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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
    nsv6758086copy number variation1nstd229human GRCh38 chr4: 172,674,978-172,679,095 , GRCh37.p13 chr4: 173,596,129-173,600,246 GALNTL6-AS1, GALNTL6
    nsv6756926copy number variation1nstd229human GRCh38 chr4: 172,724,401-172,737,400 , GRCh37.p13 chr4: 173,645,552-173,658,551 GALNTL6-AS1, GALNTL6
    nsv6755983copy number variation1nstd229human GRCh38 chr4: 172,630,601-172,635,100 , GRCh37.p13 chr4: 173,551,752-173,556,251 GALNTL6-AS1, GALNTL6
    nsv6755312copy number variation1nstd229human GRCh38 chr4: 172,718,655-172,718,963 , GRCh37.p13 chr4: 173,639,806-173,640,114 GALNTL6, GALNTL6-AS1
    nsv6754597copy number variation1nstd229human GRCh38 chr4: 172,662,778-172,665,242 , GRCh37.p13 chr4: 173,583,929-173,586,393 GALNTL6-AS1, GALNTL6
    nsv6753217copy number variation1nstd229human GRCh38 chr4: 170,394,754-173,096,756 , GRCh37.p13 chr4: 171,315,905-174,017,907 HSP90AA6P, MIR6082, 14 more genes
    nsv6752097copy number variation1nstd229human GRCh38 chr4: 172,668,091-172,668,458 , GRCh37.p13 chr4: 173,589,242-173,589,609 GALNTL6-AS1, GALNTL6
    nsv6751186copy number variation1nstd229human GRCh38 chr4: 172,615,320-172,643,715 , GRCh37.p13 chr4: 173,536,471-173,564,866 GALNTL6, GALNTL6-AS1
    nsv6750720copy number variation1nstd229human GRCh38 chr4: 172,650,024-172,654,144 , GRCh37.p13 chr4: 173,571,175-173,575,295 GALNTL6, GALNTL6-AS1
    nsv6748691copy number variation1nstd229human GRCh38 chr4: 172,664,701-172,683,500 , GRCh37.p13 chr4: 173,585,852-173,604,651 GALNTL6-AS1, GALNTL6
    nsv6745117copy number variation1nstd229human GRCh38 chr4: 172,625,666-172,628,612 , GRCh37.p13 chr4: 173,546,817-173,549,763 GALNTL6, GALNTL6-AS1
    nsv6744067copy number variation1nstd229human GRCh38 chr4: 172,653,185-172,656,028 , GRCh37.p13 chr4: 173,574,336-173,577,179 GALNTL6-AS1, GALNTL6
    nsv6742206copy number variation1nstd229human GRCh38 chr4: 172,627,801-172,641,900 , GRCh37.p13 chr4: 173,548,952-173,563,051 GALNTL6, GALNTL6-AS1
    nsv6741606copy number variation1nstd229human GRCh38 chr4: 172,652,301-172,662,900 , GRCh37.p13 chr4: 173,573,452-173,584,051 GALNTL6, GALNTL6-AS1
    nsv6741550copy number variation1nstd229human GRCh38 chr4: 172,648,516-172,671,892 , GRCh37.p13 chr4: 173,569,667-173,593,043 GALNTL6-AS1, GALNTL6
    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
    nsv6629632copy number variation1nstd224human GRCh37 chr4: 173,087,249-173,827,147 , GRCh38.p12 chr4: 172,166,098-172,905,996 LOC100506133, GALNTL6-AS1, 1 more genes
    nsv6629585copy number variation1nstd224human GRCh37 chr4: 173,340,994-173,618,055 , GRCh38.p12 chr4: 172,419,843-172,696,904 GALNTL6, GALNTL6-AS1
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