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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099189copy number variation1nstd231human GRCh38.p12 chr1: 27,937,767-28,509,967 , GRCh37 chr1: 28,264,278-28,836,479 RCC1, EYA3, 17 more genes
    nsv7044103inversion1nstd229human GRCh38 chr1: 26,905,652-33,050,814 , GRCh37.p13 chr1: 27,232,143-33,516,415 ADGRB2, SNORA16A, 169 more genes
    nsv7043593inversion1nstd229human GRCh38 chr1: 28,265,647-28,304,326 , GRCh37.p13 chr1: 28,592,158-28,630,837 SESN2
    nsv6647884copy number variation1nstd229human GRCh38 chr1: 28,259,709-28,273,351 , GRCh37.p13 chr1: 28,586,220-28,599,862 SESN2
    nsv6626373copy number variation1nstd224human GRCh37 chr1: 28,598,287-28,661,422 , GRCh38.p12 chr1: 28,271,776-28,334,911 , GRCh38.p12 chr1|NW_018654706.1: 65,420-128,555 MED18, SESN2
    nsv6329624copy number variation1nstd223human GRCh38 chr1: 28,248,432-28,258,477 , GRCh37.p13 chr1: 28,574,943-28,584,988 SESN2
    nsv6326563copy number variation1nstd223human GRCh38 chr1: 28,278,034-28,303,687 , GRCh37.p13 chr1: 28,604,545-28,630,198 SESN2
    nsv6313753copy number variation1nstd102humanUncertain significance GRCh37 chr1: 27,543,877-32,819,121 , GRCh38.p12 chr1: 27,217,386-32,353,520 DCDC2B, SNRNP40, 130 more genes
    nsv6290388copy number variation1nstd102humanUncertain significance GRCh37 chr1: 28,493,687-29,242,679 , GRCh38.p12 chr1: 28,167,176-28,916,167 SNORA16A, MED18, 24 more genes
    nsv6241313mobile element insertion1nstd215human GRCh38 chr1: 28,264,721-28,264,721 , GRCh37.p13 chr1: 28,591,232-28,591,232 SESN2
    nsv6133648copy number variation1nstd213human GRCh37 chr1: 23,300,000-28,930,001 , GRCh38.p12 chr1: 22,973,507-28,603,489 RUNX3, CD52, 195 more genes
    nsv5983889copy number variation1nstd212human GRCh38 chr1: 28,255,123-28,261,821 , GRCh37.p13 chr1: 28,581,634-28,588,332 SESN2
    nsv5685403mobile element insertion2nstd211human GRCh38 chr1: 28,271,316-28,271,316 , GRCh37.p13 chr1: 28,597,827-28,597,827 SESN2
    nsv5427686copy number variation1nstd206human GRCh38 chr1: 22,064,395-28,290,354 , GRCh37.p13 chr1: 22,390,888-28,616,865 , NCMAP-DT, 201 more genes
    nsv5397864mobile element insertion1nstd206human GRCh38 chr1: 28,271,316-28,271,367 , GRCh37.p13 chr1: 28,597,827-28,597,878 SESN2
    nsv5380511translocation1nstd200human GRCh38 chr1: 28,269,919-28,269,919 , GRCh38 chr17: 27,973,060-27,973,060 , GRCh37.p13 chr17: 26,300,086-26,300,086 , GRCh37.p13 chr1: 28,596,430-28,596,430 SESN2, LINC01992
    nsv5380500translocation1nstd200human GRCh38 chr17: 27,973,031-27,973,031 , GRCh38 chr1: 28,269,645-28,269,645 , GRCh37.p13 chr1: 28,596,156-28,596,156 , GRCh37.p13 chr17: 26,300,057-26,300,057 SESN2, LINC01992
    nsv5380491translocation1nstd200human GRCh38 chr1: 28,253,780-28,253,780 , GRCh38 chr1: 28,258,476-28,258,476 , GRCh37.p13 chr1: 28,584,987-28,584,987 , GRCh37.p13 chr1: 28,580,291-28,580,291 SESN2
    nsv5350655translocation1nstd200human GRCh38 chr1: 28,269,645-28,269,645 , GRCh38 chr1: 28,269,710-28,269,710 , GRCh37.p13 chr1: 28,596,156-28,596,156 , GRCh37.p13 chr1: 28,596,221-28,596,221 SESN2
    nsv5345766translocation1nstd200human GRCh37 chr1: 28,596,430-28,596,430 , GRCh37 chr17: 26,300,086-26,300,086 , GRCh38.p12 chr1: 28,269,919-28,269,919 , GRCh38.p12 chr17: 27,973,060-27,973,060 , GRCh38.p12 chr1|NW_018654706.1: 63,563-63,563 SESN2, LINC01992
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