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Items: 1 to 20 of 245

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7041510inversion1nstd229human GRCh38 chr5: 73,610,616-81,398,473 , GRCh37.p13 chr5: 72,906,441-80,694,292 LOC105379034, RBMX2P5, 134 more genes
    nsv6776870copy number variation1nstd229human GRCh38 chr5: 80,520,401-80,631,300 , GRCh37.p13 chr5: 79,816,220-79,927,119 ANKRD34B, DHFR, 3 more genes
    nsv6774248copy number variation1nstd229human GRCh38 chr5: 80,507,881-80,512,663 , GRCh37.p13 chr5: 79,803,700-79,808,482 FAM151B
    nsv6768398copy number variation1nstd229human GRCh38 chr5: 80,502,151-80,508,821 , GRCh37.p13 chr5: 79,797,970-79,804,640 FAM151B
    nsv6768092copy number variation1nstd229human GRCh38 chr5: 80,506,939-80,517,489 , GRCh37.p13 chr5: 79,802,758-79,813,308 FAM151B
    nsv6766951copy number variation1nstd229human GRCh38 chr5: 80,535,365-80,544,016 , GRCh37.p13 chr5: 79,831,184-79,839,835 FAM151B
    nsv6760341copy number variation1nstd229human GRCh38 chr5: 79,938,101-80,575,500 , GRCh37.p13 chr5: 79,233,924-79,871,319 RBMX2P5, RPL7P24, 19 more genes
    nsv6572937inversion1nstd223human GRCh38 chr5: 80,511,235-80,511,683 , GRCh37.p13 chr5: 79,807,054-79,807,502 FAM151B
    nsv6571812inversion1nstd223human GRCh38 chr5: 80,496,979-80,497,278 , GRCh37.p13 chr5: 79,792,798-79,793,097 RPS27AP9, FAM151B
    nsv6556478inversion1nstd223human GRCh38 chr5: 80,520,657-80,521,055 , GRCh37.p13 chr5: 79,816,476-79,816,874 FAM151B
    nsv6397977copy number variation1nstd223human GRCh38 chr5: 80,507,881-80,512,661 , GRCh37.p13 chr5: 79,803,700-79,808,480 FAM151B
    nsv6395719copy number variation1nstd223human GRCh38 chr5: 80,516,087-80,517,980 , GRCh37.p13 chr5: 79,811,906-79,813,799 FAM151B
    nsv6281956insertion1nstd214human GRCh38 chr5: 80,529,907-80,529,907 , GRCh37.p13 chr5: 79,825,726-79,825,726 FAM151B
    nsv6244436mobile element insertion1nstd215human GRCh38 chr5: 80,503,693-80,503,693 , GRCh37.p13 chr5: 79,799,512-79,799,512 FAM151B
    nsv6244435mobile element insertion1nstd215human GRCh38 chr5: 80,501,486-80,501,486 , GRCh37.p13 chr5: 79,797,305-79,797,305 RPL7P24, FAM151B
    nsv6165677copy number variation1nstd214human GRCh38 chr5: 80,538,437-80,538,486 , GRCh37.p13 chr5: 79,834,256-79,834,305 FAM151B
    nsv6164268copy number variation1nstd214human GRCh38 chr5: 80,538,425-80,538,486 , GRCh37.p13 chr5: 79,834,244-79,834,305 FAM151B
    nsv6141099copy number variation1nstd206human GRCh38 chr5: 80,529,907-80,529,967 , GRCh37.p13 chr5: 79,825,726-79,825,786 FAM151B
    nsv6135683copy number variation1nstd213human GRCh37 chr5: 76,940,000-80,890,001 , GRCh38.p12 chr5: 77,644,175-81,594,182 ACTBP2, ARSB, 63 more genes
    nsv6135437copy number variation1nstd213human GRCh37 chr5: 78,580,000-80,500,001 , GRCh38.p12 chr5: 79,284,177-81,204,182 DBIP2, DHFR, 40 more genes
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