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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3923126copy number variation1nstd102humanUncertain significance NCBI36 (hg18) chr16: 35,006,660-45,286,576 , GRCh37.p13 chr16: 35,149,159-46,729,075 , GRCh38.p12 chr16: 35,914,788-46,695,163 VPS35, LOC441768, 7 more genes
    nsv3921269copy number variation1nstd102humanPathogenic NCBI36 (hg18) chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 AGRP, GAS8-AS1, 1007 more genes
    nsv3920484copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr16: 46,466,829-51,673,196 , GRCh37.p13 chr16: 46,500,741-51,707,107 , NCBI36 (hg18) chr16: 45,058,242-50,264,608 CBLN1, N4BP1, 95 more genes
    nsv3917427copy number variation1nstd102humanBenign NCBI36 (hg18) chr16: 32,529,496-88,822,254 , GRCh37.p13 chr16: 32,621,995-90,294,753 , GRCh38.p12 chr16: 32,610,674-90,228,345 AFG3L1P, AGRP, 991 more genes
    nsv3916905copy number variation1nstd102humanBenign NCBI36 (hg18) chr16: 32,481,314-88,822,254 , GRCh37.p13 chr16: 32,573,813-90,294,753 , GRCh38.p12 chr16: 32,562,492-90,228,345 CBFA2T3, CDH16, 991 more genes
    nsv3916044copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr16: 46,466,829-52,355,793 , GRCh37.p13 chr16: 46,500,741-52,389,705 , NCBI36 (hg18) chr16: 45,058,242-50,947,206 ADAM3B, SIAH1, 105 more genes
    nsv3915496copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr16: 46,471,520-52,405,956 , GRCh37.p13 chr16: 46,505,432-52,439,868 , NCBI36 (hg18) chr16: 45,062,933-50,997,369 ADAM3B, SIAH1, 105 more genes
    nsv3915341copy number variation1nstd102humanBenign NCBI36 (hg18) chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 AARS, AP1G1, 1007 more genes
    nsv3915118copy number variation1nstd102humanBenign NCBI36 (hg18) chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 AGRP, BBS2, 1007 more genes
    nsv3914752copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr16: 46,466,829-51,939,304 , GRCh37.p13 chr16: 46,500,741-51,973,216 , NCBI36 (hg18) chr16: 45,058,242-50,530,717 ADCY7, CYLD, 97 more genes
    nsv3914703copy number variation1nstd102humanLikely benign GRCh38 (hg38) chr16: 46,471,685-46,767,956 , GRCh37.p13 chr16: 46,505,597-46,801,868 , NCBI36 (hg18) chr16: 45,063,098-45,359,369 ANKRD26P1, RAB43P1, 7 more genes
    nsv3912769copy number variation1nstd102humanBenign NCBI36 (hg18) chr16: 31,862,658-88,822,254 , GRCh37.p13 chr16: 31,955,157-90,294,753 , GRCh38.p12 chr16: 31,943,836-90,228,345 AARS, APRT, 1007 more genes
    nsv3912663copy number variation1nstd102humanBenign NCBI36 (hg18) chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 ADCY7, AGRP, 1007 more genes
    nsv3912156copy number variation1nstd102humanBenign NCBI36 (hg18) chr16: 31,902,168-88,822,254 , GRCh37.p13 chr16: 31,994,667-90,294,753 , GRCh38.p12 chr16: 31,983,346-90,228,345 AFG3L1P, CBFA2T3, 1007 more genes
    nsv3911727copy number variation1nstd102humanBenign NCBI36 (hg18) chr16: 31,902,168-88,822,254 , GRCh37.p13 chr16: 31,994,667-90,294,753 , GRCh38.p12 chr16: 31,983,346-90,228,345 ADCY7, AGRP, 1007 more genes
    nsv3911127copy number variation1nstd102humanBenign NCBI36 (hg18) chr16: 32,348,376-88,822,254 , GRCh37.p13 chr16: 32,440,875-90,294,753 , GRCh38.p12 chr16: 32,429,554-90,228,345 ADCY7, AP1G1, 994 more genes
    nsv3910120copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr16: 46,466,829-52,422,170 , GRCh37.p13 chr16: 46,500,741-52,456,082 , NCBI36 (hg18) chr16: 45,058,242-51,013,583 ADAM3B, SIAH1, 106 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 , NCBI36 (hg18) chr16: 28,165-88,690,776 ADCY7, AGRP, 1925 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 , NCBI36 (hg18) chr16: 1,451-88,822,133 ADCY9, AQP8, 1939 more genes
    nsv3906104copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr16: 46,464,488-90,155,062 , GRCh38.p12 chr16: 46,430,576-90,088,654 , NCBI36 (hg18) chr16: 45,021,989-88,682,563 AARS, AP1G1, 848 more genes
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