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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3968901insertion1nstd168human GRCh38 (hg38) chr20: 36,951,460-36,985,229 , GRCh37.p13 chr20: 35,579,863-35,613,632 SAMHD1
    nsv3963573copy number variation1nstd168human GRCh38 (hg38) chr20: 36,901,153-36,912,217 , GRCh37.p13 chr20: 35,529,556-35,540,620 SAMHD1
    nsv3920218copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr20: 99,557-64,277,321 , GRCh37.p13 chr20: 80,198-62,908,674 , NCBI36 (hg18) chr20: 28,198-62,379,118 SAMHD1, ACTG1P3, 1352 more genes
    nsv3918053copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr20: 25,703,100-38,491,480 , GRCh37.p13 chr20: 25,755,100-39,058,066 , GRCh38.p12 chr20: 25,774,464-40,429,426 SAMHD1, AHCY, 304 more genes
    nsv3912723copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr20: 30,288,202-45,731,170 , GRCh37.p13 chr20: 30,824,541-46,297,763 , GRCh38.p12 chr20: 32,236,738-47,669,019 SAMHD1, ADA, 377 more genes
    nsv3910818copy number variation1nstd102humanUncertain significance NCBI36 (hg18) chr20: 25,616,026-62,435,964 , GRCh37.p13 chr20: 25,668,026-62,965,520 , GRCh38.p12 chr20: 25,687,390-64,334,167 SAMHD1, ATP5F1E, 876 more genes
    nsv3910142copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr20: 9,811,433-39,316,956 , GRCh37.p13 chr20: 9,792,081-37,945,599 , NCBI36 (hg18) chr20: 9,740,081-37,379,013 SAMHD1, ASIP, 572 more genes
    nsv3910049copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr20: 35,237,946-47,631,818 , GRCh37.p13 chr20: 33,825,749-46,260,562 , NCBI36 (hg18) chr20: 33,289,165-45,693,969 SAMHD1, EPB41L1, 296 more genes
    nsv3905072copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435 , NCBI36 (hg18) chr20: 11,244-62,419,232 SAMHD1, ADRA1D, 1356 more genes
    nsv3900559copy number variation1nstd102humanUncertain significance GRCh37 (hg19) chr20: 35,412,135-35,521,238 , GRCh38.p12 chr20: 36,783,732-36,892,835 , NCBI36 (hg18) chr20: 34,845,549-34,954,652 SAMHD1, SOGA1, 2 more genes
    nsv3898463copy number variation1nstd102humanBenign GRCh37 (hg19) chr20: 35,507,542-35,525,640 , GRCh38.p12 chr20: 36,879,139-36,897,237 , NCBI36 (hg18) chr20: 34,940,956-34,959,054 SAMHD1, TLDC2
    nsv3896520copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110 , NCBI36 (hg18) chr20: 11,244-62,382,907 SAMHD1, ACTG1P3, 1353 more genes
    nsv3895314copy number variation2nstd102humanPathogenic GRCh37 (hg19) chr20: 61,569-62,915,555 , GRCh38.p12 chr20: 80,928-64,284,202 , NCBI36 (hg18) chr20: 9,569-62,385,999 SAMHD1, JAG1, 1353 more genes
    nsv3892750copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941 , NCBI36 (hg18) chr20: 11,244-62,431,738 SAMHD1, ADA, 1357 more genes
    nsv3891215copy number variation1nstd102humanBenign GRCh37 (hg19) chr20: 35,523,179-35,525,640 , GRCh38.p12 chr20: 36,894,776-36,897,237 , NCBI36 (hg18) chr20: 34,956,593-34,959,054 SAMHD1
    nsv3888363copy number variation1nstd102humanUncertain significance GRCh38 (hg38) chr20: 36,904,137-36,912,572 , GRCh37.p13 chr20: 35,532,540-35,540,975 , NCBI36 (hg18) chr20: 34,965,954-34,974,389 SAMHD1
    nsv3887616copy number variation1nstd102humanUncertain significance GRCh38 (hg38) chr20: 36,897,807-36,897,818 , GRCh37.p13 chr20: 35,526,210-35,526,221 , NCBI36 (hg18) chr20: 34,959,624-34,959,635 SAMHD1
    nsv3883152copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr20: 36,948,745-36,957,728 , GRCh37.p13 chr20: 35,577,148-35,586,131 , NCBI36 (hg18) chr20: 35,010,562-35,019,545 SAMHD1
    nsv3883070copy number variation1nstd102humanLikely pathogenic GRCh38 (hg38) chr20: 36,911,198-36,919,539 , GRCh37.p13 chr20: 35,539,601-35,547,942 , NCBI36 (hg18) chr20: 34,973,015-34,981,356 SAMHD1
    nsv3877960copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr20: 36,898,545-36,951,644 , GRCh37.p13 chr20: 35,526,948-35,580,047 , NCBI36 (hg18) chr20: 34,960,362-35,013,461 SAMHD1
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