy number variation1nstd213human GRCh37 chr2: 231,190,000-231,740,001 , GRCh38.p12 chr2: 230,325,285-230,875,286 SP100, HMGB1P3, 12 more genes
    nsv5960332insertion1nstd209human GRCh38 chr2: 230,872,430-230,872,430 , GRCh37.p13 chr2: 231,737,145-231,737,145 ITM2C
    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