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 524

    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
    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
    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
    nsv6635562copy number variation1nstd227human GRCh37 chr7: 143,425,361-143,437,434 , GRCh38.p12 chr7: 143,728,268-143,740,341 , GRCh38.p12 chr7|NW_018654714.1: 272,587-284,661 TCAF2
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6631783copy number variation1nstd224human GRCh37 chr7: 143,426,263-143,874,190 , GRCh38.p12 chr7: 143,729,170-144,177,097 , GRCh38.p12 chr7|NW_018654714.1: 273,489-589,656 TCAF1, OR2F1, 25 more genes
    nsv6426680copy number variation1nstd223human GRCh38 chr7: 143,727,001-143,743,200 , GRCh37.p13 chr7: 143,424,094-143,440,293 TCAF2
    nsv6315434copy number variation1nstd102humanUncertain significance GRCh37 chr7: 143,425,718-144,075,390 , GRCh38.p12 chr7|NW_018654715.1: 1-409,704 , GRCh38.p12 chr7: 143,728,625-144,378,297 ARHGEF5, ARHGEF34P, 41 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 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
    nsv6142265copy number variation1nstd206human GRCh38 chr7: 143,722,000-143,727,700 , GRCh37.p13 chr7: 143,419,093-143,424,793 TCAF2
    nsv6141678copy number variation1nstd206human GRCh38 chr7: 143,522,800-143,650,300 , GRCh37.p13 chr7: 143,219,893-143,347,393 EPHA1-AS1, TCAF2, 7 more genes
    nsv6141635copy number variation1nstd206human GRCh38 chr7: 143,718,804-143,724,000 , GRCh37.p13 chr7: 143,415,897-143,421,093 TCAF2
    nsv6135900copy number variation1nstd213human GRCh37 chr7: 142,330,000-143,440,001 , GRCh38.p12 chr7: 142,622,486-143,742,908 , EPHA1, 82 more genes
    nsv6112163inversion1nstd212human GRCh37.p13 chr7: 143,397,898-143,515,508 , GRCh38 chr7: 143,700,805-143,818,415 LOC154761, TCAF2, 5 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