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Items: 1 to 20 of 260

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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
    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
    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
    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
    nsv6835475copy number variation1nstd229human GRCh38 chr7: 149,077,582-149,079,325 , GRCh37.p13 chr7: 148,774,674-148,776,417 ZNF786
    nsv6832993copy number variation1nstd229human GRCh38 chr7: 148,933,698-149,172,239 , GRCh37.p13 chr7: 148,630,790-148,869,331 ZNF398, RNU6-650P, 12 more genes
    nsv6829318copy number variation1nstd229human GRCh38 chr7: 149,089,153-149,097,899 , GRCh37.p13 chr7: 148,786,245-148,794,991 ZNF786
    nsv6825257copy number variation1nstd229human GRCh38 chr7: 149,064,672-149,086,398 , GRCh37.p13 chr7: 148,761,764-148,783,490 ZNF786
    nsv6820840copy number variation1nstd229human GRCh38 chr7: 149,068,612-149,078,408 , GRCh37.p13 chr7: 148,765,704-148,775,500 ZNF786
    nsv6636458copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,779,213-149,042,734 , GRCh38.p12 chr7: 132,094,454-149,345,643 TRBD2, TRBV5-2, 403 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6558115inversion1nstd223human GRCh38 chr7: 146,996,771-152,901,398 , GRCh37.p13 chr7: 146,693,863-152,598,483 ZNF398, PRKAG2-AS1, 153 more genes
    nsv6555642inversion1nstd223human GRCh38 chr7: 149,068,746-149,069,331 , GRCh37.p13 chr7: 148,765,838-148,766,423 ZNF786
    nsv6434368copy number variation1nstd223human GRCh38 chr7: 149,067,101-149,068,400 , GRCh37.p13 chr7: 148,764,193-148,765,492 ZNF786
    nsv6433409copy number variation1nstd223human GRCh38 chr7: 149,057,635-149,068,624 , GRCh37.p13 chr7: 148,754,727-148,765,716 ZNF786
    nsv6426172copy number variation1nstd223human GRCh38 chr7: 149,077,576-149,079,283 , GRCh37.p13 chr7: 148,774,668-148,776,375 ZNF786
    nsv6425334copy number variation1nstd223human GRCh38 chr7: 149,072,532-149,075,535 , GRCh37.p13 chr7: 148,769,624-148,772,627 ZNF786
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