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Items: 1 to 20 of 33

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3906260copy number variation1nstd102humanBenign GRCh37 chr7: 38,626,205-38,634,185 , GRCh38.p12 chr7: 38,586,605-38,594,585 AMPH
    nsv3909643copy number variation1nstd102humanBenign GRCh37 chr7: 38,626,205-38,630,433 , GRCh38.p12 chr7: 38,586,605-38,590,833 AMPH
    nsv3897629copy number variation1nstd102humanBenign GRCh37 chr7: 38,626,035-38,626,399 , GRCh38.p12 chr7: 38,586,435-38,586,799 AMPH
    nsv3906479copy number variation1nstd102humanBenign GRCh37 chr7: 38,626,087-38,626,399 , GRCh38.p12 chr7: 38,586,487-38,586,799 AMPH
    nsv3897447copy number variation1nstd102humanBenign GRCh37 chr7: 38,626,147-38,626,399 , GRCh38.p12 chr7: 38,586,547-38,586,799 AMPH
    nsv3899784copy number variation1nstd102humanBenign GRCh37 chr7: 38,626,147-38,626,347 , GRCh38.p12 chr7: 38,586,547-38,586,747 AMPH
    nsv3902186copy number variation1nstd102humanBenign GRCh37 chr7: 38,626,147-38,626,295 , GRCh38.p12 chr7: 38,586,547-38,586,695 AMPH
    nsv4675748copy number variation1nstd102humanUncertain significance GRCh37 chr7: 38,559,831-38,733,061 , GRCh38.p12 chr7: 38,520,231-38,693,461 AMPH, KRT8P20, 2 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 AMPH, RNU6-438P, 2682 more genes
    nsv3888815copy number variation1nstd102humanPathogenic GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467 AMPH, LOC107986817, 2014 more genes
    nsv3897424copy number variation1nstd102humanPathogenic GRCh37 chr7: 32,911,003-44,576,005 , GRCh38.p12 chr7: 32,871,391-44,536,406 AMPH, LOC107986734, 192 more genes
    nsv3916442copy number variation1nstd102humanPathogenic NCBI36 chr7: 37,309,607-48,670,880 , GRCh37 chr7: 37,343,082-48,700,334 , GRCh38 chr7: 37,303,478-48,660,738 AMPH, LOC102724903, 204 more genes
    nsv3912277copy number variation1nstd102humanPathogenic NCBI36 chr7: 32,684,528-41,051,106 , GRCh37 chr7: 32,718,003-41,084,581 , GRCh38 chr7: 32,678,391-41,044,983 AMPH, MATCAP2, 134 more genes
    nsv3924742copy number variation1nstd102humanPathogenic GRCh37 chr7: 38,217,601-45,343,699 , GRCh38 chr7: 38,177,999-45,304,100 , NCBI36 chr7: 38,184,126-45,310,224 AMPH, NUDCD3, 152 more genes
    nsv3912038copy number variation1nstd102humanPathogenic GRCh38 chr7: 35,460,776-42,013,800 , NCBI36 chr7: 35,466,911-42,019,924 , GRCh37 chr7: 35,500,386-42,053,399 AMPH, INHBA-AS1, 110 more genes
    nsv3894780copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842 AMPH, RNU6-565P, 2684 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 AMPH, RPL23AP51, 2684 more genes
    nsv3909087copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620 AMPH, MNX1-AS2, 2682 more genes
    nsv3908592copy number variation2nstd102humanPathogenic GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017 AMPH, TRGV3, 2682 more genes
    nsv3915802copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-41,915,483 , GRCh38 chr7: 54,185-41,875,885 , NCBI36 chr7: 149,268-41,882,008 AMPH, RPL23AP52, 638 more genes
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