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Items: 1 to 20 of 264

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140200copy number variation1nstd232human GRCh37.p13 chr5: 149,463,927-149,464,029 , GRCh38.p12 chr5: 150,084,364-150,084,466 CSF1R
    nsv7097513copy number variation1nstd102humanUncertain significance GRCh37 chr5: 147,774,340-149,681,936 , GRCh38.p12 chr5: 148,394,777-150,302,373 CSNK1A1, SLC26A2, 39 more genes
    nsv7057588inversion1nstd229human GRCh38 chr5: 150,061,299-150,061,394 , GRCh37.p13 chr5: 149,440,862-149,440,957 CSF1R
    nsv7053998inversion1nstd229human GRCh38 chr5: 148,749,982-154,424,819 , GRCh37.p13 chr5: 148,129,545-153,804,379 HMGXB3, RN7SL868P, 102 more genes
    nsv7053584inversion1nstd229human GRCh38 chr5: 144,534,922-150,861,041 , GRCh37.p13 chr5: 143,914,485-150,240,603 SMIM3, NAMPTP2, 102 more genes
    nsv7045608inversion1nstd229human GRCh38 chr5: 142,902,498-151,105,008 , GRCh37.p13 chr5: 142,282,063-150,484,569 FBXO38-DT, POU4F3, 126 more genes
    nsv7038217inversion1nstd229human GRCh38 chr5: 142,898,166-151,101,968 , GRCh37.p13 chr5: 142,277,731-150,481,529 RPS20P4, PPARGC1B, 126 more genes
    nsv6796491copy number variation1nstd229human GRCh38 chr5: 150,062,178-150,062,604 , GRCh37.p13 chr5: 149,441,741-149,442,167 CSF1R
    nsv6787108copy number variation1nstd229human GRCh38 chr5: 150,099,411-150,099,459 , GRCh37.p13 chr5: 149,478,974-149,479,022 CSF1R
    nsv6785787copy number variation1nstd229human GRCh38 chr5: 150,049,666-150,064,103 , GRCh37.p13 chr5: 149,429,229-149,443,666 HMGXB3, CSF1R
    nsv6785735copy number variation1nstd229human GRCh38 chr5: 150,084,367-150,084,455 , GRCh37.p13 chr5: 149,463,930-149,464,018 CSF1R
    nsv6785642copy number variation1nstd229human GRCh38 chr5: 150,027,719-150,112,134 , GRCh37.p13 chr5: 149,407,282-149,491,697 PDGFRB, RPL7P1, 2 more genes
    nsv6781687copy number variation1nstd229human GRCh38 chr5: 150,098,406-150,110,516 , GRCh37.p13 chr5: 149,477,969-149,490,079 CSF1R
    nsv6779060copy number variation1nstd229human GRCh38 chr5: 150,054,452-150,054,690 , GRCh37.p13 chr5: 149,434,015-149,434,253 CSF1R
    nsv6564990inversion1nstd223human GRCh38 chr5: 150,093,141-150,093,860 , GRCh37.p13 chr5: 149,472,704-149,473,423 RPL7P1, CSF1R
    nsv6564455inversion1nstd223human GRCh38 chr5: 150,093,047-150,093,784 , GRCh37.p13 chr5: 149,472,610-149,473,347 RPL7P1, CSF1R
    nsv6405162copy number variation1nstd223human GRCh38 chr5: 150,062,175-150,062,600 , GRCh37.p13 chr5: 149,441,738-149,442,163 CSF1R
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6186035copy number variation1nstd214human GRCh38 chr5: 150,084,380-150,084,466 , GRCh37.p13 chr5: 149,463,943-149,464,029 CSF1R
    nsv6184907copy number variation1nstd214human GRCh38 chr5: 150,084,368-150,084,466 , GRCh37.p13 chr5: 149,463,931-149,464,029 CSF1R
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