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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4359167copy number variation1nstd102humanUncertain significance NCBI36 (hg18) chr3: 12,504,064-13,013,825 , GRCh37.p13 chr3: 12,529,064-13,038,825 , GRCh38.p12 chr3: 12,487,565-12,997,325 IQSEC1, MKRN2OS, 16 more genes
    nsv4358751copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr3: 48,914-20,350,883 , GRCh37.p13 chr3: 73,914-20,375,879 , GRCh38.p12 chr3: 32,241-20,334,387 IQSEC1, ATP2B2, 289 more genes
    nsv4356308copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr3: 48,914-30,080,703 , GRCh37.p13 chr3: 73,914-30,105,699 , GRCh38.p12 chr3: 32,241-30,064,208 IQSEC1, ITPR1, 382 more genes
    nsv4355924copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr3: 11,479,802-38,936,038 , GRCh37.p13 chr3: 11,504,802-38,961,034 , GRCh38.p12 chr3: 11,463,328-38,919,543 IQSEC1, ACVR2B, 365 more genes
    nsv4355587copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr3: 80,526-19,527,096 , GRCh37.p13 chr3: 105,526-19,552,092 , GRCh38.p12 chr3: 63,843-19,510,600 IQSEC1, DAZL, 274 more genes
    nsv4354479copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr3: 68,749-20,296,623 , GRCh37.p13 chr3: 93,749-20,321,619 , GRCh38.p12 chr3: 52,066-20,280,127 IQSEC1, GRM7, 289 more genes
    nsv4354160copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr3: 48,914-13,630,319 , GRCh37.p13 chr3: 73,914-13,655,318 , GRCh38.p12 chr3: 32,241-13,613,818 IQSEC1, ITPR1, 184 more genes
    nsv4354080copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr3: 68,949-37,164,571 , GRCh37.p13 chr3: 93,949-37,189,567 , GRCh38.p12 chr3: 52,266-37,148,076 IQSEC1, BTD, 470 more genes
    nsv4347648copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr3: 7,397,797-14,401,942 , GRCh38.p12 chr3: 7,356,110-14,360,442 , NCBI36 (hg18) chr3: 7,372,797-14,376,946 IQSEC1, OGG1, 135 more genes
    nsv4347609copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr3: 94,991-41,423,012 , GRCh38.p12 chr3: 53,308-41,381,521 , NCBI36 (hg18) chr3: 69,991-41,398,016 IQSEC1, BTD, 561 more genes
    nsv4338929mobile element insertion1nstd166human GRCh37.p13 chr3: 12,938,182-12,938,197 , GRCh38.p12 chr3: 12,896,683-12,896,698 IQSEC1, LOC105376956
    nsv4333104mobile element insertion1nstd166human GRCh37.p13 chr3: 4,693,154-48,251,928 , GRCh38.p12 chr3: 4,651,470-48,210,438 IQSEC1, CCR1, 690 more genes
    nsv4290814insertion1nstd166human GRCh37.p13 chr3: 11,700,123-76,122,427 , GRCh38.p12 chr3: 11,658,649-76,073,276 IQSEC1, ACVR2B, 1081 more genes
    nsv4288812insertion1nstd166human GRCh37.p13 chr3: 1,814,578-159,651,175 , GRCh38.p12 chr3: 1,772,894-159,933,387 IQSEC1, ACTG1P1, 2335 more genes
    nsv4285987insertion1nstd166human GRCh37.p13 chr3: 13,061,228-13,061,228 , GRCh38.p12 chr3: 13,019,728-13,019,728 IQSEC1
    nsv4282799insertion1nstd166human GRCh37.p13 chr3: 12,968,922-12,968,985 , GRCh38.p12 chr3: 12,927,422-12,927,485 IQSEC1, LOC105376956
    nsv4278620insertion1nstd166human GRCh37.p13 chr3: 12,968,861-12,968,883 , GRCh38.p12 chr3: 12,927,361-12,927,383 IQSEC1, LOC105376956
    nsv4275350insertion1nstd166human GRCh37.p13 chr3: 12,968,883-12,968,923 , GRCh38.p12 chr3: 12,927,383-12,927,423 IQSEC1, LOC105376956
    nsv4273162insertion1nstd166human GRCh37.p13 chr3: 12,968,844-12,968,928 , GRCh38.p12 chr3: 12,927,344-12,927,428 IQSEC1, LOC105376956
    nsv4089900copy number variation1nstd166human GRCh37.p13 chr3: 12,980,032-12,980,088 , GRCh38.p12 chr3: 12,938,532-12,938,588 IQSEC1, LOC105376956
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