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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1398410copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 76,905,697-76,967,064 , GRCh38 chr14: 76,439,354-76,500,721 ESRRB
    nsv7093074copy number variation1nstd102humanLikely benign GRCh37 chr14: 76,966,423-76,966,490 , GRCh38 chr14: 76,500,080-76,500,147 ESRRB
    nsv3901424copy number variation1nstd102humanLikely benign GRCh37 chr14: 76,837,541-77,007,569 , GRCh38.p12 chr14: 76,371,198-76,541,226 ESRRB
    nsv3893981copy number variation1nstd102humanLikely benign GRCh37 chr14: 76,837,541-76,957,445 , GRCh38.p12 chr14: 76,371,198-76,491,102 ESRRB
    nsv3879472copy number variation1nstd102humanBenign GRCh37 chr1: 217,162,443-217,207,089 , GRCh38.p12 chr1: 216,989,101-217,033,747 ESRRG
    nsv6290523copy number variation1nstd102humanUncertain significance GRCh37 chr1: 216,859,478-217,324,311 , GRCh38.p12 chr1: 216,686,136-217,150,969 ESRRG
    nsv3913590copy number variation1nstd102humanUncertain significance NCBI36 chr14: 75,899,611-76,116,324 , GRCh37.p13 chr14: 76,829,858-77,046,571 , GRCh38.p12 chr14: 76,363,515-76,580,228 ESRRB
    nsv4451864copy number variation1nstd102humanUncertain significance GRCh37 chr1: 217,157,107-217,206,596 , GRCh38.p12 chr1: 216,983,765-217,033,254 ESRRG
    nsv4455240copy number variation1nstd102humanUncertain significance GRCh37 chr14: 76,931,560-76,977,846 , GRCh38.p12 chr14: 76,465,217-76,511,503 ESRRB
    nsv5673250copy number variation1nstd102humanPathogenic GRCh37 chr1: 216,348,580-216,896,641 , GRCh38.p12 chr1: 216,175,238-216,723,299 ESRRG, USH2A, 3 more genes
    nsv6314407complex chromosomal rearrangement2nstd102humanUncertain significance GRCh37 chr5: 93,556,332-93,556,332 , GRCh37 chr5: 93,556,663-93,556,663 , GRCh38.p12 chr5: 94,220,627-94,220,627 , GRCh38.p12 chr5: 94,220,958-94,220,958 , GRCh38.p12 chr1: 216,778,780-216,778,780 , GRCh38.p12 chr1: 216,779,771-216,779,771 , GRCh37 chr1: 216,952,122-216,952,122 , GRCh37 chr1: 216,953,113-216,953,113 ESRRG, KIAA0825, 1 more genes
    nsv3896513copy number variation1nstd102humanPathogenic NCBI36 chr1: 214,636,660-215,789,771 , GRCh37 chr1: 216,570,037-217,723,148 , GRCh38 chr1: 216,396,695-217,549,806 ESRRG, USH2A, 4 more genes
    nsv3910270copy number variation1nstd102humanPathogenic GRCh38 chr13: 18,445,862-114,327,173 , NCBI36 chr13: 10,098,739-114,110,750 , GRCh37 chr13: 19,020,001-115,085,141 RNU6-71P, LINC00676, 1332 more genes
    nsv3905232copy number variation1nstd102humanPathogenic GRCh38 chr3: 32,241-12,681,483 , GRCh37 chr3: 73,914-12,722,982 , NCBI36 chr3: 48,914-12,697,982 OR7E122P, SRGAP3, 163 more genes
    nsv3885461copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-12,575,409 , GRCh38.p12 chr3: 20,213-12,533,910 MARK2P14, RN7SL147P, 160 more genes
    nsv3923727copy number variation1nstd102humanPathogenic GRCh37 chr14: 70,028,816-82,441,728 , GRCh38 chr14: 69,562,099-81,975,384 , NCBI36 chr14: 69,098,569-81,511,481 CEP128, COX6CP11, 240 more genes
    nsv6636276copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,892-11,679,509 , GRCh38.p12 chr3: 20,214-11,638,035 RPL23AP39, LOC107986059, 144 more genes
    nsv3906827copy number variation1nstd102humanPathogenic GRCh38 chr3: 32,241-11,379,835 , GRCh37 chr3: 73,914-11,421,309 , NCBI36 chr3: 48,914-11,396,309 LOC107986040, EGOT, 142 more genes
    nsv3895550copy number variation1nstd102humanPathogenic GRCh38 chr3: 20,213-11,221,602 , NCBI36 chr3: 36,891-11,238,288 , GRCh37 chr3: 61,891-11,263,288 SRGAP3, LOC101927394, 141 more genes
    nsv3900952copy number variation1nstd102humanPathogenic GRCh38 chr3: 52,266-11,089,569 , NCBI36 chr3: 68,949-11,106,255 , GRCh37 chr3: 93,949-11,131,255 RPUSD3, RPS8P6, 137 more genes
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