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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093694copy number variation2nstd102humanUncertain significance GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878 VPS37C, POLR2G, 298 more genes
    nsv6915986copy number variation1nstd229human GRCh38 chr11: 64,935,377-65,143,014 , GRCh37.p13 chr11: 64,702,849-64,910,485 TM7SF2, HIGD1AP10, 19 more genes
    nsv6914187copy number variation1nstd229human GRCh38 chr11: 65,041,098-65,113,861 , GRCh37.p13 chr11: 64,808,570-64,881,333 TMEM262, TM7SF2, 5 more genes
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6903098copy number variation1nstd229human GRCh38 chr11: 65,043,415-65,050,165 , GRCh37.p13 chr11: 64,810,887-64,817,637 SAC3D1, NAALADL1
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 more genes
    nsv6475497copy number variation1nstd223human GRCh38 chr11: 65,042,382-65,050,077 , GRCh37.p13 chr11: 64,809,854-64,817,549 SAC3D1, NAALADL1
    nsv6470631copy number variation1nstd223human GRCh38 chr11: 64,935,377-65,143,014 , GRCh37.p13 chr11: 64,702,849-64,910,485 MAJIN, HIGD1AP10, 19 more genes
    nsv6458120copy number variation1nstd223human GRCh38 chr11: 65,040,220-65,093,556 , GRCh37.p13 chr11: 64,807,692-64,861,028 ZFPL1, NAALADL1, 5 more genes
    nsv6457728copy number variation1nstd223human GRCh38 chr11: 65,036,707-65,039,037 , GRCh37.p13 chr11: 64,804,179-64,806,509 SNX15, ARL2-SNX15, 1 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
    nsv6309121copy number variation2nstd102humanPathogenic GRCh37 chr11: 64,522,783-66,283,694 , GRCh38.p12 chr11: 64,755,311-66,516,223 SF3B2, ZNRD2-DT, 124 more genes
    nsv6132269copy number variation1nstd213human GRCh37 chr11: 64,390,000-65,950,001 , GRCh38.p12 chr11: 64,622,528-66,182,530 MRPL49, CTSW, 103 more genes
    nsv6132112copy number variation1nstd213human GRCh37 chr11: 64,220,000-68,010,001 , GRCh38.p12 chr11: 64,452,528-68,242,533 ACTN3, ALDH3B1, 212 more genes
    nsv5979747insertion1nstd209human GRCh37.p13 chr11: 64,806,501-64,806,501 , GRCh38 chr11: 65,039,029-65,039,029 SAC3D1, SNX15, 1 more genes
    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
    nsv5267852copy number variation1nstd204human GRCh38.p13 chr11: 64,173,401-65,676,300 , GRCh37.p13 chr11: 63,940,873-65,443,771 , TALAM1, 103 more genes
    nsv5139835mobile element insertion1nstd203human GRCh38 chr11: 65,039,034-65,039,048 , GRCh37.p13 chr11: 64,806,506-64,806,520 SAC3D1, SNX15, 1 more genes
    nsv5132238mobile element insertion1nstd203human GRCh38 chr11: 65,039,048-65,039,093 , GRCh37.p13 chr11: 64,806,520-64,806,565 SAC3D1, SNX15, 1 more genes
    nsv5124717mobile element insertion1nstd203human GRCh38 chr11: 65,039,029-65,039,048 , GRCh37.p13 chr11: 64,806,501-64,806,520 SAC3D1, SNX15, 1 more genes
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