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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6825744copy number variation1nstd229human GRCh38 chr7: 120,119,180-121,466,883 , GRCh37.p13 chr7: 119,759,234-121,106,937 WNT16, CYCSP19, 12 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
    nsv6606071copy number variation1nstd223human GRCh38 chr7: 120,964,710-120,965,326 , GRCh37.p13 chr7: 120,604,764-120,605,380 ING3
    nsv6605609copy number variation1nstd223human GRCh38 chr7: 120,961,758-120,962,320 , GRCh37.p13 chr7: 120,601,812-120,602,374 ING3
    nsv6569428inversion1nstd223human GRCh38 chr7: 120,954,190-120,955,381 , GRCh37.p13 chr7: 120,594,244-120,595,435 ING3
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6314995copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 114,885,745-124,728,629 , GRCh38.p12 chr7: 115,245,691-125,088,575 CAPZA2, CAV1, 109 more genes
    nsv6313851copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,984,287-128,949,489 , GRCh38.p12 chr7: 107,343,842-129,309,648 DOCK4-AS1, RPL3P8, 262 more genes
    nsv6313819copy number variation1nstd102humanUncertain significance GRCh37 chr7: 120,268,066-120,869,197 , GRCh38.p12 chr7: 120,628,012-121,229,143 RNU6-581P, TSPAN12, 7 more genes
    nsv6239644mobile element insertion1nstd215human GRCh38 chr7: 120,958,542-120,958,542 , GRCh37.p13 chr7: 120,598,596-120,598,596 ING3
    nsv6136546copy number variation1nstd213human GRCh37 chr7: 120,110,000-126,120,001 , GRCh38.p12 chr7: 120,469,946-126,479,947 SSU72L6, IQUB, 67 more genes
    nsv6136545copy number variation1nstd213human GRCh37 chr7: 119,960,000-120,760,001 , GRCh38.p12 chr7: 120,319,946-121,119,947 KCND2, TSPAN12, 6 more genes
    nsv6135880copy number variation1nstd213human GRCh37 chr7: 119,540,000-121,050,001 , GRCh38.p12 chr7: 119,899,946-121,409,947 KCND2, FAM3C, 13 more genes
    nsv6135872copy number variation1nstd213human GRCh37 chr7: 113,230,000-128,010,001 , GRCh38.p12 chr7: 113,589,945-128,369,947 CAV1, SLC13A1, 154 more genes
    nsv6135548copy number variation1nstd213human GRCh37 chr7: 119,550,000-120,950,001 , GRCh38.p12 chr7: 119,909,946-121,309,947 ING3, RNA5SP241, 9 more genes
    nsv6135545copy number variation1nstd213human GRCh37 chr7: 117,870,000-125,940,001 , GRCh38.p12 chr7: 118,229,946-126,299,947 GPR37, KCND2, 78 more genes
    nsv5912833copy number variation1nstd209human GRCh38 chr7: 120,960,390-120,960,540 , GRCh37.p13 chr7: 120,600,444-120,600,594 ING3
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5381759copy number variation1nstd102humanPathogenic GRCh37 chr7: 116,297,277-126,370,694 , GRCh38.p12 chr7: 116,657,223-126,730,640 TMEM229A, ST7-OT3, 110 more genes
    nsv5371113translocation1nstd200human GRCh38 chr7: 121,176,483-121,176,483 , GRCh38 chr7: 120,965,621-120,965,621 , GRCh37.p13 chr7: 120,605,675-120,605,675 , GRCh37.p13 chr7: 120,816,537-120,816,537 ING3, CPED1
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