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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3924159copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr7: 53,985-159,282,531 , GRCh37.p13 chr7: 53,985-159,075,220 , NCBI36 (hg18) chr7: 149,068-158,767,981 AHR, AKR1B1, 2765 more genes
    nsv3922815copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr7: 97,419,852-158,923,762 , GRCh37.p13 chr7: 97,049,164-158,716,453 , NCBI36 (hg18) chr7: 96,887,100-158,409,214 ACHE, AZGP1, 1207 more genes
    nsv3922535copy number variation1nstd102humanLikely benign GRCh38 (hg38) chr7: 99,195,836-100,348,063 , GRCh37.p13 chr7: 98,793,459-99,945,686 , NCBI36 (hg18) chr7: 98,631,395-99,783,622 CYP3A51P, PMS2P1, 67 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr7: 54,185-159,282,390 , GRCh37.p13 chr7: 54,185-159,075,079 , NCBI36 (hg18) chr7: 149,268-158,767,840 AHR, AKR1B1, 2765 more genes
    nsv3916333copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr7: 98,288,474-101,259,804 , GRCh37.p13 chr7: 97,917,786-100,903,085 , NCBI36 (hg18) chr7: 97,755,722-100,689,805 CYP3A7, MCM7, 144 more genes
    nsv3915692copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr7: 99,195,836-102,258,175 , GRCh37.p13 chr7: 98,793,459-101,718,950 , NCBI36 (hg18) chr7: 98,631,395-101,688,175 CYP3A4, LRCH4, 139 more genes
    nsv3915383copy number variation1nstd102humanPathogenic GRCh38 (hg38) chr7: 99,219,420-100,902,269 , GRCh37.p13 chr7: 98,817,043-100,499,889 , NCBI36 (hg18) chr7: 98,654,979-100,337,825 CYP3A51P, EPHB4, 107 more genes
    nsv3909087copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620 , NCBI36 (hg18) chr7: 140,018-158,819,071 ADCY1, AEBP1, 2765 more genes
    nsv3908872copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 , NCBI36 (hg18) chr7: 138,443-158,812,468 AOC1, AHR, 2765 more genes
    nsv3908592copy number variation2nstd102humanPathogenic GRCh37 (hg19) chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017 , NCBI36 (hg18) chr7: 138,444-158,812,468 AKR1B1, AMPH, 2765 more genes
    nsv3903311copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr7: 98,847,725-102,472,176 , GRCh38.p12 chr7: 99,250,102-102,831,729 , NCBI36 (hg18) chr7: 98,685,661-102,259,412 ACHE, AZGP1, 167 more genes
    nsv3896396copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr7: 98,969,247-159,119,707 , GRCh38.p12 chr7: 99,371,624-159,327,017 , NCBI36 (hg18) chr7: 98,807,183-158,812,468 AKR1B1, CALD1, 1171 more genes
    nsv3894780copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842 , NCBI36 (hg18) chr7: 103,461-158,815,293 ARF5, BLVRA, 2768 more genes
    nsv3894097copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr7: 98,693,388-159,119,707 , GRCh38.p12 chr7: 99,095,765-159,327,017 , NCBI36 (hg18) chr7: 98,531,324-158,812,468 AKR1B1, ALDH7A1P3, 1176 more genes
    nsv3892887copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr7: 92,445,452-99,686,985 , GRCh38.p12 chr7: 92,816,138-100,089,362 , NCBI36 (hg18) chr7: 92,283,388-99,524,921 AZGP1, DLX5, 154 more genes
    nsv3891081copy number variation1nstd102humanUncertain significance GRCh37 (hg19) chr7: 98,985,840-99,171,421 , GRCh38.p12 chr7: 99,388,217-99,573,798 , NCBI36 (hg18) chr7: 98,823,776-99,009,357 BUD31, ARPC1B, 15 more genes
    nsv3888815copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467 , NCBI36 (hg18) chr7: 12,224,672-140,140,736 AHR, AKR1B1, 2074 more genes
    nsv3135126copy number variation1nstd151human GRCh37 (hg19) chr7: 98,941,913-99,751,355 , GRCh38.p12 chr7: 99,344,290-100,153,732 CYP3A51P, ZNF3, 50 more genes
    nsv3124926copy number variation1nstd151human GRCh37 (hg19) chr7: 98,930,974-99,381,709 , GRCh38.p12 chr7: 99,333,351-99,784,086 CYP3A7, BUD31, 24 more genes
    nsv3119605copy number variation1nstd151human GRCh37 (hg19) chr7: 86,394,459-108,524,594 , GRCh38.p12 chr7: 86,765,143-108,884,537 AZGP1, AP1S1, 450 more genes
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