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Items: 1 to 20 of 95

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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
    nsv5478344copy number variation1nstd206human GRCh38 chr7: 56,342,453-56,635,465 , GRCh37.p13 chr7: 56,410,146-56,703,158 DKFZp434L192, LOC650226, 24 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
    nsv5225243copy number variation1nstd204human GRCh38.p13 chr7: 56,355,801-56,368,300 , GRCh37.p13 chr7: 56,423,494-56,435,993 CICP8, SEPTIN14P24, 1 more genes
    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
    nsv4612951copy number variation1nstd183human GRCh37 chr7: 56,419,329-56,445,602 , GRCh38.p12 chr7: 56,351,636-56,377,909 CICP8, LOC731631, 6 more genes
    nsv4609065copy number variation1nstd183human GRCh37 chr7: 56,382,055-56,612,161 , GRCh38.p12 chr7: 56,314,362-56,544,468 VN1R24P, LOC100419642, 19 more genes
    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
    nsv4411472copy number variation1nstd174human GRCh37 chr7: 56,419,329-56,445,602 , GRCh38.p12 chr7: 56,351,636-56,377,909 CICP8, LOC731631, 6 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
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv4150754copy number variation1nstd166human GRCh37.p13 chr7: 56,385,000-56,435,000 , GRCh38.p12 chr7: 56,317,307-56,367,307 CICP8, RNU6-1335P, 2 more genes
    nsv3922900copy number variation1nstd102humanUncertain significance GRCh37 chr7: 52,260,224-57,882,999 , NCBI36 chr7: 52,227,718-57,886,941 , GRCh38 chr7: 52,192,528-57,823,293 LOC102723656, LOC728376, 160 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
    nsv3917263copy number variation1nstd102humanPathogenic GRCh38 chr7: 33,328,312-62,377,476 , GRCh37 chr7: 33,367,924-61,831,899 , NCBI36 chr7: 33,334,449-61,469,334 MIR4649, LOC107986794, 444 more genes
    nsv3915342copy number variation1nstd102humanUncertain significance NCBI36 chr7: 52,149,644-57,498,383 , GRCh38 chr7: 52,114,454-57,434,735 , GRCh37 chr7: 52,182,150-57,493,216 VSTM2A, LOC101928401, 152 more genes
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