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Items: 1 to 20 of 26

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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 TRAPPC14, 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 TRAPPC14, LOC107986817, 2014 more genes
    nsv6313503copy number variation1nstd102humanPathogenic GRCh37 chr7: 99,417,471-111,586,308 , GRCh38.p12 chr7: 99,819,848-111,946,253 TRAPPC14, GJC3, 237 more genes
    nsv3903311copy number variation1nstd102humanPathogenic GRCh37 chr7: 98,847,725-102,472,176 , GRCh38.p12 chr7: 99,250,102-102,831,729 TRAPPC14, PLOD3, 163 more genes
    nsv3915692copy number variation1nstd102humanPathogenic GRCh38 chr7: 99,195,836-102,258,175 , NCBI36 chr7: 98,631,395-101,688,175 , GRCh37 chr7: 98,793,459-101,718,950 TRAPPC14, MUC17, 135 more genes
    nsv7148181copy number variation1nstd102humanPathogenic GRCh38 chr7: 98,454,022-100,723,798 , GRCh37.p13 chr7: 98,083,334-100,321,421 TRAPPC14, LAMTOR4, 107 more genes
    nsv6312372copy number variation1nstd102humanPathogenic GRCh37 chr7: 98,983,338-100,860,555 , GRCh38.p12 chr7: 99,385,715-101,217,274 TRAPPC14, AZGP1P1, 119 more genes
    nsv3915383copy number variation1nstd102humanPathogenic NCBI36 chr7: 98,654,979-100,337,825 , GRCh38 chr7: 99,219,420-100,902,269 , GRCh37 chr7: 98,817,043-100,499,889 TRAPPC14, GNB2, 104 more genes
    nsv3894780copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842 TRAPPC14, RNU6-565P, 2684 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 TRAPPC14, RPL23AP51, 2684 more genes
    nsv3909087copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620 TRAPPC14, MNX1-AS2, 2682 more genes
    nsv3908592copy number variation2nstd102humanPathogenic GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017 TRAPPC14, TRGV3, 2682 more genes
    nsv3922815copy number variation1nstd102humanPathogenic NCBI36 chr7: 96,887,100-158,409,214 , GRCh38 chr7: 97,419,852-158,923,762 , GRCh37 chr7: 97,049,164-158,716,453 TRAPPC14, SEPTIN7P6, 1175 more genes
    nsv3894097copy number variation1nstd102humanPathogenic GRCh37 chr7: 98,693,388-159,119,707 , GRCh38.p12 chr7: 99,095,765-159,327,017 TRAPPC14, CYP3A5, 1144 more genes
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 TRAPPC14, ARPC1A, 265 more genes
    nsv3916333copy number variation1nstd102humanPathogenic GRCh37 chr7: 97,917,786-100,903,085 , GRCh38 chr7: 98,288,474-101,259,804 , NCBI36 chr7: 97,755,722-100,689,805 TRAPPC14, ZCWPW1, 141 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 TRAPPC14, AOC1, 2682 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 TRAPPC14, ACHE, 1532 more genes
    nsv4684274copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 99,593,346-102,470,275 , GRCh38.p12 chr7: 99,995,723-102,829,828 TRAPPC14, ACHE, 124 more genes
    nsv3922535copy number variation1nstd102humanLikely benign NCBI36 chr7: 98,631,395-99,783,622 , GRCh37 chr7: 98,793,459-99,945,686 , GRCh38 chr7: 99,195,836-100,348,063 TRAPPC14, LAMTOR4, 66 more genes
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