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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7062837inversion1nstd229human GRCh38 chr11: 40,841,838-44,720,409 , GRCh37.p13 chr11: 40,863,388-44,741,959 TTC17, ACCSL, 35 more genes
    nsv6909074copy number variation1nstd229human GRCh38 chr11: 43,710,266-43,953,276 , GRCh37.p13 chr11: 43,731,816-43,974,826 ALKBH3, RPL23AP63, 7 more genes
    nsv6906890copy number variation1nstd229human GRCh38 chr11: 43,890,530-43,915,807 , GRCh37.p13 chr11: 43,912,080-43,937,357 ALKBH3-AS1, SEC14L1P1, 1 more genes
    nsv6898115copy number variation1nstd229human GRCh38 chr11: 43,897,532-43,897,627 , GRCh37.p13 chr11: 43,919,082-43,919,177 SEC14L1P1, ALKBH3
    nsv6621096copy number variation1nstd224human GRCh37 chr11: 43,859,928-44,036,866 , GRCh38.p12 chr11: 43,838,378-44,015,316 HSD17B12, ALKBH3, 4 more genes
    nsv6466283copy number variation1nstd223human GRCh38 chr11: 43,710,265-43,953,275 , GRCh37.p13 chr11: 43,731,815-43,974,825 HSD17B12, ALKBH3, 7 more genes
    nsv6315539copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,769,957-44,952,669 , GRCh38.p12 chr11: 43,748,407-44,931,118 ACCS, ALKBH3-AS1, 16 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 TRR-TCT3-2, OR4A41P, 494 more genes
    nsv6315293copy number variation1nstd102humanUncertain significance GRCh38 chr11: 42,871,836-44,852,545 , GRCh37.p13 chr11: 42,893,386-44,874,096 ACCS, LINC02704, 26 more genes
    nsv6291196copy number variation1nstd102humanPathogenic GRCh37 chr11: 40,117,145-46,920,718 , GRCh38.p12 chr11: 40,095,595-46,899,167 LINC02687, ALKBH3, 86 more genes
    nsv5923003copy number variation1nstd209human GRCh38 chr11: 43,890,390-43,929,566 , GRCh37.p13 chr11: 43,911,940-43,951,116 SEC14L1P1, ALKBH3-AS1, 1 more genes
    nsv5864489copy number variation1nstd209human GRCh38 chr11: 43,890,335-43,901,681 , GRCh37.p13 chr11: 43,911,885-43,923,231 SEC14L1P1, ALKBH3
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv4987242copy number variation1nstd200human GRCh38 chr11: 43,710,265-43,953,275 , GRCh37.p13 chr11: 43,731,815-43,974,825 HSD17B12, ALKBH3, 7 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4729468copy number variation1nstd102humanUncertain significance GRCh37 chr11: 43,223,479-44,266,544 , GRCh38.p12 chr11: 43,201,929-44,244,994 MIR670, ALKBH3, 18 more genes
    nsv4710519copy number variation1nstd195human GRCh37 chr11: 43,800,201-44,412,451 , GRCh38.p12 chr11: 43,778,651-44,390,901 ACCSL, HSD17B12, 9 more genes
    nsv4675989copy number variation1nstd102humanUncertain significance GRCh37 chr11: 43,757,860-44,118,731 , GRCh38.p12 chr11: 43,736,310-44,097,181 SEC14L1P1, EXT2, 8 more genes
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