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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7098818copy number variation1nstd102humanPathogenic GRCh38 chr4: 11,399,082-38,137,335 , GRCh37.p13 chr4: 11,400,706-38,138,956 LOC105374542, PPARGC1A, 232 more genes
    nsv7049186inversion1nstd229human GRCh38 chr4: 38,135,041-40,245,309 , GRCh37.p13 chr4: 38,136,662-40,246,929 SMIM14, RNU6-887P, 42 more genes
    nsv7042342inversion1nstd229human GRCh38 chr4: 38,068,537-38,070,528 , GRCh37.p13 chr4: 38,070,158-38,072,149 TBC1D1
    nsv6735855copy number variation1nstd229human GRCh38 chr4: 37,893,756-37,917,056 , GRCh37.p13 chr4: 37,895,377-37,918,677 TBC1D1
    nsv6734483copy number variation1nstd229human GRCh38 chr4: 38,118,485-38,141,310 , GRCh37.p13 chr4: 38,120,106-38,142,931 TBC1D1
    nsv6734438copy number variation1nstd229human GRCh38 chr4: 38,017,451-38,044,265 , GRCh37.p13 chr4: 38,019,072-38,045,886 TBC1D1
    nsv6734406copy number variation1nstd229human GRCh38 chr4: 38,135,001-38,474,700 , GRCh37.p13 chr4: 38,136,622-38,476,321 LOC105374409, TBC1D1, 3 more genes
    nsv6732700copy number variation1nstd229human GRCh38 chr4: 37,943,104-37,979,324 , GRCh37.p13 chr4: 37,944,725-37,980,945 PTTG2, TBC1D1
    nsv6732632copy number variation1nstd229human GRCh38 chr4: 37,899,142-37,899,627 , GRCh37.p13 chr4: 37,900,763-37,901,248 TBC1D1
    nsv6731885copy number variation1nstd229human GRCh38 chr4: 38,085,404-38,085,499 , GRCh37.p13 chr4: 38,087,025-38,087,120 TBC1D1
    nsv6730316copy number variation1nstd229human GRCh38 chr4: 38,138,003-38,139,058 , GRCh37.p13 chr4: 38,139,624-38,140,679 TBC1D1
    nsv6728083copy number variation1nstd229human GRCh38 chr4: 38,083,701-38,088,000 , GRCh37.p13 chr4: 38,085,322-38,089,621 TBC1D1
    nsv6728066copy number variation1nstd229human GRCh38 chr4: 38,095,151-38,095,523 , GRCh37.p13 chr4: 38,096,772-38,097,144 TBC1D1
    nsv6727581copy number variation1nstd229human GRCh38 chr4: 28,550,139-38,411,880 , GRCh37.p13 chr4: 28,551,761-38,413,501 LINC02497, MESTP3, 66 more genes
    nsv6726404copy number variation1nstd229human GRCh38 chr4: 37,991,536-38,012,340 , GRCh37.p13 chr4: 37,993,157-38,013,961 TBC1D1, PSME2P4, 1 more genes
    nsv6725894copy number variation1nstd229human GRCh38 chr4: 37,882,705-37,948,392 , GRCh37.p13 chr4: 37,884,326-37,950,013 TBC1D1
    nsv6724290copy number variation1nstd229human GRCh38 chr4: 38,129,767-38,130,151 , GRCh37.p13 chr4: 38,131,388-38,131,772 TBC1D1
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