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Items: 1 to 20 of 483

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141739insertion1nstd232human GRCh37.p13 chrX: 19,092,459-19,092,459 , GRCh38.p12 chrX: 19,074,341-19,074,341 ADGRG2, LOC101928415
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098361copy number variation1nstd102humanUncertain significance GRCh37 chrX: 18,664,107-19,032,212 , GRCh38.p12 chrX: 18,645,987-19,014,094 PPEF1, RN7SL48P, 10 more genes
    nsv7098359copy number variation1nstd102humanUncertain significance GRCh37 chrX: 18,525,053-20,284,750 , GRCh38.p12 chrX: 18,506,933-20,266,632 PPEF1, PDHA1, 23 more genes
    nsv7098010copy number variation1nstd102humanUncertain significance GRCh37 chrX: 18,593,454-19,086,952 , GRCh38.p12 chrX: 18,575,334-19,068,834 HAUS1P2, CDKL5, 10 more genes
    nsv7086039copy number variation1nstd229human GRCh38 chrX: 19,083,325-19,364,799 , GRCh37.p13 chrX: 19,101,443-19,382,917 PDHA1, MAP3K15, 2 more genes
    nsv7086038copy number variation1nstd229human GRCh38 chrX: 19,080,755-19,083,064 , GRCh37.p13 chrX: 19,098,873-19,101,182 LOC101928415, ADGRG2
    nsv7086037copy number variation1nstd229human GRCh38 chrX: 19,079,541-19,081,541 , GRCh37.p13 chrX: 19,097,659-19,099,659 LOC101928415, ADGRG2
    nsv7086036copy number variation1nstd229human GRCh38 chrX: 19,074,341-19,074,395 , GRCh37.p13 chrX: 19,092,459-19,092,513 ADGRG2, LOC101928415
    nsv7086035copy number variation1nstd229human GRCh38 chrX: 19,063,679-19,756,609 , GRCh37.p13 chrX: 19,081,797-19,774,727 MAP3K15, SH3KBP1, 4 more genes
    nsv7086034copy number variation1nstd229human GRCh38 chrX: 19,060,798-19,067,526 , GRCh37.p13 chrX: 19,078,916-19,085,644 ADGRG2, LOC101928415
    nsv7086033copy number variation1nstd229human GRCh38 chrX: 19,058,846-19,652,091 , GRCh37.p13 chrX: 19,076,964-19,670,209 SH3KBP1, EIF5P2, 4 more genes
    nsv7086032copy number variation1nstd229human GRCh38 chrX: 19,052,711-19,052,923 , GRCh37.p13 chrX: 19,070,829-19,071,041 LOC101928415, ADGRG2
    nsv7086031copy number variation1nstd229human GRCh38 chrX: 19,046,601-19,072,800 , GRCh37.p13 chrX: 19,064,719-19,090,918 ADGRG2, LOC101928415
    nsv7086030copy number variation1nstd229human GRCh38 chrX: 19,045,310-19,048,246 , GRCh37.p13 chrX: 19,063,428-19,066,364 ADGRG2, LOC101928415
    nsv7086029copy number variation1nstd229human GRCh38 chrX: 19,015,412-19,026,986 , GRCh37.p13 chrX: 19,033,530-19,045,104 ADGRG2, LOC101928415
    nsv7086028copy number variation1nstd229human GRCh38 chrX: 19,009,278-19,009,426 , GRCh37.p13 chrX: 19,027,396-19,027,544 ADGRG2, LOC101928415
    nsv7086027copy number variation1nstd229human GRCh38 chrX: 18,993,668-18,994,392 , GRCh37.p13 chrX: 19,011,786-19,012,510 ADGRG2, LOC101928415
    nsv7086025copy number variation1nstd229human GRCh38 chrX: 18,966,905-18,987,446 , GRCh37.p13 chrX: 18,985,023-19,005,564 PHKA2, LOC101928415, 1 more genes
    nsv7086020copy number variation1nstd229human GRCh38 chrX: 18,946,787-19,381,311 , GRCh37.p13 chrX: 18,964,905-19,399,429 PDHA1, MAP3K15, 3 more genes
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