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Items: 1 to 20 of 452

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093619copy number variation1nstd228human GRCh37 chr4: 171,508,974-190,957,473 , GRCh38.p12 chr4: 170,587,823-190,036,318 AGA, SLC25A4, 240 more genes
    nsv7041729inversion1nstd229human GRCh38 chr4: 188,997,516-189,799,870 , GRCh37.p13 chr4: 189,918,670-190,721,024 LOC105377615, LOC105377612, 8 more genes
    nsv7041283inversion1nstd229human GRCh38 chr4: 189,258,161-189,709,818 , GRCh37.p13 chr4: 190,179,315-190,630,972 HSP90AA4P, LOC105377615, 4 more genes
    nsv7038647inversion1nstd229human GRCh38 chr4: 188,362,708-189,560,580 , GRCh37.p13 chr4: 189,283,862-190,481,734 LOC101930028, LOC105377611, 13 more genes
    nsv6775659copy number variation1nstd229human GRCh38 chr4: 189,472,026-189,476,775 , GRCh37.p13 chr4: 190,393,180-190,397,929 HSP90AA4P
    nsv6774285copy number variation1nstd229human GRCh38 chr4: 189,084,401-189,474,800 , GRCh37.p13 chr4: 190,005,555-190,395,954 LOC105377613, HSP90AA4P, 2 more genes
    nsv6772677copy number variation1nstd229human GRCh38 chr4: 189,470,601-189,476,800 , GRCh37.p13 chr4: 190,391,755-190,397,954 HSP90AA4P
    nsv6772481copy number variation1nstd229human GRCh38 chr4: 189,161,433-189,830,798 , GRCh37.p13 chr4: 190,082,587-190,751,953 LOC105377614, LINC01262, 6 more genes
    nsv6768072copy number variation1nstd229human GRCh38 chr4: 189,133,055-189,757,355 , GRCh37.p13 chr4: 190,054,209-190,678,509 LINC01262, LOC105377616, 4 more genes
    nsv6763289copy number variation1nstd229human GRCh38 chr4: 189,472,401-189,476,800 , GRCh37.p13 chr4: 190,393,555-190,397,954 HSP90AA4P
    nsv6763252copy number variation1nstd229human GRCh38 chr4: 189,171,161-189,606,993 , GRCh37.p13 chr4: 190,092,315-190,528,147 LOC105377614, HSP90AA4P, 1 more genes
    nsv6762345copy number variation1nstd229human GRCh38 chr4: 189,377,722-189,621,455 , GRCh37.p13 chr4: 190,298,876-190,542,609 HSP90AA4P, LOC105377614, 1 more genes
    nsv6758741copy number variation1nstd229human GRCh38 chr4: 189,475,969-189,488,009 , GRCh37.p13 chr4: 190,397,123-190,409,163 HSP90AA4P
    nsv6636995copy number variation1nstd102humanUncertain significance GRCh37 chr4: 187,853,428-190,957,473 , GRCh38.p12 chr4: 186,932,274-190,036,318 LINC02515, LINC02514, 49 more genes
    nsv6636301copy number variation1nstd102humanPathogenic GRCh37 chr4: 183,694,501-190,957,473 , GRCh38.p12 chr4: 182,773,348-190,036,318 LOC105377588, ENPP6, 139 more genes
    nsv6634364copy number variation1nstd102humanPathogenic GRCh37 chr4: 167,779,888-190,957,473 , GRCh38.p12 chr4: 166,858,737-190,036,318 LOC101928551, LOC107986330, 279 more genes
    nsv6634351copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318 COPS3P1, LOC339975, 363 more genes
    nsv6634350copy number variation1nstd102humanPathogenic GRCh37 chr4: 185,211,271-190,957,473 , GRCh38.p12 chr4: 184,290,118-190,036,318 LINC02374, SLED1, 102 more genes
    nsv6629661copy number variation2nstd224human GRCh37 chr4: 190,278,973-190,469,858 , GRCh38.p12 chr4: 189,357,819-189,548,704 , GRCh38.p12 chr4|NT_187679.1: 1-186,926 LOC105377614, HSP90AA4P
    nsv6629659copy number variation1nstd224human GRCh37 chr4: 189,959,922-190,477,265 , GRCh38.p12 chr4: 189,038,768-189,556,111 HSP90AA4P, LOC105377611, 4 more genes
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