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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112674copy number variation1nstd102humanPathogenic GRCh37 chr11: 111,957,571-111,966,518 , GRCh38.p12 chr11: 112,086,847-112,095,794 SDHD, TIMM8B
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5672624copy number variation1nstd102humanPathogenic GRCh37 chr11: 111,956,548-111,967,525 , GRCh38.p12 chr11: 112,085,824-112,096,801 SDHD, TIMM8B
    nsv5672550copy number variation1nstd102humanPathogenic GRCh37 chr11: 111,957,547-111,958,707 , GRCh38.p12 chr11: 112,086,823-112,087,983 SDHD, TIMM8B
    nsv5509179copy number variation1nstd206human GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687 , ATM, 153 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
    nsv5268729copy number variation1nstd204human GRCh38.p13 chr11: 112,092,519-112,094,823 , GRCh37.p13 chr11: 111,963,243-111,965,547 SDHD
    nsv4980686copy number variation1nstd200human GRCh38 chr11: 112,085,928-112,089,644 , GRCh37.p13 chr11: 111,956,652-111,960,368 TIMM8B, SDHD
    nsv4683939copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr11: 111,171,709-111,965,694 , GRCh38.p12 chr11: 111,300,984-112,094,970 FDXACB1, LOC107984386, 34 more genes
    nsv4683073copy number variation2nstd102humanUncertain significance GRCh37 chr11: 111,957,547-111,957,693 , GRCh38.p12 chr11: 112,086,823-112,086,969 TIMM8B, SDHD
    nsv4682890copy number variation2nstd102humanPathogenic GRCh37 chr11: 111,965,519-111,965,694 , GRCh38.p12 chr11: 112,094,795-112,094,970 SDHD
    nsv4681579copy number variation2nstd102humanUncertain significance GRCh37 chr11: 111,957,547-111,965,694 , GRCh38.p12 chr11: 112,086,823-112,094,970 SDHD, TIMM8B
    nsv4681419copy number variation1nstd102humanPathogenic GRCh37 chr11: 111,957,626-111,965,699 , GRCh38.p12 chr11: 112,086,902-112,094,975 SDHD, TIMM8B
    nsv4681078copy number variation2nstd102humanUncertain significance GRCh37 chr11: 111,958,526-111,965,694 , GRCh38.p12 chr11: 112,087,802-112,094,970 SDHD
    nsv4675680copy number variation1nstd102humanPathogenic GRCh37 chr11: 103,320,065-114,349,787 , GRCh38.p12 chr11: 103,449,337-114,479,065 DRD2, NCAM1, 181 more genes
    nsv4675323copy number variation1nstd102humanPathogenic GRCh37 chr11: 105,699,599-114,524,876 , GRCh38.p12 chr11: 105,828,873-114,654,154 RPSAP50, RNA5SP349, 155 more genes
    nsv4528491copy number variation1nstd166human GRCh37.p13 chr11: 111,895,464-112,013,887 , GRCh38.p12 chr11: 112,024,740-112,143,164 DLAT, IL18, 6 more genes
    nsv4506665mobile element insertion1nstd166human GRCh37.p13 chr11: 111,963,328-111,963,328 , GRCh38.p12 chr11: 112,092,604-112,092,604 SDHD
    nsv4456659copy number variation1nstd102humanUncertain significance GRCh37 chr11: 110,969,076-114,578,509 , GRCh38.p12 chr11: 111,098,352-114,707,787 RPS29P19, PPP2R1B, 95 more genes
    nsv4455554copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,101,411-116,680,918 , GRCh38.p12 chr11: 104,230,683-116,810,202 LINC02732, LINC02698, 198 more genes
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