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Items: 1 to 20 of 123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv5839616copy number variation1nstd209human GRCh38 chr4: 48,481,362-48,483,953 , GRCh37.p13 chr4: 48,483,379-48,485,970 SLC10A4
    nsv5084968mobile element insertion1nstd203human GRCh38 chr4: 48,481,402-48,481,413 , GRCh37.p13 chr4: 48,483,419-48,483,430 SLC10A4
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4791614copy number variation1nstd200human GRCh37 chr4: 43,358,175-53,119,711 , GRCh38.p12 chr4: 43,356,158-52,253,545 , LOC107986277, 78 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4684161copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-49,620,898 , GRCh38.p12 chr4: 49,556-49,618,881 TLR10, WDR1, 669 more genes
    nsv4680751copy number variation1nstd189human GRCh37.p13 chr4: 48,107,459-49,309,854 , GRCh38.p12 chr4: 48,105,442-49,307,837 TEC, TXK, 19 more genes
    nsv4588825copy number variation1nstd183human GRCh37 chr4: 48,408,821-48,674,943 , GRCh38.p12 chr4: 48,406,804-48,672,926 SLAIN2, SLC10A4, 4 more genes
    nsv4588703copy number variation1nstd183human GRCh37 chr4: 48,482,588-48,583,965 , GRCh38.p12 chr4: 48,480,571-48,581,948 SLC10A4, ZAR1, 2 more genes
    nsv4521145copy number variation1nstd166human GRCh37.p13 chr4: 47,873,999-48,666,000 , GRCh38.p12 chr4: 47,871,982-48,663,983 NFXL1, ZAR1, 13 more genes
    nsv4108089copy number variation1nstd166human GRCh37.p13 chr4: 48,485,319-48,486,019 , GRCh38.p12 chr4: 48,483,302-48,484,002 SLC10A4
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