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Items: 1 to 20 of 139

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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
    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
    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
    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
    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
    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
    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
    nsv6361963copy number variation1nstd223human GRCh38 chr3: 94,021,473-94,022,356 , GRCh37.p13 chr3: 93,740,317-93,741,200 STX19, ARL13B
    nsv6314876copy number variation1nstd102humanUncertain significance GRCh37 chr3: 93,698,982-93,774,523 , GRCh38.p12 chr3: 93,980,138-94,055,679 HMGN1P7, STX19, 1 more genes
    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
    nsv6311807copy number variation1nstd102humanPathogenic GRCh37 chr3: 93,593,089-93,845,334 , GRCh38.p12 chr3: 93,874,245-94,126,490 PROS1, NSUN3, 7 more genes
    nsv6224127insertion1nstd214human GRCh38 chr3: 94,025,224-94,025,224 , GRCh37.p13 chr3: 93,744,068-93,744,068 STX19, ARL13B
    nsv5550681insertion1nstd206human GRCh38 chr3: 94,025,229-94,025,275 , GRCh37.p13 chr3: 93,744,073-93,744,119 ARL13B, STX19
    nsv4914507copy number variation1nstd200human GRCh38 chr3: 94,018,775-94,019,258 , GRCh37.p13 chr3: 93,737,619-93,738,102 ARL13B, STX19
    nsv4914506copy number variation1nstd200human GRCh38 chr3: 93,991,806-94,228,578 , GRCh37.p13 chr3: 93,710,650-93,947,422 DHFR2, RBBP4P2, 3 more genes
    nsv4911979copy number variation1nstd200human GRCh38 chr3: 94,017,385-94,017,484 , GRCh37.p13 chr3: 93,736,229-93,736,328 STX19, ARL13B
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