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Items: 19

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    Number of Variants: 19

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 HERPUD2, 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 HERPUD2, LOC107986817, 2014 more genes
    nsv3897424copy number variation1nstd102humanPathogenic GRCh37 chr7: 32,911,003-44,576,005 , GRCh38.p12 chr7: 32,871,391-44,536,406 HERPUD2, LOC107986734, 192 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 HERPUD2, MATCAP2, 134 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 HERPUD2, INHBA-AS1, 110 more genes
    nsv3894780copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842 HERPUD2, RNU6-565P, 2684 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 HERPUD2, RPL23AP51, 2684 more genes
    nsv3909087copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620 HERPUD2, MNX1-AS2, 2682 more genes
    nsv3908592copy number variation2nstd102humanPathogenic GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017 HERPUD2, 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 HERPUD2, RPL23AP52, 638 more genes
    nsv3899194copy number variation1nstd102humanPathogenic GRCh37 chr7: 11,048,840-52,863,626 , GRCh38.p12 chr7: 11,009,213-52,795,933 HERPUD2, BRWD1P3, 590 more genes
    nsv3918785copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-37,129,317 , NCBI36 chr7: 149,268-37,095,842 , GRCh38 chr7: 54,185-37,089,712 HERPUD2, MMD2, 554 more genes
    nsv3917263copy number variation1nstd102humanPathogenic GRCh38 chr7: 33,328,312-62,377,476 , GRCh37 chr7: 33,367,924-61,831,899 , NCBI36 chr7: 33,334,449-61,469,334 HERPUD2, MIR4649, 444 more genes
    nsv3895449copy number variation1nstd102humanPathogenic GRCh37 chr7: 11,562,624-36,395,416 , GRCh38.p12 chr7: 11,522,997-36,355,807 HERPUD2, HOXA7, 343 more genes
    nsv3898448copy number variation1nstd102humanPathogenic GRCh37 chr7: 30,463,886-43,470,805 , GRCh38.p12 chr7: 30,424,270-43,431,206 HERPUD2, INMT, 193 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 HERPUD2, AOC1, 2682 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 HERPUD2, ACHE, 1532 more genes
    nsv6313670copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 27,507,832-39,072,473 , GRCh38.p12 chr7: 27,468,213-39,032,873 HERPUD2, ADCYAP1R1, 175 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 HERPUD2, RRBP1P1, 2680 more genes
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