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 354

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148127copy number variation1nstd102humanUncertain significance GRCh37 chr7: 10,973,263-14,669,896 , GRCh38.p12 chr7: 10,933,636-14,630,271 LOC105375162, LOC105375156, 33 more genes
    nsv7054063inversion1nstd229human GRCh38 chr7: 7,723,636-12,911,662 , GRCh37.p13 chr7: 7,763,267-12,951,287 NXPH1, CCNB2P1, 50 more genes
    nsv7053494inversion1nstd229human GRCh38 chr7: 12,155,513-12,915,637 , GRCh37.p13 chr7: 12,195,139-12,955,262 SCIN, RN7SKP228, 13 more genes
    nsv7049984inversion1nstd229human GRCh38 chr7: 11,159,456-12,799,960 , GRCh37.p13 chr7: 11,199,083-12,839,585 THSD7A, LOC105375156, 17 more genes
    nsv7048158inversion1nstd229human GRCh38 chr7: 12,594,857-12,594,932 , GRCh37.p13 chr7: 12,634,482-12,634,557 LOC107986768, SCIN
    nsv7047916inversion1nstd229human GRCh38 chr7: 12,583,848-12,583,918 , GRCh37.p13 chr7: 12,623,473-12,623,543 SCIN
    nsv6817442copy number variation1nstd229human GRCh38 chr7: 12,619,710-12,671,058 , GRCh37.p13 chr7: 12,659,335-12,710,683 SCIN
    nsv6817204copy number variation1nstd229human GRCh38 chr7: 12,657,802-12,663,029 , GRCh37.p13 chr7: 12,697,427-12,702,654 SCIN
    nsv6817025copy number variation1nstd229human GRCh38 chr7: 12,640,193-12,662,973 , GRCh37.p13 chr7: 12,679,818-12,702,598 SCIN
    nsv6816537copy number variation1nstd229human GRCh38 chr7: 12,612,636-13,225,383 , GRCh37.p13 chr7: 12,652,261-13,265,008 ARL4A, LOC105375157, 5 more genes
    nsv6815603copy number variation1nstd229human GRCh38 chr7: 12,483,630-12,673,530 , GRCh37.p13 chr7: 12,523,256-12,713,155 TAS2R2P, LOC105375157, 4 more genes
    nsv6812832copy number variation1nstd229human GRCh38 chr7: 12,603,306-12,605,135 , GRCh37.p13 chr7: 12,642,931-12,644,760 SCIN
    nsv6810542copy number variation1nstd229human GRCh38 chr7: 12,596,360-12,596,416 , GRCh37.p13 chr7: 12,635,985-12,636,041 SCIN
    nsv6810364copy number variation1nstd229human GRCh38 chr7: 12,495,787-12,579,537 , GRCh37.p13 chr7: 12,535,413-12,619,162 LOC105375156, SCIN, 1 more genes
    nsv6809912copy number variation1nstd229human GRCh38 chr7: 12,570,696-12,572,753 , GRCh37.p13 chr7: 12,610,322-12,612,378 SCIN
    nsv6807803copy number variation1nstd229human GRCh38 chr7: 12,583,433-12,614,921 , GRCh37.p13 chr7: 12,623,058-12,654,546 LOC107986768, SCIN
    nsv6807195copy number variation1nstd229human GRCh38 chr7: 12,561,897-12,569,575 , GRCh37.p13 chr7: 12,601,523-12,609,201 SCIN
    nsv6805090copy number variation1nstd229human GRCh38 chr7: 11,673,765-12,709,856 , GRCh37.p13 chr7: 11,713,392-12,749,481 TAS2R2P, LOC105375155, 14 more genes
    nsv6804502copy number variation1nstd229human GRCh38 chr7: 12,657,801-12,663,000 , GRCh37.p13 chr7: 12,697,426-12,702,625 SCIN
    nsv6803877copy number variation1nstd229human GRCh38 chr7: 12,598,417-12,603,362 , GRCh37.p13 chr7: 12,638,042-12,642,987 SCIN
    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