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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7078067inversion1nstd229human GRCh38 chr22: 30,287,061-38,012,264 , GRCh37.p13 chr22: 30,683,050-38,408,271 LINC02885, RN7SL20P, 203 more genes
    nsv7065500inversion1nstd229human GRCh38 chr22: 29,260,563-37,652,385 , GRCh37.p13 chr22: 29,656,552-38,048,392 RFPL1, PATZ1, 217 more genes
    nsv7036509copy number variation1nstd229human GRCh38 chr22: 32,858,001-32,863,000 , GRCh37.p13 chr22: 33,253,988-33,258,987 TIMP3, SYN3
    nsv7035262copy number variation1nstd229human GRCh38 chr22: 32,821,065-32,821,257 , GRCh37.p13 chr22: 33,217,051-33,217,243 TIMP3, SYN3
    nsv7032602copy number variation1nstd229human GRCh38 chr22: 32,831,378-32,833,903 , GRCh37.p13 chr22: 33,227,364-33,229,889 SYN3, TIMP3
    nsv7032020copy number variation1nstd229human GRCh38 chr22: 32,809,246-32,810,421 , GRCh37.p13 chr22: 33,205,232-33,206,407 SYN3, TIMP3
    nsv7021371copy number variation1nstd229human GRCh38 chr22: 32,836,758-33,010,060 , GRCh37.p13 chr22: 33,232,745-33,406,045 SYN3, TIMP3
    nsv6596874inversion1nstd223human GRCh38 chr22: 32,737,340-34,823,587 , GRCh37.p13 chr22: 33,133,326-35,219,578 LINC01643, LOC441996, 14 more genes
    nsv6554505copy number variation1nstd223human GRCh38 chr22: 32,846,452-32,847,258 , GRCh37.p13 chr22: 33,242,439-33,243,245 TIMP3, SYN3
    nsv6553242copy number variation1nstd223human GRCh38 chr22: 32,826,994-32,827,675 , GRCh37.p13 chr22: 33,222,980-33,223,661 TIMP3, SYN3
    nsv6551800copy number variation1nstd223human GRCh38 chr22: 32,851,677-32,852,200 , GRCh37.p13 chr22: 33,247,664-33,248,187 SYN3, TIMP3
    nsv6551126copy number variation1nstd223human GRCh38 chr22: 32,831,376-32,833,900 , GRCh37.p13 chr22: 33,227,362-33,229,886 TIMP3, SYN3
    nsv6537097copy number variation1nstd223human GRCh38 chr22: 32,852,005-32,872,737 , GRCh37.p13 chr22: 33,247,992-33,268,724 TIMP3, SYN3
    nsv6311321copy number variation1nstd102humanUncertain significance GRCh37 chr22: 32,232,938-34,157,463 , GRCh38.p12 chr22: 31,836,952-33,761,476 SYN3, DEPDC5, 36 more genes
    nsv6311263copy number variation1nstd102humanUncertain significance GRCh37 chr22: 29,083,885-34,046,674 , GRCh38.p12 chr22: 28,687,897-33,650,688 SNORD125, LOC107985533, 145 more genes
    nsv6285787insertion1nstd214human GRCh38 chr22: 32,814,337-32,814,337 , GRCh37.p13 chr22: 33,210,323-33,210,323 SYN3, TIMP3
    nsv6146327copy number variation1nstd206human GRCh38 chr22: 32,843,972-32,844,023 , GRCh37.p13 chr22: 33,239,959-33,240,010 TIMP3, SYN3
    nsv6134210copy number variation1nstd213human GRCh37 chr22: 30,130,000-36,350,001 , GRCh38.p12 chr22: 29,734,011-35,953,953 HMOX1, LIF, 146 more genes
    nsv6134118copy number variation1nstd213human GRCh37 chr22: 27,870,000-35,640,001 , GRCh38.p12 chr22: 27,474,039-35,244,008 AP1B1, EWSR1, 172 more genes
    nsv6106772insertion1nstd212human GRCh38 chr22: 32,814,324-32,814,324 , GRCh37.p13 chr22: 33,210,310-33,210,310 SYN3, TIMP3
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