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Items: 1 to 20 of 10231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3071867copy number variation1nstd45humanPathogenic NCBI36 (hg18) chr10: 81,673,628-88,733,220 , GRCh37 (hg19) chr10: 81,683,648-88,743,240 , GRCh38 (hg38) chr10: 79,923,892-86,983,483 HMGN2P8, BMS1P21, 39 more genes
    nsv3071859copy number variation1nstd45humanPathogenic NCBI36 (hg18) chr1: 61,315,534-61,701,048 , GRCh37 (hg19) chr1: 61,542,946-61,928,460 , GRCh38 (hg38) chr1: 61,077,274-61,462,788 NFIA, NFIA-AS1
    nsv3071203insertion1nstd90human GRCh37 (hg19) chr21: 42,009,063-42,009,063 , GRCh38 (hg38) chr21: 40,637,137-40,637,137 DSCAM
    nsv3070446copy number variation1nstd90human GRCh37 (hg19) chr21: 41,586,880-41,587,204 , GRCh38 (hg38) chr21: 40,214,953-40,215,277 DSCAM
    nsv3070390insertion1nstd90human GRCh37 (hg19) chr21: 46,894,710-46,894,711 , GRCh38 (hg38) chr21: 45,474,796-45,474,797 COL18A1
    nsv3068508insertion1nstd90human GRCh37 (hg19) chr6: 151,990,325-151,990,325 , GRCh38 (hg38) chr6: 151,669,190-151,669,190 ESR1
    nsv3067962insertion1nstd90human GRCh37 (hg19) chr21: 41,890,322-41,890,323 , GRCh38 (hg38) chr21: 40,518,395-40,518,396 DSCAM
    nsv3067558insertion1nstd90human GRCh37 (hg19) chr21: 41,586,865-41,586,865 , GRCh38 (hg38) chr21: 40,214,938-40,214,938 DSCAM
    nsv3067523copy number variation1nstd90human GRCh37 (hg19) chr6: 152,220,206-152,220,655 , GRCh38 (hg38) chr6: 151,899,071-151,899,520 ESR1
    nsv3067096copy number variation1nstd141human GRCh37 (hg19) chr21: 41,649,282-42,044,388 , GRCh38 (hg38) chr21: 40,277,355-40,672,462 DSCAM-AS1, DSCAM-IT1, 1 more genes
    nsv3067012copy number variation1nstd141human GRCh37 (hg19) chr21: 26,682,662-27,174,549 , GRCh38 (hg38) chr21: 25,310,348-25,802,238 MIR155HG, GABPA, 6 more genes
    nsv3066345insertion1nstd140human GRCh37 (hg19) chr21: 46,894,696-46,894,697 , GRCh38 (hg38) chr21: 45,474,782-45,474,783 COL18A1
    nsv3063234copy number variation1nstd140human GRCh38 (hg38) chr21: 40,682,639-40,682,762 , GRCh37 (hg19) chr21: 42,054,565-42,054,688 DSCAM
    nsv3062110insertion1nstd140human GRCh37 (hg19) chr21: 46,920,688-46,920,689 , GRCh38 (hg38) chr21: 45,500,774-45,500,775 COL18A1
    nsv3062109insertion1nstd140human GRCh37 (hg19) chr21: 46,919,495-46,919,496 , GRCh38 (hg38) chr21: 45,499,581-45,499,582 COL18A1
    nsv3060868insertion1nstd140human GRCh37 (hg19) chr21: 46,838,579-46,838,580 , GRCh38 (hg38) chr21: 45,418,664-45,418,665 COL18A1
    nsv3059969copy number variation1nstd140human GRCh37 (hg19) chr21: 41,957,250-41,957,369 , GRCh38 (hg38) chr21: 40,585,323-40,585,442 DSCAM
    nsv3058373insertion1nstd140human GRCh37 (hg19) chr21: 41,720,154-41,720,155 , GRCh38 (hg38) chr21: 40,348,227-40,348,228 DSCAM
    nsv3058372insertion1nstd140human GRCh37 (hg19) chr21: 41,452,064-41,452,065 , GRCh38 (hg38) chr21: 40,080,137-40,080,138 DSCAM
    nsv3058359insertion1nstd140human GRCh37 (hg19) chr21: 16,403,436-16,403,437 , GRCh38 (hg38) chr21: 15,031,115-15,031,116 NRIP1
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