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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5907583copy number variation1nstd209human GRCh38 chr12: 33,416,073-33,416,131 , GRCh37.p13 chr12: 33,569,008-33,569,066 SYT10
    nsv5705322mobile element insertion1nstd211human GRCh38 chr12: 33,432,597-33,432,597 , GRCh37.p13 chr12: 33,585,532-33,585,532 SYT10
    nsv5589786copy number variation1nstd207human GRCh38 chr12: 33,416,072-33,416,129 , GRCh37.p13 chr12: 33,569,007-33,569,064 SYT10
    nsv5391484copy number variation1nstd186human GRCh37 chr12: 33,569,008-33,569,074 , GRCh38.p12 chr12: 33,416,073-33,416,139 SYT10
    nsv5379631translocation1nstd200human GRCh38 chr12: 33,391,785-33,391,785 , GRCh38 chr12: 33,615,540-33,615,540 , GRCh37.p13 chr12: 33,544,720-33,544,720 , GRCh37.p13 chr12: 33,768,475-33,768,475 SYT10
    nsv5355722translocation1nstd200human GRCh38 chr12: 33,416,073-33,416,073 , GRCh38 chr12: 33,416,139-33,416,139 , GRCh37.p13 chr12: 33,569,074-33,569,074 , GRCh37.p13 chr12: 33,569,008-33,569,008 SYT10
    nsv5034757inversion1nstd200human GRCh38 chr12: 33,114,818-33,535,749 , GRCh37.p13 chr12: 33,267,752-33,688,684 ST13P9, SYT10
    nsv4981975copy number variation1nstd200human GRCh38 chr12: 33,428,108-33,437,406 , GRCh37.p13 chr12: 33,581,043-33,590,341 SYT10
    nsv4981974copy number variation1nstd200human GRCh38 chr12: 33,414,930-33,418,482 , GRCh37.p13 chr12: 33,567,865-33,571,417 SYT10
    nsv4974525copy number variation1nstd200human GRCh38 chr12: 33,394,782-33,398,344 , GRCh37.p13 chr12: 33,547,717-33,551,279 SYT10
    nsv4974524copy number variation1nstd200human GRCh38 chr12: 33,350,987-33,421,609 , GRCh37.p13 chr12: 33,503,922-33,574,544 SYT10
    nsv4974521copy number variation1nstd200human GRCh38 chr12: 33,133,685-33,540,890 , GRCh37.p13 chr12: 33,286,619-33,693,825 ST13P9, SYT10
    nsv4846152copy number variation1nstd200human GRCh37 chr12: 33,522,317-34,808,705 , GRCh38.p12 chr12: 33,369,382-34,655,770 LOC105369726, RNU6-472P, 8 more genes
    nsv4840141copy number variation1nstd200human GRCh37 chr12: 33,569,008-33,569,074 , GRCh38.p12 chr12: 33,416,073-33,416,139 SYT10
    nsv4836808copy number variation1nstd200human GRCh37 chr12: 33,503,922-33,574,544 , GRCh38.p12 chr12: 33,350,987-33,421,609 SYT10
    nsv4831970copy number variation1nstd200human GRCh37 chr12: 33,562,384-33,562,943 , GRCh38.p12 chr12: 33,409,449-33,410,008 SYT10
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4685755copy number variation1nstd102humanUncertain significance GRCh37 chr12: 33,526,428-34,714,602 , GRCh38.p12 chr12: 33,373,493-34,561,667 AK6P1, RNU6-472P, 8 more genes
    nsv4681008copy number variation2nstd189human GRCh37.p13 chr12: 33,526,356-34,803,046 , GRCh38.p12 chr12: 33,373,421-34,650,111 ALG10, TUBB8P4, 8 more genes
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