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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3132419copy number variation1nstd151human GRCh37 (hg19) chr2: 198,299,693-198,511,395 , GRCh38 (hg38) chr2: 197,434,969-197,646,671 SF3B1, HSPD1, 8 more genes
    nsv3119338copy number variation1nstd151human GRCh37 (hg19) chr2: 197,860,096-198,437,009 , GRCh38 (hg38) chr2: 196,995,372-197,572,285 SF3B1, HSPE1, 17 more genes
    nsv3110051copy number variation1nstd37humanLikely pathogenic NCBI36 (hg18) chr2: 195,941,520-200,787,299 , GRCh37 (hg19) chr2: 196,233,275-201,079,054 , GRCh38 (hg38) chr2: 195,368,551-200,214,331 SF3B1, SATB2, 62 more genes
    esv4010563copy number variation1estd233human GRCh37 (hg19) chr2: 194,751,000-199,172,000 , GRCh38 (hg38) chr2: 193,886,276-198,307,276 SF3B1, HSPD1, 54 more genes
    nsv2787496copy number variation1nstd132human NCBI36 (hg18) chr2: 197,971,391-198,489,105 , GRCh37 (hg19) chr2: 198,263,146-198,780,860 , GRCh38 (hg38) chr2: 197,398,422-197,916,136 SF3B1, BOLL, 12 more genes
    nsv2779041copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chr2: 110,190,938-242,751,149 , GRCh37 (hg19) chr2: 110,833,649-243,102,476 , GRCh38 (hg38) chr2: 110,076,072-242,157,305 SF3B1, AGXT, 2011 more genes
    nsv2778584copy number variation1nstd37humanLikely pathogenic GRCh37 (hg19) chr11: 64,501,919-67,129,258 , GRCh38 (hg38) chr11: 64,734,447-67,361,787 , NCBI36 (hg18) chr11: 64,258,495-66,885,834 ARL2, BBS1, 159 more genes
    nsv2776363copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr2: 12,771-242,783,384 , GRCh38 (hg38) chr2: 12,771-241,841,232 , NCBI36 (hg18) chr2: 2,771-242,432,057 SF3B1, LOC112268419, 3855 more genes
    nsv2773620copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr2: 194,581,315-201,752,422 , GRCh38 (hg38) chr2: 193,716,591-200,887,699 , NCBI36 (hg18) chr2: 194,289,560-201,460,667 SF3B1, HSPE1, 91 more genes
    nsv2772356copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr2: 50,739,936-242,751,149 , GRCh37 (hg19) chr2: 50,886,432-243,102,476 , GRCh38 (hg38) chr2: 50,659,294-242,157,305 SF3B1, AAMP, 3095 more genes
    nsv2771794copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr2: 169,829,974-215,521,436 , GRCh38 (hg38) chr2: 168,973,464-214,656,712 , NCBI36 (hg18) chr2: 169,538,220-215,229,681 SF3B1, CHRNA1, 659 more genes
    nsv2770864copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chr2: 130,861,065-242,751,149 , GRCh37 (hg19) chr2: 131,144,595-243,102,476 , GRCh38 (hg38) chr2: 130,387,022-242,157,305 SF3B1, ACVR2A, 1698 more genes
    nsv2770252copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr11: 230,616-134,938,470 , GRCh38 (hg38) chr11: 230,616-135,068,576 , NCBI36 (hg18) chr11: 220,616-134,443,680 LOC105369335, MIR5691, 2904 more genes
    nsv2057296short tandem repeat1nstd128human GRCh37 (hg19) chr2: 198,293,045-198,293,070 , GRCh38 (hg38) chr2: 197,428,321-197,428,346 SF3B1
    nsv2057295short tandem repeat1nstd128human GRCh37 (hg19) chr2: 198,290,194-198,290,228 , GRCh38 (hg38) chr2: 197,425,470-197,425,504 SF3B1
    nsv2057294short tandem repeat1nstd128human GRCh37 (hg19) chr2: 198,289,880-198,289,902 , GRCh38 (hg38) chr2: 197,425,156-197,425,178 SF3B1
    nsv2057293short tandem repeat4nstd128human GRCh37 (hg19) chr2: 198,289,218-198,289,234 , GRCh38 (hg38) chr2: 197,424,494-197,424,510 SF3B1
    nsv2057292short tandem repeat2nstd128human GRCh37 (hg19) chr2: 198,287,316-198,287,331 , GRCh38 (hg38) chr2: 197,422,592-197,422,607 SF3B1
    nsv2057291short tandem repeat4nstd128human GRCh37 (hg19) chr2: 198,280,858-198,280,870 , GRCh38 (hg38) chr2: 197,416,134-197,416,146 SF3B1
    nsv2057290short tandem repeat2nstd128human GRCh37 (hg19) chr2: 198,274,125-198,274,136 , GRCh38 (hg38) chr2: 197,409,401-197,409,412 SF3B1
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