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Items: 1 to 20 of 1755

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3138122copy number variation1nstd151human GRCh37 (hg19) chr5: 156,074,472-156,459,903 , GRCh38 (hg38) chr5: 156,647,462-157,032,892 SGCD, RNU6-556P, 5 more genes
    nsv3135982copy number variation1nstd151human GRCh37 (hg19) chr5: 156,074,472-156,353,328 , GRCh38 (hg38) chr5: 156,647,462-156,926,317 SGCD, PPP1R2B, 4 more genes
    nsv3132685copy number variation1nstd151human GRCh37 (hg19) chr5: 156,186,226-156,390,214 , GRCh38 (hg38) chr5: 156,759,215-156,963,203 SGCD, PPP1R2B, 3 more genes
    nsv3128992copy number variation1nstd151human GRCh37 (hg19) chr5: 156,074,472-156,375,515 , GRCh38 (hg38) chr5: 156,647,462-156,948,504 SGCD, PPP1R2B, 4 more genes
    nsv3128802copy number variation1nstd151human GRCh37 (hg19) chr5: 156,184,590-156,464,377 , GRCh38 (hg38) chr5: 156,757,579-157,037,366 SGCD, TIMD4, 4 more genes
    nsv3126367copy number variation1nstd151human GRCh37 (hg19) chr5: 156,016,239-156,376,747 , GRCh38 (hg38) chr5: 156,589,229-156,949,736 SGCD, LOC105377673, 4 more genes
    nsv3125512copy number variation1nstd151human GRCh37 (hg19) chr5: 156,021,940-156,349,232 , GRCh38 (hg38) chr5: 156,594,930-156,922,221 SGCD, TIMD4, 4 more genes
    nsv3123883copy number variation1nstd151human GRCh37 (hg19) chr5: 155,771,497-156,349,232 , GRCh38 (hg38) chr5: 156,344,487-156,922,221 SGCD, TIMD4, 4 more genes
    nsv3121530copy number variation1nstd151human GRCh37 (hg19) chr5: 156,016,239-156,186,404 , GRCh38 (hg38) chr5: 156,589,229-156,759,393 SGCD, LOC105377673
    nsv3120314copy number variation1nstd151human GRCh37 (hg19) chr5: 156,186,226-156,535,999 , GRCh38 (hg38) chr5: 156,759,215-157,108,988 SGCD, HAVCR2, 5 more genes
    nsv3118609copy number variation1nstd151human GRCh37 (hg19) chr5: 155,771,497-156,390,214 , GRCh38 (hg38) chr5: 156,344,487-156,963,203 SGCD, PPP1R2B, 4 more genes
    nsv3117622copy number variation1nstd145human GRCh37 (hg19) chr5: 155,876,180-155,879,921 , GRCh38 (hg38) chr5: 156,449,170-156,452,911 SGCD
    nsv3110940copy number variation5nstd145human GRCh37 (hg19) chr5: 155,311,642-155,312,412 , GRCh38 (hg38) chr5: 155,884,632-155,885,402 SGCD
    nsv3085068mobile element insertion1nstd144human GRCh37 (hg19) chr5: 155,619,886-155,619,886 , GRCh38 (hg38) chr5: 156,192,876-156,192,876 SGCD
    nsv3085067mobile element insertion1nstd144human GRCh37 (hg19) chr5: 155,616,634-155,616,634 , GRCh38 (hg38) chr5: 156,189,624-156,189,624 SGCD
    nsv3085066mobile element insertion1nstd144human GRCh37 (hg19) chr5: 155,370,366-155,370,366 , GRCh38 (hg38) chr5: 155,943,356-155,943,356 SGCD
    nsv3085065mobile element insertion1nstd144human GRCh37 (hg19) chr5: 155,339,876-155,339,876 , GRCh38 (hg38) chr5: 155,912,866-155,912,866 SGCD
    nsv3085064mobile element insertion1nstd144human GRCh37 (hg19) chr5: 155,242,034-155,242,034 , GRCh38 (hg38) chr5: 155,815,024-155,815,024 SGCD
    nsv3085063mobile element insertion1nstd144human GRCh37 (hg19) chr5: 155,120,044-155,120,044 , GRCh38 (hg38) chr5: 155,740,484-155,740,484 SGCD
    nsv3084897mobile element insertion1nstd144human GRCh37 (hg19) chr5: 155,976,161-155,976,161 , GRCh38 (hg38) chr5: 156,549,151-156,549,151 SGCD
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