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Items: 1 to 20 of 389

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148243copy number variation1nstd102humanPathogenic GRCh38 chr7: 137,463,392-159,345,973 , GRCh37.p13 chr7: 137,148,138-159,128,663 MIR11400, TRBV24-1, 531 more genes
    nsv7148234copy number variation1nstd102humanLikely pathogenic GRCh38 chr7: 138,620,939-159,233,475 , GRCh37.p13 chr7: 138,305,684-159,026,165 AOC1, ALDH7A1P3, 515 more genes
    nsv7147716insertion1nstd232human GRCh37.p13 chr7: 148,514,483-148,514,483 , GRCh38.p12 chr7: 148,817,391-148,817,391 EZH2
    nsv7139488copy number variation1nstd232human GRCh37.p13 chr7: 148,563,594-148,563,647 , GRCh38.p12 chr7: 148,866,502-148,866,555 EZH2
    nsv7139300insertion1nstd232human GRCh37.p13 chr7: 148,512,133-148,512,133 , GRCh38.p12 chr7: 148,815,041-148,815,041 EZH2
    nsv7138761insertion1nstd232human GRCh37.p13 chr7: 148,514,482-148,514,482 , GRCh38.p12 chr7: 148,817,390-148,817,390 EZH2
    nsv7097871copy number variation1nstd102humanUncertain significance GRCh37 chr7: 145,813,969-148,544,390 , GRCh38.p12 chr7: 146,116,877-148,847,298 LOC105375554, MIR548F4, 20 more genes
    nsv7097864copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,781,014-150,301,047 , GRCh38.p12 chr7: 131,096,255-150,603,959 NOBOX, FAM131B, 466 more genes
    nsv7097613copy number variation1nstd102humanUncertain significance GRCh37 chr7: 147,600,637-148,544,390 , GRCh38.p12 chr7: 147,903,545-148,847,298 LOC643438, RN7SL456P, 11 more genes
    nsv7097351copy number variation1nstd102humanUncertain significance GRCh37 chr7: 148,504,738-148,544,390 , GRCh38.p12 chr7: 148,807,646-148,847,298 EZH2, RNU7-20P
    nsv7097350copy number variation1nstd102humanPathogenic GRCh37 chr7: 146,471,343-148,544,390 , GRCh38.p12 chr7: 146,774,251-148,847,298 CNTNAP2, RNU7-20P, 19 more genes
    nsv7057176inversion1nstd229human GRCh38 chr7: 142,200,564-149,795,026 , GRCh37.p13 chr7: 141,988,816-149,492,114 RN7SL72P, RPL32P17, 258 more genes
    nsv7052478inversion1nstd229human GRCh38 chr7: 148,598,936-149,120,264 , GRCh37.p13 chr7: 148,296,028-148,817,356 RNY1, CUL1, 16 more genes
    nsv7050521inversion1nstd229human GRCh38 chr7: 148,854,357-148,855,300 , GRCh37.p13 chr7: 148,551,449-148,552,392 EZH2
    nsv7046837inversion1nstd229human GRCh38 chr7: 146,996,779-152,901,438 , GRCh37.p13 chr7: 146,693,871-152,598,523 RARRES2, RN7SL76P, 153 more genes
    nsv7040762inversion1nstd229human GRCh38 chr7: 148,598,948-149,120,315 , GRCh37.p13 chr7: 148,296,040-148,817,407 RNU6-650P, COX6B1P1, 16 more genes
    nsv6836887copy number variation1nstd229human GRCh38 chr7: 148,875,601-148,882,100 , GRCh37.p13 chr7: 148,572,693-148,579,192 EZH2
    nsv6833723copy number variation1nstd229human GRCh38 chr7: 148,875,546-148,882,145 , GRCh37.p13 chr7: 148,572,638-148,579,237 EZH2
    nsv6831539copy number variation1nstd229human GRCh38 chr7: 148,807,008-148,807,095 , GRCh37.p13 chr7: 148,504,100-148,504,187 EZH2
    nsv6826377copy number variation1nstd229human GRCh38 chr7: 148,854,493-148,855,389 , GRCh37.p13 chr7: 148,551,585-148,552,481 EZH2
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