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Items: 1 to 20 of 118

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    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
    nsv5477528copy number variation1nstd206human GRCh38 chr7: 55,282,120-56,410,000 , GRCh37.p13 chr7: 55,349,813-56,477,693 , MRPS17, 52 more genes
    nsv5229513copy number variation1nstd204human GRCh38.p13 chr7: 56,167,601-56,208,600 , GRCh37.p13 chr7: 56,235,294-56,276,293 LOC100130909
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4761040inversion1nstd199human GRCh37 chr7: 55,830,732-65,288,125 , GRCh38.p12 chr7: 55,763,039-65,823,138 , CCT6A, 247 more genes
    nsv4711364copy number variation1nstd195human GRCh37 chr7: 56,220,451-56,245,001 , GRCh38.p12 chr7: 56,152,758-56,177,308 IFITM3P4, LOC100130909
    nsv4616998copy number variation1nstd183human GRCh37 chr7: 56,155,561-56,330,552 , GRCh38.p12 chr7: 56,087,868-56,262,859 PHKG1, CHCHD2, 5 more genes
    nsv4612052copy number variation1nstd183human GRCh37 chr7: 56,155,087-56,326,872 , GRCh38.p12 chr7: 56,087,394-56,259,179 PHKG1, CHCHD2, 5 more genes
    nsv4611432copy number variation2nstd183human GRCh37 chr7: 55,619,800-56,385,412 , GRCh38.p12 chr7: 55,552,107-56,317,719 , LOC101928755, 37 more genes
    nsv4550512insertion1nstd166human GRCh37.p13 chr7: 56,244,307-56,244,307 , GRCh38.p12 chr7: 56,176,614-56,176,614 LOC100130909
    nsv4455806copy number variation1nstd102humanUncertain significance GRCh37 chr7: 52,809,787-58,025,873 , GRCh38.p12 chr7: 52,742,093-57,966,167 RPL31P35, SEC61G, 161 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
    nsv4400210copy number variation1nstd174human GRCh37 chr7: 55,619,800-56,483,244 , GRCh38.p12 chr7: 55,552,107-56,415,551 , PHKG1, 49 more genes
    nsv4394401copy number variation1nstd174human GRCh37 chr7: 56,117,100-56,632,479 , GRCh38.p12 chr7: 56,049,407-56,564,786 IFITM3P4, VN1R25P, 34 more genes
    nsv4394085copy number variation1nstd174human GRCh37 chr7: 55,731,868-56,494,502 , GRCh38.p12 chr7: 55,664,175-56,426,809 , LOC643348, 46 more genes
    nsv4385023copy number variation1nstd173human GRCh37 chr7: 56,189,913-56,330,507 , GRCh38.p12 chr7: 56,122,220-56,262,814 LOC105375288, LOC100130909, 2 more genes
    nsv4366528copy number variation1nstd173human GRCh37 chr7: 56,179,642-56,330,507 , GRCh38.p12 chr7: 56,111,949-56,262,814 IFITM3P4, NUPR2, 3 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
    nsv4147366copy number variation1nstd166human GRCh37.p13 chr7: 56,240,384-56,242,775 , GRCh38.p12 chr7: 56,172,691-56,175,082 LOC100130909
    nsv4137037copy number variation1nstd166human GRCh37.p13 chr7: 56,184,368-56,332,516 , GRCh38.p12 chr7: 56,116,675-56,264,823 LOC100130909, CCNJP1, 3 more genes
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