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 307

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5439365copy number variation1nstd206human GRCh38 chr2: 240,579,810-240,582,295 , GRCh37.p13 chr2: 241,519,227-241,521,712 RNPEPL1, CAPN10-DT
    nsv5381323copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,201,756-243,048,760 , GRCh38.p12 chr2: 236,293,113-242,106,609 LRRFIP1, GPR35, 133 more genes
    nsv5203970copy number variation1nstd204human GRCh38.p13 chr2: 240,580,438-240,581,437 , GRCh37.p13 chr2: 241,519,855-241,520,854 CAPN10-DT, RNPEPL1
    nsv4914149copy number variation1nstd200human GRCh38 chr2: 240,522,069-240,756,640 , GRCh37.p13 chr2: 241,461,486-241,696,057 AQP12A, LOC100420500, 9 more genes
    nsv4768328copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,110,452-243,028,452 , GRCh38.p12 chr2: 232,245,742-242,086,301 LOC107985836, LOC105373980, 217 more genes
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4684239copy number variation1nstd102humanUncertain significance GRCh37 chr2: 238,863,455-243,048,760 , GRCh38.p12 chr2: 237,954,813-242,106,609 LOC285191, MTERF4, 103 more genes
    nsv4674624copy number variation1nstd102humanPathogenic GRCh37 chr2: 234,791,927-242,783,384 , GRCh38.p12 chr2: 233,883,281-241,841,232 LOC93463, DUSP28, 151 more genes
    nsv4674620copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,265,271-242,783,384 , GRCh38.p12 chr2: 236,356,628-241,841,232 OR6B2, COPS8, 122 more genes
    nsv4674409copy number variation1nstd102humanPathogenic GRCh37 chr2: 239,914,717-242,783,384 , GRCh38.p12 chr2: 238,993,021-241,841,232 GAL3ST2, UICLM, 68 more genes
    nsv4674036copy number variation1nstd102humanPathogenic GRCh37 chr2: 236,172,348-241,611,309 , GRCh38.p12 chr2: 235,263,704-240,671,892 ILKAP, MLPH, 95 more genes
    nsv4673913copy number variation1nstd102humanPathogenic GRCh37 chr2: 230,814,690-242,783,384 , GRCh38.p12 chr2: 229,949,974-241,841,232 MIR2467, D2HGDH, 270 more genes
    nsv4673906copy number variation1nstd102humanPathogenic GRCh37 chr2: 240,112,450-242,783,384 , GRCh38.p12 chr2: 239,190,754-241,841,232 HDLBP-AS1, MIR4786, 66 more genes
    nsv4583644copy number variation1nstd183human GRCh37 chr2: 241,450,639-241,527,840 , GRCh38.p12 chr2: 240,511,222-240,588,423 ANKMY1, CAPN10, 3 more genes
    nsv4578473copy number variation1nstd102humanUncertain significance GRCh37 chr2: 241,404,033-242,684,292 , GRCh38.p12 chr2: 240,464,616-241,744,877 SEPTIN2, CROCC2, 42 more genes
    nsv4436652copy number variation1nstd102humanPathogenic GRCh37 chr2: 239,894,072-243,048,760 , GRCh38.p12 chr2: 238,972,376-242,106,609 HDAC4-AS1, LOC105373971, 79 more genes
    nsv4386900copy number variation1nstd173human GRCh37 chr2: 237,508,557-242,783,396 , GRCh38.p12 chr2: 236,599,914-241,841,244 , LRRFIP1, 123 more genes
    nsv4347297copy number variation1nstd102humanPathogenic GRCh37 chr2: 239,071,623-243,048,760 , GRCh38.p12 chr2: 238,162,982-242,106,609 ANO7, LINC02610, 97 more genes
    nsv4347296copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 238,795,602-242,918,203 , GRCh38.p12 chr2: 237,886,960-241,976,052 AGXT, KIF1A, 101 more genes
    nsv4347295copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,028,693-242,708,080 , GRCh38.p12 chr2: 236,120,049-241,768,665 RBM44, LOC105373947, 123 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