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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3968954copy number variation1nstd168human GRCh38 (hg38) chr6: 33,567,833-33,655,679 , GRCh37.p13 chr6: 33,535,610-33,623,456 ITPR3, GGNBP1, 4 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr6: 156,974-46,789,291 , GRCh37.p13 chr6: 156,974-46,757,028 , NCBI36 (hg18) chr6: 101,974-46,864,987 ITPR3, ACTG1P9, 1437 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 , NCBI36 (hg18) chr6: 110,632-170,761,395 ITPR3, ADGRB3, 3007 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 (hg19) chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 , NCBI36 (hg18) chr6: 101,975-170,761,407 ITPR3, BMP5, 3007 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 , NCBI36 (hg18) chr6: 53,666-170,822,096 ITPR3, ACTG1P9, 3014 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 , NCBI36 (hg18) chr6: 5,107-170,896,711 ITPR3, CRYBG1, 3018 more genes
    nsv3195088copy number variation9nstd152human GRCh38 (hg38) chr6: 33,677,893-33,692,208 , GRCh37.p13 chr6: 33,645,670-33,659,985 ITPR3
    nsv3190790copy number variation4nstd152human GRCh38 (hg38) chr6: 33,603,921-33,620,169 , GRCh37.p13 chr6: 33,571,698-33,587,946 ITPR3
    nsv3138253copy number variation1nstd151human GRCh37 (hg19) chr6: 33,659,389-33,690,969 , GRCh38.p12 chr6: 33,691,612-33,723,192 ITPR3, UQCC2, 2 more genes
    nsv3132307copy number variation1nstd151human GRCh37 (hg19) chr6: 33,608,258-33,630,456 , GRCh38.p12 chr6: 33,640,481-33,662,679 ITPR3
    nsv3129272copy number variation2nstd151human GRCh37 (hg19) chr6: 33,644,542-33,663,562 , GRCh38.p12 chr6: 33,676,765-33,695,785 ITPR3, UQCC2
    nsv3127422copy number variation1nstd151human GRCh37 (hg19) chr6: 33,608,258-33,608,336 , GRCh38.p12 chr6: 33,640,481-33,640,559 ITPR3
    nsv3127036copy number variation1nstd151human GRCh37 (hg19) chr6: 33,659,389-33,679,468 , GRCh38.p12 chr6: 33,691,612-33,711,691 ITPR3, UQCC2, 1 more genes
    nsv3125246copy number variation1nstd151human GRCh37 (hg19) chr6: 33,625,706-33,625,800 , GRCh38.p12 chr6: 33,657,929-33,658,023 ITPR3
    esv4010756copy number variation1estd233human GRCh37 (hg19) chr6: 32,496,000-38,995,000 , GRCh38.p12 chr6: 32,528,223-39,027,224 ITPR3, BAK1, 202 more genes
    nsv2779086copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 , NCBI36 (hg18) chr6: 101,975-170,761,407 ITPR3, LOC107986551, 3007 more genes
    esv3844338copy number variation1530estd219human GRCh37 (hg19) chr6: 33,582,080-33,586,984 , GRCh38.p12 chr6: 33,614,303-33,619,207 ITPR3
    esv3974576copy number variation7estd229human GRCh37 (hg19) chr6: 33,583,051-33,586,200 , GRCh38.p12 chr6: 33,615,274-33,618,423 ITPR3
    nsv2754530copy number variation1nstd130human GRCh37 (hg19) chr6: 33,581,702-33,608,379 , GRCh38.p12 chr6: 33,613,925-33,640,602 ITPR3, LOC101929188, 1 more genes
    nsv2456887short tandem repeat1nstd128human GRCh37 (hg19) chr6: 33,662,341-33,662,356 , GRCh38.p12 chr6: 33,694,564-33,694,579 ITPR3
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