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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5559488sequence alteration1nstd206human GRCh37.p13 chr3: 194,362,410-194,675,824 , GRCh38 chr3: 194,641,681-194,955,095 , LSG1, 6 more genes
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5449508copy number variation1nstd206human GRCh38 chr3: 194,433,000-194,791,574 , GRCh37.p13 chr3: 194,153,729-194,512,303 RNU6-1101P, FAM151AP1, 11 more genes
    nsv4925029copy number variation1nstd200human GRCh38 chr3: 194,688,539-194,697,926 , GRCh37.p13 chr3: 194,409,268-194,418,655 FAM43A
    nsv4685587copy number variation1nstd102humannot provided GRCh37 chr3: 194,161,542-194,998,084 , GRCh38.p12 chr3: 194,440,813-195,277,355 RPL23AP93, LSG1, 22 more genes
    nsv4596324copy number variation1nstd183human GRCh37 chr3: 193,962,049-194,571,078 , GRCh38.p12 chr3: 194,244,260-194,850,349 , LINC01968, 20 more genes
    nsv4470832mobile element insertion1nstd166human GRCh37.p13 chr3: 194,406,485-194,406,485 , GRCh38.p12 chr3: 194,685,756-194,685,756 FAM43A
    nsv4451465copy number variation1nstd102humanUncertain significance GRCh37 chr3: 194,363,991-194,497,236 , GRCh38.p12 chr3: 194,643,262-194,776,507 LOC105374292, LSG1, 4 more genes
    nsv4436392copy number variation1nstd102humanPathogenic GRCh37 chr3: 188,386,566-197,838,262 , GRCh38.p12 chr3: 188,668,778-198,111,391 PPP1R2, GCNT1P3, 194 more genes
    nsv4399690copy number variation1nstd174human GRCh37 chr3: 194,391,980-194,440,186 , GRCh38.p12 chr3: 194,671,251-194,719,457 LSG1, FAM43A, 2 more genes
    nsv4385260copy number variation2nstd173human GRCh37 chr3: 194,394,289-194,438,291 , GRCh38.p12 chr3: 194,673,560-194,717,562 LOC105374292, LINC01968, 1 more genes
    nsv4379440copy number variation1nstd173human GRCh37 chr3: 194,394,289-194,442,372 , GRCh38.p12 chr3: 194,673,560-194,721,643 LINC01968, FAM43A, 1 more genes
    nsv4095739copy number variation1nstd166human GRCh37.p13 chr3: 194,409,268-194,418,653 , GRCh38.p12 chr3: 194,688,539-194,697,924 FAM43A
    nsv4093801copy number variation1nstd166human GRCh37.p13 chr3: 194,334,605-194,716,963 , GRCh38.p12 chr3: 194,613,876-194,996,234 , LOC105374294, 8 more genes
    nsv3967064copy number variation1nstd168human GRCh38 chr3: 194,622,325-194,700,426 , GRCh37.p13 chr3: 194,343,054-194,421,155 FAM43A, TMEM44, 1 more genes
    nsv3924766copy number variation1nstd102humanPathogenic GRCh38 chr3: 194,424,496-198,168,758 , NCBI36 chr3: 195,626,514-199,380,026 , GRCh37 chr3: 194,145,225-197,895,629 XXYLT1, PIGZ, 119 more genes
    nsv3924195copy number variation1nstd102humanPathogenic GRCh38 chr3: 193,704,605-198,125,115 , NCBI36 chr3: 194,905,088-199,336,383 , GRCh37 chr3: 193,422,394-197,851,986 LOC105374298, LINC01983, 139 more genes
    nsv3922385copy number variation1nstd102humanPathogenic NCBI36 chr3: 177,369,007-199,329,651 , GRCh37 chr3: 175,886,313-197,845,254 , GRCh38 chr3: 176,168,525-198,118,383 LINC02053, RTP4, 414 more genes
    nsv3921532copy number variation1nstd102humanPathogenic GRCh38 chr3: 190,667,663-198,110,178 , NCBI36 chr3: 191,868,146-199,321,446 , GRCh37 chr3: 190,385,452-197,837,049 LOC105374282, PIGX, 173 more genes
    nsv3920718copy number variation1nstd102humanPathogenic NCBI36 chr3: 188,646,713-196,231,151 , GRCh37 chr3: 187,164,019-194,749,862 , GRCh38 chr3: 187,446,231-195,029,133 LOC105374283, MIR944, 105 more genes
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