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Items: 1 to 20 of 151

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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 , ACTB, 2676 more genes
    nsv5473800copy number variation1nstd206human GRCh38 chr7: 23,267,032-23,302,092 , GRCh37.p13 chr7: 23,306,651-23,341,711 GPNMB, MALSU1
    nsv5463796copy number variation1nstd206human GRCh38 chr7: 23,258,542-23,258,604 , GRCh37.p13 chr7: 23,298,161-23,298,223 GPNMB
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , GTF2IP7, 1832 more genes
    nsv4953496copy number variation1nstd200human GRCh38 chr7: 23,265,931-23,290,179 , GRCh37.p13 chr7: 23,305,550-23,329,798 GPNMB
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 LOC105375167, LOC105375144, 435 more genes
    nsv4828811copy number variation1nstd200human GRCh37 chr7: 23,305,550-23,329,798 , GRCh38.p12 chr7: 23,265,931-23,290,179 GPNMB
    nsv4828810copy number variation1nstd200human GRCh37 chr7: 23,257,505-23,367,536 , GRCh38.p12 chr7: 23,217,886-23,327,917 MALSU1, GPNMB, 2 more genes
    nsv4679102copy number variation1nstd189human GRCh37.p13 chr7: 23,083,268-24,187,619 , GRCh38.p12 chr7: 23,043,649-24,148,000 CLK2P1, GPNMB, 24 more genes
    nsv4616618copy number variation1nstd183human GRCh37 chr7: 23,145,295-23,311,044 , GRCh38.p12 chr7: 23,105,676-23,271,425 GPNMB, NUP42, 4 more genes
    nsv4555101insertion1nstd166human GRCh37.p13 chr7: 23,296,384-23,296,384 , GRCh38.p12 chr7: 23,256,765-23,256,765 GPNMB
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 LOC105375483, LOC100420549, 2771 more genes
    nsv4435897copy number variation1nstd102humanPathogenic GRCh37 chr7: 23,236,782-30,690,453 , GRCh38.p12 chr7: 23,197,163-30,650,837 LOC389473, LOC105375200, 143 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1581 more genes
    nsv3924159copy number variation1nstd102humanPathogenic NCBI36 chr7: 149,068-158,767,981 , GRCh38 chr7: 53,985-159,282,531 , GRCh37 chr7: 53,985-159,075,220 TRBJ1-2, LOC100134507, 2768 more genes
    nsv3922885copy number variation1nstd102humanPathogenic GRCh38 chr7: 20,561,456-32,005,143 , GRCh37 chr7: 20,601,079-32,044,755 , NCBI36 chr7: 20,567,604-32,011,280 HOXA10-AS, IL6-AS1, 203 more genes
    nsv3922329copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-27,236,023 , GRCh38 chr7: 43,360-27,196,404 , NCBI36 chr7: 138,443-27,202,548 CYTH3, LOC107986767, 428 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 TCAF1P1, LOC105375128, 2768 more genes
    nsv3918785copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-37,129,317 , NCBI36 chr7: 149,268-37,095,842 , GRCh38 chr7: 54,185-37,089,712 ZFAND2A, PRR15-DT, 576 more genes
    nsv3916683copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-26,867,253 , NCBI36 chr7: 149,268-26,833,778 , GRCh38 chr7: 54,185-26,827,634 ETV1, LOC107986770, 406 more genes
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