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 103

    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
    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
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4733492copy number variation1nstd199human GRCh37 chr7: 112,621,241-113,138,777 , GRCh38.p12 chr7: 112,981,186-113,498,722 GPR85, SMIM30, 2 more genes
    nsv4676062copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 109,594,999-113,885,203 , GRCh38.p12 chr7: 109,954,942-114,245,148 IFRD1, PPP1R3A, 32 more genes
    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
    nsv4675322copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,617,406-123,217,914 , GRCh38.p12 chr7: 106,976,961-123,577,860 CBLL1-AS1, COMETT, 168 more genes
    nsv4455696copy number variation1nstd102humanUncertain significance GRCh37 chr7: 112,661,101-113,147,465 , GRCh38.p12 chr7: 113,021,046-113,507,410 LOC107986837, SMIM30, 1 more genes
    nsv4455557copy number variation1nstd102humanPathogenic GRCh37 chr7: 107,410,314-117,825,549 , GRCh38.p12 chr7: 107,769,869-118,185,495 RAC1P6, LOC101928012, 103 more genes
    nsv4455322copy number variation1nstd102humanUncertain significance GRCh37 chr7: 109,939,104-113,649,529 , GRCh38.p12 chr7: 110,299,047-114,009,474 LOC105375450, DOCK4, 28 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
    nsv4436502copy number variation1nstd102humanUncertain significance GRCh37 chr7: 111,303,881-114,362,948 , GRCh38.p12 chr7: 111,663,825-114,722,893 LOC101928012, RNA5SP238, 26 more genes
    nsv4371191copy number variation1nstd173human GRCh37 chr7: 108,606,430-119,657,890 , GRCh38.p12 chr7: 108,966,373-120,017,836 , LOC100421901, 94 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv3924380copy number variation1nstd102humanPathogenic GRCh37 chr7: 101,912,320-120,918,695 , GRCh38 chr7: 102,196,924-121,278,641 , NCBI36 chr7: 101,626,924-120,705,931 LOC102724434, LRRN3, 222 more genes
    nsv3923570copy number variation1nstd102humanPathogenic NCBI36 chr7: 107,583,881-122,963,817 , GRCh37.p13 chr7: 107,796,645-123,176,581 , GRCh38.p12 chr7: 108,156,200-123,536,527 ANKRD7, NDUFA5, 142 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
    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