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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3169873copy number variation1nstd156human NCBI36 (hg18) chr11: 21,149,404-21,167,220 , GRCh38.p2 chr11: 21,171,282-21,189,098 , GRCh37.p13 chr11: 21,192,828-21,210,644 NELL1
    nsv3151934copy number variation1nstd151human GRCh37 (hg19) chr11: 18,050,709-22,777,504 , GRCh38 (hg38) chr11: 18,029,162-22,755,958 NELL1, FANCF, 84 more genes
    nsv3150963copy number variation1nstd151human GRCh37 (hg19) chr11: 21,581,732-21,596,573 , GRCh38 (hg38) chr11: 21,560,186-21,575,027 NELL1
    nsv3146374copy number variation1nstd151human GRCh37 (hg19) chr11: 20,981,975-21,135,265 , GRCh38 (hg38) chr11: 20,960,429-21,113,719 NELL1, RNA5SP336
    nsv3141407copy number variation1nstd151human GRCh37 (hg19) chr11: 20,621,216-21,135,265 , GRCh38 (hg38) chr11: 20,599,670-21,113,719 NELL1, RNA5SP336, 3 more genes
    nsv3141390copy number variation2nstd151human GRCh37 (hg19) chr11: 21,555,917-21,596,573 , GRCh38 (hg38) chr11: 21,534,371-21,575,027 NELL1
    nsv3139646copy number variation1nstd151human GRCh37 (hg19) chr11: 21,592,307-21,596,573 , GRCh38 (hg38) chr11: 21,570,761-21,575,027 NELL1
    nsv3113481copy number variation1nstd145human GRCh37 (hg19) chr11: 20,749,629-20,756,566 , GRCh38 (hg38) chr11: 20,728,083-20,735,020 NELL1
    nsv3111987copy number variation1nstd145human GRCh37 (hg19) chr11: 20,847,788-20,849,038 , GRCh38 (hg38) chr11: 20,826,242-20,827,492 NELL1
    nsv3073614mobile element insertion1nstd144human GRCh37 (hg19) chr11: 20,926,531-20,926,531 , GRCh38 (hg38) chr11: 20,904,985-20,904,985 NELL1, LOC105376585
    nsv3073495mobile element insertion1nstd144human GRCh37 (hg19) chr11: 21,267,064-21,267,064 , GRCh38 (hg38) chr11: 21,245,518-21,245,518 NELL1
    nsv3073494mobile element insertion1nstd144human GRCh37 (hg19) chr11: 20,703,894-20,703,894 , GRCh38 (hg38) chr11: 20,682,348-20,682,348 NELL1
    nsv3073472mobile element insertion1nstd144human GRCh37 (hg19) chr11: 21,582,229-21,582,229 , GRCh38 (hg38) chr11: 21,560,683-21,560,683 NELL1
    nsv3073470copy number variation1nstd144human GRCh37 (hg19) chr11: 20,916,539-20,916,861 , GRCh38 (hg38) chr11: 20,894,993-20,895,315 NELL1, LOC105376585
    nsv3073381mobile element insertion1nstd144human GRCh37 (hg19) chr11: 20,730,250-20,730,250 , GRCh38 (hg38) chr11: 20,708,704-20,708,704 NELL1
    nsv3071186insertion1nstd90human GRCh37 (hg19) chr11: 20,795,541-20,795,541 , GRCh38 (hg38) chr11: 20,773,995-20,773,995 NELL1
    esv4010042copy number variation1estd232humanPathogenic GRCh37 (hg19) chr11: 21,586,131-33,168,232 , GRCh38 (hg38) chr11: 21,564,585-33,146,686 NELL1, BDNF, 119 more genes
    esv4010040copy number variation1estd232humanPathogenic GRCh37 (hg19) chr11: 18,536,224-31,923,308 , GRCh38 (hg38) chr11: 18,514,677-31,901,762 NELL1, BDNF, 142 more genes
    nsv3065846insertion1nstd140human GRCh37 (hg19) chr11: 21,338,971-21,338,972 , GRCh38 (hg38) chr11: 21,317,425-21,317,426 NELL1
    nsv3052401insertion1nstd140human GRCh38 (hg38) chr11: 21,317,433-21,317,434 , GRCh37 (hg19) chr11: 21,338,979-21,338,980 NELL1
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