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 128

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5491761copy number variation1nstd206human GRCh38 chr7: 128,250,248-128,250,337 , GRCh37.p13 chr7: 127,890,301-127,890,390 LEP
    nsv5488525copy number variation1nstd206human GRCh38 chr7: 128,248,907-128,249,609 , GRCh37.p13 chr7: 127,888,960-127,889,662 LEP
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4958242copy number variation1nstd200human GRCh38 chr7: 128,247,703-128,251,444 , GRCh37.p13 chr7: 127,887,756-127,891,497 LEP
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4820497copy number variation1nstd200human GRCh37 chr7: 127,888,960-127,889,662 , GRCh38.p12 chr7: 128,248,907-128,249,609 LEP
    nsv4820496copy number variation1nstd200human GRCh37 chr7: 127,887,756-127,891,497 , GRCh38.p12 chr7: 128,247,703-128,251,444 LEP
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 RPL26P23, ST13P17, 887 more genes
    nsv4455826copy number variation1nstd102humanPathogenic GRCh37 chr7: 121,480,906-129,389,003 , GRCh38.p12 chr7: 121,840,852-129,749,163 ASB15, PNPT1P2, 127 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4381188copy number variation1nstd173human GRCh37 chr7: 127,846,898-127,889,168 , GRCh38.p12 chr7: 128,206,845-128,249,115 , LEP, 1 more genes
    nsv4322564inversion1nstd166human GRCh37.p13 chr7: 125,283,973-130,824,546 , GRCh38.p12 chr7: 125,643,919-131,139,787 , ARF5, 119 more genes
    nsv4163449copy number variation1nstd166human GRCh37.p13 chr7: 127,844,739-127,891,663 , GRCh38.p12 chr7: 128,204,686-128,251,610 , MIR129-1, 1 more genes
    nsv3923164copy number variation1nstd102humanPathogenic GRCh37 chr7: 121,658,176-128,547,780 , GRCh38 chr7: 122,018,122-128,907,727 , NCBI36 chr7: 121,445,412-128,335,016 GCC1, RNF133, 104 more genes
    nsv3922815copy number variation1nstd102humanPathogenic NCBI36 chr7: 96,887,100-158,409,214 , GRCh38 chr7: 97,419,852-158,923,762 , GRCh37 chr7: 97,049,164-158,716,453 SEPTIN7P6, MIR93, 1175 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 RNU6-438P, LOC105375300, 2682 more genes
    nsv3918979copy number variation1nstd102humanPathogenic GRCh37 chr7: 115,099,069-159,118,507 , NCBI36 chr7: 114,886,305-158,811,268 , GRCh38 chr7: 115,459,015-159,325,817 ABCF2, LOC105375581, 844 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