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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
    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
    nsv4715888copy number variation1nstd195human GRCh37 chr7: 102,923,401-103,024,201 , GRCh38.p12 chr7: 103,282,954-103,383,754 PSMC2, PMPCB, 3 more genes
    nsv4679959copy number variation1nstd189human GRCh37.p13 chr7: 102,979,862-103,356,556 , GRCh38.p12 chr7: 103,339,415-103,716,109 RELN, PSMC2, 6 more genes
    nsv4455210copy number variation1nstd102humanUncertain significance GRCh37 chr7: 102,333,119-103,158,261 , GRCh38.p12 chr7: 102,692,672-103,517,814 S100A11P1, RN7SKP198, 23 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
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv3956357copy number variation1nstd168human GRCh38 chr7: 103,227,201-103,342,954 , GRCh37.p13 chr7: 102,867,648-102,983,401 PSMC2, PMPCB, 3 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
    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
    nsv3921180copy number variation1nstd102humanLikely benign GRCh37 chr7: 102,332,827-102,991,361 , NCBI36 chr7: 102,120,063-102,778,597 , GRCh38 chr7: 102,692,380-103,350,914 RN7SKP198, SLC26A5, 20 more genes
    nsv3920103copy number variation1nstd102humanPathogenic NCBI36 chr7: 100,955,796-104,860,145 , GRCh38 chr7: 101,525,795-105,432,462 , GRCh37 chr7: 101,169,076-105,072,909 RNU6-1322P, PRKRIP1, 66 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
    nsv3918078copy number variation1nstd102humanPathogenic NCBI36 chr7: 102,235,882-105,128,791 , GRCh37 chr7: 102,448,646-105,341,555 , GRCh38 chr7: 102,808,199-105,701,108 LHFPL3, NAPEPLD, 40 more genes
    nsv3912608copy number variation1nstd102humanUncertain significance NCBI36 chr7: 102,754,386-103,190,858 , GRCh37 chr7: 102,967,150-103,403,622 , GRCh38 chr7: 103,326,703-103,763,175 RELN, PSMC2, 7 more genes
    nsv3912378copy number variation1nstd102humanPathogenic GRCh38 chr7: 101,807,149-112,414,850 , GRCh37 chr7: 101,450,429-112,054,905 , NCBI36 chr7: 101,237,149-111,842,141 DNAJC2, LOC100420226, 139 more genes
    nsv3909087copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620 MNX1-AS2, VN1R31P, 2682 more genes
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