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Items: 1 to 20 of 164

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962900insertion1nstd209human GRCh38 chr6: 89,099,413-89,099,413 , GRCh37.p13 chr6: 89,809,132-89,809,132 SRSF12, PM20D2
    nsv5639261insertion1nstd207human GRCh38 chr6: 89,099,413-89,099,413 , GRCh37.p13 chr6: 89,809,132-89,809,132 PM20D2, SRSF12
    nsv5223102copy number variation1nstd204human GRCh37.p13 chr6: 89,721,420-89,825,119 , GRCh38.p13 chr6: 89,011,701-89,115,400 PNRC1, PM20D2, 4 more genes
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4675039copy number variation1nstd102humanPathogenic GRCh37 chr6: 86,024,761-90,023,713 , GRCh38.p12 chr6: 85,315,043-89,313,994 C6orf163, LOC100652960, 65 more genes
    nsv4538272insertion1nstd166human GRCh37.p13 chr6: 89,809,117-89,809,117 , GRCh38.p12 chr6: 89,099,398-89,099,398 SRSF12, PM20D2
    nsv4456405copy number variation1nstd102humanUncertain significance GRCh37 chr6: 87,627,836-93,698,486 , GRCh38.p12 chr6: 86,918,118-92,988,768 MIR4643, LOC107986625, 82 more genes
    nsv4455227copy number variation1nstd102humanUncertain significance GRCh37 chr6: 88,783,642-96,282,103 , GRCh38.p12 chr6: 88,073,924-95,834,227 MDN1, DNAJC19P6, 65 more genes
    nsv4150435copy number variation1nstd166human GRCh37.p13 chr6: 89,813,282-89,813,391 , GRCh38.p12 chr6: 89,103,563-89,103,672 PM20D2, SRSF12
    nsv3957954copy number variation1nstd168human GRCh38 chr6: 89,086,631-89,145,100 , GRCh37.p13 chr6: 89,796,350-89,854,819 PM20D2, SRSF12, 2 more genes
    nsv3923528copy number variation1nstd102humanPathogenic NCBI36 chr6: 84,604,741-99,376,910 , GRCh38 chr6: 83,838,303-98,822,313 , GRCh37 chr6: 84,548,022-99,270,189 RNU4-72P, LOC100132830, 157 more genes
    nsv3922502copy number variation1nstd102humanUncertain significance NCBI36 chr6: 89,774,237-90,472,036 , GRCh37 chr6: 89,717,518-90,415,315 , GRCh38 chr6: 89,007,799-89,705,596 RN7SL11P, LOC105377889, 17 more genes
    nsv3921478copy number variation1nstd102humanPathogenic NCBI36 chr6: 76,692,636-93,477,232 , GRCh38 chr6: 75,926,199-92,710,793 , GRCh37 chr6: 76,635,916-93,420,511 SPACA1, TAF13P1, 187 more genes
    nsv3919111copy number variation1nstd102humanPathogenic GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637 RNU6-770P, MAP3K5-AS2, 810 more genes
    nsv3918084copy number variation1nstd102humanPathogenic GRCh37 chr6: 86,513,991-93,898,976 , GRCh38 chr6: 85,804,273-93,189,258 , NCBI36 chr6: 86,570,710-93,955,697 LOC105377897, GABRR2, 91 more genes
    nsv3914309copy number variation1nstd102humanPathogenic GRCh38 chr6: 82,569,098-93,753,476 , NCBI36 chr6: 83,335,534-94,519,915 , GRCh37 chr6: 83,278,815-94,463,194 ME1, GJB7, 136 more genes
    nsv3912992copy number variation1nstd102humanPathogenic GRCh38 chr6: 85,370,716-90,669,793 , NCBI36 chr6: 86,137,153-91,436,233 , GRCh37 chr6: 86,080,434-91,379,512 DNAJC19P6, RNU4-12P, 88 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
    nsv3885958copy number variation1nstd102humanUncertain significance GRCh37 chr6: 89,720,586-90,415,315 , GRCh38.p12 chr6: 89,010,867-89,705,596 PM20D2, LOC101929004, 17 more genes
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