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 216

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055819inversion1nstd229human GRCh37.p13 chr7|NW_003571037.1: 152,792-312,266 , GRCh38 chr7: 102,228,462-102,387,936 , GRCh37.p13 chr7: 101,871,742-102,028,383 LOC100289561, SH2B2, 6 more genes
    nsv7055390inversion1nstd229human GRCh38 chr7: 100,184,977-102,400,588 , GRCh37.p13 chr7: 99,782,600-101,718,950 SLC12A9-AS1, STAG3, 84 more genes
    nsv7052662inversion1nstd229human GRCh38 chr7: 102,309,147-103,483,817 , GRCh37.p13 chr7: 102,072,448-103,124,264 S100A11P1, RPL7AP39, 46 more genes
    nsv7040420inversion1nstd229human GRCh38 chr7: 101,445,712-104,173,878 , GRCh37.p13 chr7: 101,088,993-103,814,326 ALKBH4, RPS29P16, 54 more genes
    nsv6818476copy number variation1nstd229human GRCh38 chr7: 102,321,437-102,410,929 , GRCh37.p13 chr7|NW_003571037.1: 245,767-335,259 , GRCh37.p13 chr7: 101,961,904-102,051,376 SH2B2, SPDYE6, 7 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
    nsv6631801copy number variation1nstd224human GRCh37 chr7: 101,957,816-102,114,090 , GRCh38.p12 chr7: 102,317,349-102,473,643 ALKBH4, LOC100630923, 13 more genes
    nsv6631293copy number variation1nstd224human GRCh37 chr7: 101,870,948-102,113,373 , GRCh38.p12 chr7: 102,227,668-102,472,926 CUX1, ALKBH4, 15 more genes
    nsv6617867copy number variation1nstd223human GRCh38 chr7: 102,327,148-102,380,454 , GRCh37.p13 chr7: 101,967,566-102,020,901 , GRCh37.p13 chr7|NW_003571037.1: 251,478-304,784 LOC107986717, SPDYE6, 3 more genes
    nsv6602521copy number variation1nstd223human GRCh38 chr7: 102,167,380-103,063,308 , GRCh37.p13 chr7: 102,072,448-102,703,755 MIR4467, MIR548O, 32 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313576copy number variation1nstd102humanPathogenic GRCh37 chr7: 100,676,872-119,156,160 , GRCh38.p12 chr7: 101,033,591-119,516,106 LHFPL3-AS2, CTB-30L5.1, 233 more genes
    nsv6313503copy number variation1nstd102humanPathogenic GRCh37 chr7: 99,417,471-111,586,308 , GRCh38.p12 chr7: 99,819,848-111,946,253 GJC3, LAMB4, 237 more genes
    nsv6291301copy number variation1nstd102humanUncertain significance GRCh37 chr7: 101,729,998-102,114,340 , GRCh38.p12 chr7: 102,086,718-102,473,893 LOC105375433, CUX1, 15 more genes
    nsv6181462copy number variation1nstd214human GRCh38 chr7: 102,348,399-102,348,473 , GRCh37.p13 chr7: 101,988,839-101,988,913 , GRCh37.p13 chr7|NW_003571037.1: 272,729-272,803 SPDYE6
    nsv6141707copy number variation1nstd206human GRCh37.p13 chr7|NW_003571037.1: 253,109-307,109 , GRCh38 chr7: 102,328,779-102,382,779 , GRCh37.p13 chr7: 101,969,196-102,023,226 PMS2P12, LOC100289561, 3 more genes
    nsv6136532copy number variation1nstd213human GRCh37 chr7: 101,870,000-102,140,001 , GRCh38.p12 chr7: 102,226,720-102,499,554 LRWD1, LOC100289561, 16 more genes
    nsv6136217copy number variation1nstd213human GRCh37 chr7: 99,390,000-104,070,001 , GRCh38.p12 chr7: 99,792,377-104,429,553 AZGP1, CRYZP1, 157 more genes
    nsv6115483copy number variation1nstd186human GRCh37 chr7: 101,988,219-101,999,227 , GRCh38.p12 chr7: 102,347,779-102,358,779 SPDYE6
    nsv6107847inversion1nstd212human GRCh38 chr7: 100,184,978-102,378,892 , GRCh37.p13 chr7: 99,782,601-101,718,950 , ACHE, 87 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