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Items: 1 to 20 of 24

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    Number of Variants: 20

    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 STARD3NL, 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 STARD3NL, LOC107986817, 2014 more genes
    nsv3897424copy number variation1nstd102humanPathogenic GRCh37 chr7: 32,911,003-44,576,005 , GRCh38.p12 chr7: 32,871,391-44,536,406 STARD3NL, 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 STARD3NL, 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 STARD3NL, 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 STARD3NL, 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 STARD3NL, INHBA-AS1, 110 more genes
    nsv3894780copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842 STARD3NL, RNU6-565P, 2684 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 STARD3NL, RPL23AP51, 2684 more genes
    nsv3909087copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620 STARD3NL, MNX1-AS2, 2682 more genes
    nsv3908592copy number variation2nstd102humanPathogenic GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017 STARD3NL, 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 STARD3NL, RPL23AP52, 638 more genes
    nsv3899194copy number variation1nstd102humanPathogenic GRCh37 chr7: 11,048,840-52,863,626 , GRCh38.p12 chr7: 11,009,213-52,795,933 STARD3NL, BRWD1P3, 590 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 STARD3NL, MIR4649, 444 more genes
    nsv3898448copy number variation1nstd102humanPathogenic GRCh37 chr7: 30,463,886-43,470,805 , GRCh38.p12 chr7: 30,424,270-43,431,206 STARD3NL, INMT, 193 more genes
    nsv3895187copy number variation1nstd102humanPathogenic GRCh37 chr7: 37,213,108-40,255,122 , GRCh38.p12 chr7: 37,173,503-40,215,523 STARD3NL, LOC107986785, 66 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 STARD3NL, AOC1, 2682 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 STARD3NL, 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 STARD3NL, ADCYAP1R1, 175 more genes
    nsv3904856copy number variation1nstd102humanBenign GRCh37 chr7: 38,043,677-38,501,065 , GRCh38.p12 chr7: 38,004,075-38,461,465 STARD3NL, TRGV9, 26 more genes
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