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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6628889copy number variation1nstd224human GRCh37 chr3: 88,892,638-89,103,302 , GRCh38.p12 chr3: 88,843,488-89,054,152 GAPDHP50, ICE2P2
    nsv6314751copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 72,488,757-99,614,758 , GRCh38.p12 chr3: 72,439,606-99,895,914 AKR1B1P2, COL8A1, 231 more genes
    nsv6291230copy number variation1nstd102humanUncertain significance GRCh37 chr3: 88,159,133-90,502,849 , GRCh38.p12 chr3: 88,109,983-90,453,699 RNU6-712P, NDUFA5P5, 15 more genes
    nsv6135034copy number variation1nstd213human GRCh37 chr3: 88,970,000-89,390,001 , GRCh38.p12 chr3: 88,920,850-89,340,851 EPHA3, ICE2P2, 1 more genes
    nsv6134716copy number variation1nstd213human GRCh37 chr3: 88,980,000-89,500,001 , GRCh38.p12 chr3: 88,930,850-89,450,851 EPHA3, ICE2P2, 1 more genes
    nsv5081777mobile element insertion1nstd203human GRCh38 chr3: 88,950,137-88,950,149 , GRCh37.p13 chr3: 88,999,287-88,999,299 ICE2P2
    nsv4929063copy number variation1nstd200human GRCh38 chr3: 88,900,842-89,001,794 , GRCh37.p13 chr3: 88,949,992-89,050,944 ICE2P2
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4568251inversion1nstd166human GRCh37.p13 chr3: 81,845,861-90,137,796 , GRCh38.p12 chr3: 81,796,710-90,088,646 POU1F1, CHMP2B, 54 more genes
    nsv4379210copy number variation1nstd173human GRCh37 chr3: 87,205,485-89,477,159 , GRCh38.p12 chr3: 87,156,335-89,428,009 ABCF2P1, KRT8P25, 20 more genes
    nsv3966406insertion1nstd168human GRCh38 chr3: 88,923,894-88,989,505 , GRCh37.p13 chr3: 88,973,044-89,038,655 ICE2P2
    nsv3923231copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 76,896,101-89,814,775 , GRCh37 chr3: 76,813,411-89,732,085 , GRCh38 chr3: 76,764,260-89,682,935 EPHA3, GBE1, 80 more genes
    nsv3919352copy number variation1nstd102humanUncertain significance NCBI36 chr3: 87,280,527-89,571,391 , GRCh37.p13 chr3: 87,197,837-89,488,701 , GRCh38.p12 chr3: 87,148,687-89,439,551 CSNKA2IP, MIR4795, 20 more genes
    nsv3916669copy number variation1nstd102humanPathogenic NCBI36 chr3: 74,781,223-89,627,521 , GRCh37 chr3: 74,698,533-89,544,831 , GRCh38 chr3: 74,649,382-89,495,681 LOC105377187, LOC101927374, 109 more genes
    nsv3916461copy number variation1nstd102humanPathogenic GRCh37 chr3: 57,174,452-90,309,110 , NCBI36 chr3: 57,149,492-90,391,800 , GRCh38 chr3: 57,140,424-90,259,960 LOC105377171, HNRNPA3P6, 323 more genes
    nsv3912034copy number variation1nstd102humanPathogenic GRCh38 chr3: 82,912,987-90,179,222 , GRCh37 chr3: 82,962,138-90,228,372 , NCBI36 chr3: 83,044,828-90,311,062 MTATP6P6, SNORA95, 49 more genes
    nsv3911768copy number variation1nstd102humanPathogenic NCBI36 chr3: 73,956,712-90,585,539 , GRCh37 chr3: 73,874,022-90,502,849 , GRCh38 chr3: 73,824,871-90,453,699 RN7SKP284, OR7E121P, 122 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 RPL23AP49, DLEC1, 2875 more genes
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