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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
    nsv7046948inversion1nstd229human GRCh38 chr4: 173,130,800-173,132,580 , GRCh37.p13 chr4: 174,051,951-174,053,731 GALNT7-DT
    nsv6752260copy number variation1nstd229human GRCh38 chr4: 173,157,521-173,157,624 , GRCh37.p13 chr4: 174,078,672-174,078,775 GALNT7-DT
    nsv6752111copy number variation1nstd229human GRCh38 chr4: 173,106,578-173,169,266 , GRCh37.p13 chr4: 174,027,729-174,090,417 RN7SL253P, GALNT7-DT, 1 more genes
    nsv6747879copy number variation1nstd229human GRCh38 chr4: 173,148,024-173,152,054 , GRCh37.p13 chr4: 174,069,175-174,073,205 GALNT7-DT
    nsv6746960copy number variation1nstd229human GRCh38 chr4: 173,042,615-173,284,775 , GRCh37.p13 chr4: 173,963,766-174,205,926 MIR548T, RN7SL253P, 2 more genes
    nsv6745081copy number variation1nstd229human GRCh38 chr4: 173,156,667-173,162,291 , GRCh37.p13 chr4: 174,077,818-174,083,442 GALNT7-DT
    nsv6744498copy number variation1nstd229human GRCh38 chr4: 173,142,734-173,143,091 , GRCh37.p13 chr4: 174,063,885-174,064,242 GALNT7-DT
    nsv6741446copy number variation1nstd229human GRCh38 chr4: 173,123,366-173,132,625 , GRCh37.p13 chr4: 174,044,517-174,053,776 GALNT7-DT
    nsv6738310copy number variation1nstd229human GRCh38 chr4: 173,146,164-173,151,928 , GRCh37.p13 chr4: 174,067,315-174,073,079 GALNT7-DT
    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
    nsv6574937inversion1nstd223human GRCh38 chr4: 173,147,226-173,147,968 , GRCh37.p13 chr4: 174,068,377-174,069,119 GALNT7-DT
    nsv6572506inversion1nstd223human GRCh38 chr4: 173,158,645-173,159,007 , GRCh37.p13 chr4: 174,079,796-174,080,158 GALNT7-DT
    nsv6570050inversion1nstd223human GRCh38 chr4: 169,780,525-178,315,900 , GRCh37.p13 chr4: 170,701,676-179,237,054 LOC101928409, LOC100131553, 91 more genes
    nsv6564602inversion1nstd223human GRCh38 chr4: 173,146,383-173,148,049 , GRCh37.p13 chr4: 174,067,534-174,069,200 GALNT7-DT
    nsv6557294inversion1nstd223human GRCh38 chr4: 173,157,932-173,158,671 , GRCh37.p13 chr4: 174,079,083-174,079,822 GALNT7-DT
    nsv6387748copy number variation1nstd223human GRCh38 chr4: 173,148,021-173,152,050 , GRCh37.p13 chr4: 174,069,172-174,073,201 GALNT7-DT
    nsv6377842copy number variation1nstd223human GRCh38 chr4: 168,709,595-174,342,624 , GRCh37.p13 chr4: 169,630,746-175,263,775 LOC105377527, LOC107986203, 64 more genes
    nsv6313729copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,755,174-190,225,765 , GRCh38.p12 chr4: 158,834,022-189,304,611 NAF1, LOC107986200, 336 more genes
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