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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3873698copy number variation1nstd102humanPathogenic GRCh37 chr11: 103,016,481-103,177,263 , GRCh38 chr11: 103,145,752-103,306,534 DYNC2H1
    nsv4455287copy number variation1nstd102humanPathogenic GRCh37 chr11: 103,297,733-103,368,100 , GRCh38.p12 chr11: 103,427,005-103,497,372 DYNC2H1
    nsv6308941copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 103,325,894-103,349,981 , GRCh38.p12 chr11: 103,455,166-103,479,253 DYNC2H1
    nsv7093749copy number variation1nstd102humanPathogenic GRCh37 chr11: 103,039,464-103,041,817 , GRCh38.p12 chr11: 103,168,735-103,171,088 DYNC2H1
    nsv4436539copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 103,016,472-103,177,263 , GRCh38.p12 chr11: 103,145,743-103,306,534 DYNC2H1
    nsv3885849copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 103,173,802-103,187,369 , GRCh38 chr11: 103,303,073-103,316,640 DYNC2H1
    nsv6291187copy number variation1nstd102humanLikely benign GRCh37 chr11: 103,152,267-103,223,201 , GRCh38.p12 chr11: 103,281,538-103,352,473 DYNC2H1
    nsv6137812insertion1nstd102humanBenign GRCh37 chr11: 103,130,763-103,130,763 , GRCh38 chr11: 103,260,034-103,260,034 DYNC2H1
    nsv3895099copy number variation1nstd102humanUncertain significance GRCh37 chr11: 103,205,399-103,256,732 , GRCh38.p12 chr11: 103,334,671-103,386,004 DYNC2H1
    nsv7093906copy number variation1nstd102humanUncertain significance GRCh37 chr11: 103,228,951-103,229,107 , GRCh38.p12 chr11: 103,358,223-103,358,379 DYNC2H1
    nsv4683484copy number variation1nstd102humanUncertain significance GRCh37 chr11: 103,152,908-103,152,958 , GRCh38.p12 chr11: 103,282,179-103,282,229 DYNC2H1
    nsv7093905copy number variation1nstd102humanUncertain significance GRCh37 chr11: 102,980,304-103,194,738 , GRCh38.p12 chr11: 103,109,575-103,324,010 DYNC2H1
    nsv4682471copy number variation1nstd102humanUncertain significance GRCh37 chr11: 103,349,803-103,350,001 , GRCh38.p12 chr11: 103,479,075-103,479,273 DYNC2H1
    nsv6309176copy number variation1nstd102humanUncertain significance GRCh37 chr11: 103,349,803-103,349,981 , GRCh38.p12 chr11: 103,479,075-103,479,253 DYNC2H1
    nsv3899890copy number variation1nstd102humanBenign GRCh37 chr11: 102,922,881-103,203,377 , GRCh38.p12 chr11: 103,052,152-103,332,649 DYNC2H1, DCUN1D5
    nsv3921457copy number variation1nstd102humanUncertain significance NCBI36 chr11: 102,808,892-102,973,328 , GRCh37.p13 chr11: 103,303,682-103,468,118 , GRCh38.p12 chr11: 103,432,954-103,597,390 DYNC2H1, LOC105369463
    nsv4456009copy number variation1nstd102humanPathogenic GRCh37 chr11: 103,200,944-103,454,659 , GRCh38.p12 chr11: 103,330,216-103,583,931 DYNC2H1, MTND1P36, 5 more genes
    nsv3923293copy number variation1nstd102humanPathogenic NCBI36 chr11: 102,704,746-102,946,835 , GRCh37 chr11: 103,199,536-103,441,625 , GRCh38 chr11: 103,328,808-103,570,897 DYNC2H1, MTND1P36, 5 more genes
    nsv4456396copy number variation1nstd102humanPathogenic GRCh37 chr11: 103,128,365-103,282,941 , GRCh38.p12 chr11: 103,257,636-103,412,213 DYNC2H1, MTND1P36, 5 more genes
    nsv4455570copy number variation3nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 103,128,365-103,282,924 , GRCh38.p12 chr11: 103,257,636-103,412,196 DYNC2H1, MTND1P36, 5 more genes
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