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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4359418copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr7: 149,268-158,767,840 , GRCh37.p13 chr7: 54,185-159,075,079 , GRCh38.p12 chr7: 54,185-159,282,390 AHR, AKR1B1, 2764 more genes
    nsv4358252copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr7: 1,704,286-27,213,439 , GRCh37.p13 chr7: 1,737,760-27,246,914 , GRCh38.p12 chr7: 1,698,124-27,207,295 ACTB, HOXA2, 380 more genes
    nsv4357703copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr7: 149,268-26,833,778 , GRCh37.p13 chr7: 54,185-26,867,253 , GRCh38.p12 chr7: 54,185-26,827,634 CLK2P1, GNA12, 405 more genes
    nsv4357616copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr7: 140,213-25,227,309 , GRCh37.p13 chr7: 45,130-25,260,784 , GRCh38.p12 chr7: 45,130-25,221,165 ACTB, IL6, 379 more genes
    nsv4356359copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr7: 9,981,805-19,363,026 , GRCh37.p13 chr7: 10,015,280-19,396,501 , GRCh38.p12 chr7: 9,975,653-19,356,878 AHR, PHF14, 90 more genes
    nsv4355598copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr7: 11,128,644-16,485,453 , GRCh37.p13 chr7: 11,162,119-16,518,928 , GRCh38.p12 chr7: 11,122,492-16,479,303 PHF14, THSD7A, 46 more genes
    nsv4355422copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr7: 10,616,221-25,766,705 , GRCh37.p13 chr7: 10,649,696-25,800,180 , GRCh38.p12 chr7: 10,610,069-25,760,560 CLK2P1, UBA52P1, 184 more genes
    nsv4354832copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr7: 149,068-158,767,981 , GRCh37.p13 chr7: 53,985-159,075,220 , GRCh38.p12 chr7: 53,985-159,282,531 AKR1B1, ASNS, 2764 more genes
    nsv4354708copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr7: 5,688,366-27,236,455 , GRCh37.p13 chr7: 5,721,840-27,269,930 , GRCh38.p12 chr7: 5,682,209-27,230,311 DGKB, ETV1, 306 more genes
    nsv4354384copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr7: 149,268-41,882,008 , GRCh37.p13 chr7: 54,185-41,915,483 , GRCh38.p12 chr7: 54,185-41,875,885 ACTB, CLK2P1, 662 more genes
    nsv4352789copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr7: 149,068-24,367,675 , GRCh37.p13 chr7: 53,985-24,401,150 , GRCh38.p12 chr7: 53,985-24,361,531 AHR, DGKB, 367 more genes
    nsv4352145copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr7: 149,268-37,095,842 , GRCh37.p13 chr7: 54,185-37,129,317 , GRCh38.p12 chr7: 54,185-37,089,712 SEPTIN7, CHN2, 575 more genes
    nsv4350906copy number variation1nstd102humanBenign NCBI36 (hg18) chr7: 12,115,485-12,659,557 , GRCh37.p13 chr7: 12,148,960-12,693,032 , GRCh38.p12 chr7: 12,109,334-12,653,407 SCIN, VWDE, 10 more genes
    nsv4350019copy number variation1nstd102humanUncertain significance GRCh37 (hg19) chr7: 11,221,210-12,462,629 , GRCh38.p12 chr7: 11,181,583-12,423,003 , NCBI36 (hg18) chr7: 11,187,735-12,429,154 NPM1P11, LOC100421595, 8 more genes
    nsv4349849copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr7: 43,360-27,236,023 , GRCh38.p12 chr7: 43,360-27,196,404 , NCBI36 (hg18) chr7: 138,443-27,202,548 CLK2P1, GNA12, 427 more genes
    nsv4310756insertion1nstd166human GRCh37.p13 chr7: 9,566,588-26,453,916 , GRCh38.p12 chr7: 9,526,958-26,414,296 DGKB, GSDME, 207 more genes
    nsv4306877insertion1nstd166human GRCh37.p13 chr7: 9,183,580-73,629,127 , GRCh38.p12 chr7: 9,143,950-74,214,797 SEPTIN7, CHN2, 1055 more genes
    nsv4306769insertion1nstd166human GRCh37.p13 chr7: 10,215,343-83,064,333 , GRCh38.p12 chr7: 10,175,716-83,435,017 CCT6A, SEPTIN7, 1186 more genes
    nsv4302132insertion1nstd166human GRCh37.p13 chr7: 3,200,189-35,671,361 , GRCh38.p12 chr7: 3,160,556-35,631,751 AHR, CHN2, 465 more genes
    nsv4301318insertion1nstd166human GRCh37.p13 chr7: 9,079,697-21,449,225 , GRCh38.p12 chr7: 9,040,067-21,409,607 AGR2, NPM1P13, 122 more genes
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