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Items: 1 to 20 of 222

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5624213insertion1nstd207human GRCh38 chr3: 94,043,620-94,043,620 , GRCh37.p13 chr3: 93,762,464-93,762,464 ARL13B
    nsv5619673insertion1nstd207human GRCh38 chr3: 94,043,558-94,043,558 , GRCh37.p13 chr3: 93,762,402-93,762,402 ARL13B
    nsv5605675insertion1nstd207human GRCh38 chr3: 94,043,553-94,043,553 , GRCh37.p13 chr3: 93,762,397-93,762,397 ARL13B
    nsv5550681insertion1nstd206human GRCh38 chr3: 94,025,229-94,025,275 , GRCh37.p13 chr3: 93,744,073-93,744,119 ARL13B, STX19
    nsv5381424copy number variation1nstd102humanUncertain significance GRCh37 chr3: 93,768,230-93,772,107 , GRCh38.p12 chr3: 94,049,386-94,053,263 ARL13B
    nsv5306019copy number variation1nstd204human GRCh37.p13 chr3: 93,702,800-93,705,115 , GRCh38.p13 chr3: 93,983,956-93,986,271 ARL13B, HMGN1P7
    nsv5239452copy number variation1nstd204human GRCh38.p13 chr3: 93,983,907-93,986,297 , GRCh37.p13 chr3: 93,702,751-93,705,141 ARL13B, HMGN1P7
    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
    nsv4911978copy number variation1nstd200human GRCh38 chr3: 93,983,966-93,986,267 , GRCh37.p13 chr3: 93,702,810-93,705,111 ARL13B, HMGN1P7
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4797508copy number variation1nstd200human GRCh37 chr3: 93,769,379-93,769,847 , GRCh38.p12 chr3: 94,050,535-94,051,003 ARL13B
    nsv4797507copy number variation1nstd200human GRCh37 chr3: 93,740,287-93,741,190 , GRCh38.p12 chr3: 94,021,443-94,022,346 STX19, ARL13B
    nsv4797506copy number variation1nstd200human GRCh37 chr3: 93,702,810-93,705,111 , GRCh38.p12 chr3: 93,983,966-93,986,267 ARL13B, HMGN1P7
    nsv4759793insertion1nstd199human GRCh37 chr3: 93,762,382-93,762,382 , GRCh38.p12 chr3: 94,043,538-94,043,538 ARL13B
    nsv4704840copy number variation1nstd195human GRCh37 chr3: 93,674,351-93,791,651 , GRCh38.p12 chr3: 93,955,507-94,072,807 PROS1, NSUN3, 5 more genes
    nsv4701731copy number variation1nstd195human GRCh37 chr3: 93,674,651-93,954,451 , GRCh38.p12 chr3: 93,955,807-94,235,607 PROS1, NSUN3, 6 more genes
    nsv4682065copy number variation1nstd102humanUncertain significance GRCh37 chr3: 93,754,175-93,780,355 , GRCh38.p12 chr3: 94,035,331-94,061,511 ARL13B, DHFR2, 1 more genes
    nsv4681867copy number variation1nstd102humanUncertain significance GRCh37 chr3: 93,692,518-93,845,334 , GRCh38.p12 chr3: 93,973,674-94,126,490 RNU6-511P, NSUN3, 6 more genes
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