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 160

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148243copy number variation1nstd102humanPathogenic GRCh38 chr7: 137,463,392-159,345,973 , GRCh37.p13 chr7: 137,148,138-159,128,663 MIR11400, TRBV24-1, 531 more genes
    nsv7148234copy number variation1nstd102humanLikely pathogenic GRCh38 chr7: 138,620,939-159,233,475 , GRCh37.p13 chr7: 138,305,684-159,026,165 AOC1, ALDH7A1P3, 515 more genes
    nsv7141732insertion1nstd232human GRCh37.p13 chr7: 142,989,560-142,989,560 , GRCh38.p12 chr7: 143,292,467-143,292,467 CASP2
    nsv7097864copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,781,014-150,301,047 , GRCh38.p12 chr7: 131,096,255-150,603,959 NOBOX, FAM131B, 466 more genes
    nsv7057176inversion1nstd229human GRCh38 chr7: 142,200,564-149,795,026 , GRCh37.p13 chr7: 141,988,816-149,492,114 RN7SL72P, RPL32P17, 258 more genes
    nsv7051735inversion1nstd229human GRCh38 chr7: 142,037,473-144,135,486 , GRCh37.p13 chr7: 141,988,816-143,832,579 LOC105375546, TRBV21-1, 162 more genes
    nsv7049746inversion1nstd229human GRCh38 chr7: 143,132,164-144,147,382 , GRCh37.p13 chr7: 142,829,257-143,844,475 RPL26P24, EPHA1, 55 more genes
    nsv6836967copy number variation1nstd229human GRCh38 chr7: 143,049,005-143,290,951 , GRCh37.p13 chr7: 142,746,106-142,988,044 RN7SL535P, TAS2R40, 9 more genes
    nsv6829218copy number variation1nstd229human GRCh38 chr7: 142,964,425-143,312,171 , GRCh37.p13 chr7: 142,661,512-143,009,264 OR6V1, HINT1P1, 14 more genes
    nsv6828881copy number variation1nstd229human GRCh38 chr7: 143,198,701-143,410,900 , GRCh37.p13 chr7: 142,895,794-143,107,993 EPHA1, FAM131B, 15 more genes
    nsv6828737copy number variation1nstd229human GRCh38 chr7: 143,289,552-143,298,744 , GRCh37.p13 chr7: 142,986,645-142,995,837 RN7SL481P, CASP2, 1 more genes
    nsv6825726copy number variation1nstd229human GRCh38 chr7: 143,291,701-143,439,700 , GRCh37.p13 chr7: 142,988,794-143,136,793 RN7SL481P, ZYX, 10 more genes
    nsv6636458copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,779,213-149,042,734 , GRCh38.p12 chr7: 132,094,454-149,345,643 TRBD2, TRBV5-2, 403 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313607copy number variation1nstd102humanUncertain significance GRCh37 chr7: 142,691,458-143,193,361 , GRCh38.p12 chr7: 142,994,373-143,496,268 FAM131B, TAS2R62P, 27 more genes
    nsv6291163copy number variation1nstd102humanPathogenic GRCh37 chr7: 133,851,002-159,119,707 , GRCh38.p12 chr7: 134,166,250-159,327,017 TRB, ZC3HAV1L, 579 more genes
    nsv6290262copy number variation1nstd102humanPathogenic GRCh37 chr7: 133,848,099-145,814,115 , GRCh38.p12 chr7: 134,163,347-146,117,023 TRBJ2-7, PRSS2, 341 more genes
    nsv6136967copy number variation1nstd213human GRCh37 chr7: 142,970,000-143,090,001 , GRCh38.p12 chr7: 143,272,907-143,392,908 FAM131B-AS2, MIR6892, 11 more genes
    nsv6135972copy number variation1nstd213human GRCh37 chr7: 142,120,000-143,090,001 , GRCh38.p12 chr7: 142,618,685-143,392,908 , GRCh38.p12 chr7|NT_187562.1: 622,348-1,111,570 , CASP2, 70 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