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Items: 1 to 20 of 551

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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
    nsv7097607copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr7: 138,391,369-141,759,786 , GRCh38.p12 chr7: 138,706,624-142,059,986 LOC105375535, AGK-DT, 82 more genes
    nsv7047243inversion1nstd229human GRCh38 chr7: 140,412,248-142,426,166 , GRCh37.p13 chr7: 140,112,048-142,048,195 OR9A4, AGK-DT, 69 more genes
    nsv7044890inversion1nstd229human GRCh38 chr7: 140,412,271-142,426,160 , GRCh37.p13 chr7: 140,112,071-142,048,195 WEE2, LOC105375535, 69 more genes
    nsv7040689inversion1nstd229human GRCh38 chr7: 140,412,886-142,426,274 , GRCh37.p13 chr7: 140,112,686-142,048,195 MYL6P4, TMEM178B, 69 more genes
    nsv6837091copy number variation1nstd229human GRCh38 chr7: 140,528,940-140,531,643 , GRCh37.p13 chr7: 140,228,740-140,231,443 DENND2A
    nsv6835135copy number variation1nstd229human GRCh38 chr7: 140,625,220-140,625,394 , GRCh37.p13 chr7: 140,325,020-140,325,194 DENND2A
    nsv6834293copy number variation1nstd229human GRCh38 chr7: 140,610,622-140,615,186 , GRCh37.p13 chr7: 140,310,422-140,314,986 DENND2A
    nsv6833030copy number variation1nstd229human GRCh38 chr7: 140,603,111-140,617,464 , GRCh37.p13 chr7: 140,302,911-140,317,264 DENND2A
    nsv6832379copy number variation1nstd229human GRCh38 chr7: 140,537,119-140,543,320 , GRCh37.p13 chr7: 140,236,919-140,243,120 DENND2A
    nsv6830560copy number variation1nstd229human GRCh38 chr7: 140,551,199-140,659,337 , GRCh37.p13 chr7: 140,250,999-140,359,137 LOC105375535, DENND2A, 1 more genes
    nsv6829978copy number variation1nstd229human GRCh38 chr7: 140,016,565-141,119,379 , GRCh37.p13 chr7: 139,716,365-140,819,179 KDM7A, LOC107986854, 29 more genes
    nsv6828540copy number variation1nstd229human GRCh38 chr7: 140,602,501-140,618,900 , GRCh37.p13 chr7: 140,302,301-140,318,700 DENND2A
    nsv6828085copy number variation1nstd229human GRCh38 chr7: 140,583,302-140,584,128 , GRCh37.p13 chr7: 140,283,102-140,283,928 DENND2A
    nsv6827773copy number variation1nstd229human GRCh38 chr7: 140,512,422-140,525,599 , GRCh37.p13 chr7: 140,212,222-140,225,399 DENND2A
    nsv6826079copy number variation1nstd229human GRCh38 chr7: 140,592,458-140,595,003 , GRCh37.p13 chr7: 140,292,258-140,294,803 DENND2A
    nsv6823585copy number variation1nstd229human GRCh38 chr7: 140,535,620-140,543,079 , GRCh37.p13 chr7: 140,235,420-140,242,879 DENND2A
    nsv6822943copy number variation1nstd229human GRCh38 chr7: 140,523,854-140,525,105 , GRCh37.p13 chr7: 140,223,654-140,224,905 DENND2A
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