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Items: 1 to 20 of 184

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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
    nsv7068065inversion1nstd229human GRCh38 chr22: 27,585,838-32,538,391 , GRCh37.p13 chr22: 27,981,799-32,934,377 LOC105372995, NEFH, 147 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
    nsv7031119copy number variation1nstd229human GRCh38 chr22: 30,450,409-30,450,790 , GRCh37.p13 chr22: 30,846,396-30,846,777 LOC105372991, SEC14L3
    nsv7029660copy number variation1nstd229human GRCh38 chr22: 30,471,374-30,473,440 , GRCh37.p13 chr22: 30,867,361-30,869,427 SEC14L3
    nsv7026162copy number variation1nstd229human GRCh38 chr22: 30,467,266-30,467,342 , GRCh37.p13 chr22: 30,863,253-30,863,329 SEC14L3
    nsv7022562copy number variation1nstd229human GRCh38 chr22: 30,471,028-30,497,083 , GRCh37.p13 chr22: 30,867,015-30,893,070 LOC107985579, SDC4P, 2 more genes
    nsv7021803copy number variation1nstd229human GRCh38 chr22: 30,462,495-30,464,519 , GRCh37.p13 chr22: 30,858,482-30,860,506 SEC14L3
    nsv7020792copy number variation1nstd229human GRCh38 chr22: 30,335,406-30,530,242 , GRCh37.p13 chr22: 30,731,395-30,926,229 SEC14L3, SEC14L2, 13 more genes
    nsv7019259copy number variation1nstd229human GRCh38 chr22: 30,441,124-30,526,524 , GRCh37.p13 chr22: 30,837,111-30,922,511 SEC14L4, SDC4P, 4 more genes
    nsv6638056copy number variation1nstd102humanUncertain significance GRCh37 chr22: 30,649,178-31,035,087 , GRCh38.p12 chr22: 30,253,189-30,639,100 GAL3ST1, SDC4P, 22 more genes
    nsv6537528copy number variation1nstd223human GRCh38 chr22: 30,462,495-30,464,519 , GRCh37.p13 chr22: 30,858,482-30,860,506 SEC14L3
    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
    nsv6252069mobile element insertion1nstd215human GRCh38 chr22: 30,465,142-30,465,142 , GRCh37.p13 chr22: 30,861,129-30,861,129 SEC14L3
    nsv6214320copy number variation1nstd214human GRCh38 chr22: 30,454,511-30,454,601 , GRCh37.p13 chr22: 30,850,498-30,850,588 SEC14L3
    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
    nsv6112267insertion1nstd212human GRCh38 chr22: 30,454,543-30,454,543 , GRCh37.p13 chr22: 30,850,530-30,850,530 SEC14L3
    nsv6058963copy number variation1nstd212human GRCh38 chr22: 30,454,865-30,454,931 , GRCh37.p13 chr22: 30,850,852-30,850,918 SEC14L3
    nsv5961219copy number variation1nstd209human GRCh38 chr22: 30,454,865-30,454,930 , GRCh37.p13 chr22: 30,850,852-30,850,917 SEC14L3
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