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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv7096968copy number variation1nstd102humanUncertain significance GRCh37 chr3: 93,772,011-93,845,334 , GRCh38.p12 chr3: 94,053,167-94,126,490 ARL13B, RBBP4P2, 2 more genes
    nsv7096967copy number variation1nstd102humanPathogenic GRCh37 chr3: 93,714,775-93,724,716 , GRCh38.p12 chr3: 93,995,931-94,005,872 ARL13B
    nsv7096966copy number variation1nstd102humanUncertain significance GRCh37 chr3: 93,593,089-93,772,107 , GRCh38.p12 chr3: 93,874,245-94,053,263 PROS1, HSPE1P17, 4 more genes
    nsv7096479copy number variation1nstd102humanUncertain significance GRCh37 chr3: 93,692,478-93,699,346 , GRCh38.p12 chr3: 93,973,634-93,980,502 ARL13B, PROS1, 1 more genes
    nsv7053739inversion1nstd229human GRCh38 chr3: 94,010,015-94,017,764 , GRCh37.p13 chr3: 93,728,859-93,736,608 STX19, ARL13B
    nsv6705187copy number variation1nstd229human GRCh38 chr3: 94,016,373-94,022,160 , GRCh37.p13 chr3: 93,735,217-93,741,004 STX19, ARL13B
    nsv6702847copy number variation1nstd229human GRCh38 chr3: 94,004,922-94,013,612 , GRCh37.p13 chr3: 93,723,766-93,732,456 STX19, ARL13B
    nsv6701191copy number variation1nstd229human GRCh38 chr3: 94,036,513-94,037,405 , GRCh37.p13 chr3: 93,755,357-93,756,249 ARL13B
    nsv6636560copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 93,519,465-94,372,131 , GRCh38.p12 chr3: 93,800,621-94,653,287 PROS1, NSUN3, 10 more genes
    nsv6629325copy number variation1nstd224human GRCh37 chr3: 93,754,191-93,772,081 , GRCh38.p12 chr3: 94,035,347-94,053,237 ARL13B
    nsv6629324copy number variation1nstd224human GRCh37 chr3: 93,593,119-94,679,788 , GRCh38.p12 chr3: 93,874,275-94,960,944 NSUN3, DHFR2, 11 more genes
    nsv6628894copy number variation1nstd224human GRCh37 chr3: 93,754,191-93,772,145 , GRCh38.p12 chr3: 94,035,347-94,053,301 ARL13B
    nsv6543936inversion1nstd223human GRCh38 chr3: 94,038,527-94,039,219 , GRCh37.p13 chr3: 93,757,371-93,758,063 ARL13B
    nsv6536067inversion1nstd223human GRCh38 chr3: 94,038,745-94,039,521 , GRCh37.p13 chr3: 93,757,589-93,758,365 ARL13B
    nsv6372742copy number variation1nstd223human GRCh38 chr3: 94,026,601-94,027,900 , GRCh37.p13 chr3: 93,745,445-93,746,744 STX19, ARL13B
    nsv6367366copy number variation1nstd223human GRCh38 chr3: 94,016,371-94,022,157 , GRCh37.p13 chr3: 93,735,215-93,741,001 ARL13B, STX19
    nsv6364905copy number variation1nstd223human GRCh38 chr3: 94,050,534-94,051,003 , GRCh37.p13 chr3: 93,769,378-93,769,847 ARL13B
    nsv6364871copy number variation1nstd223human GRCh38 chr3: 94,015,401-94,016,500 , GRCh37.p13 chr3: 93,734,245-93,735,344 STX19, ARL13B
    nsv6362746copy number variation1nstd223human GRCh38 chr3: 94,018,805-94,019,236 , GRCh37.p13 chr3: 93,737,649-93,738,080 ARL13B, STX19
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