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Items: 1 to 20 of 145

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050217inversion1nstd229human GRCh38 chr2: 24,022,162-24,022,273 , GRCh37.p13 chr2: 24,245,032-24,245,143 MFSD2B
    nsv7044373inversion1nstd229human GRCh38 chr2: 24,017,921-24,022,363 , GRCh37.p13 chr2: 24,240,791-24,245,233 MFSD2B
    nsv6676890copy number variation1nstd229human GRCh38 chr2: 23,963,439-24,043,304 , GRCh37.p13 chr2: 24,186,309-24,266,174 FKBP1B, RN7SL610P, 3 more genes
    nsv6675892copy number variation1nstd229human GRCh38 chr2: 24,009,810-24,019,506 , GRCh37.p13 chr2: 24,232,680-24,242,376 MFSD2B
    nsv6666873copy number variation1nstd229human GRCh38 chr2: 23,622,207-24,033,282 , GRCh37.p13 chr2: 23,845,077-24,256,152 SDHCP3, KLHL29, 8 more genes
    nsv6663543copy number variation1nstd229human GRCh38 chr2: 23,871,801-24,132,500 , GRCh37.p13 chr2: 24,094,671-24,355,370 SF3B6, WDCP, 12 more genes
    nsv6637009copy number variation1nstd102humanUncertain significance GRCh37 chr2: 23,908,436-24,636,185 , GRCh38.p12 chr2: 23,685,566-24,413,316 HMGN2P20, KLHL29, 19 more genes
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6550111inversion1nstd223human GRCh38 chr2: 24,012,330-24,015,385 , GRCh37.p13 chr2: 24,235,200-24,238,255 MFSD2B
    nsv6355161copy number variation1nstd223human GRCh38 chr2: 24,020,077-24,022,508 , GRCh37.p13 chr2: 24,242,947-24,245,378 MFSD2B
    nsv6354916copy number variation1nstd223human GRCh38 chr2: 23,986,421-24,044,996 , GRCh37.p13 chr2: 24,209,291-24,267,866 FKBP1B, MFSD2B, 4 more genes
    nsv6347214copy number variation1nstd223human GRCh38 chr2: 24,016,029-24,019,988 , GRCh37.p13 chr2: 24,238,899-24,242,858 MFSD2B
    nsv6337325copy number variation1nstd223human GRCh38 chr2: 23,963,253-24,089,139 , GRCh37.p13 chr2: 24,186,123-24,312,009 FAM228B, FKBP1B, 7 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314937copy number variation1nstd102humanPathogenic GRCh37 chr2: 22,439,520-25,608,211 , GRCh38.p12 chr2: 22,216,648-25,385,342 ITSN2, POMC, 50 more genes
    nsv5451088copy number variation1nstd206human GRCh38 chr2: 24,009,891-24,009,958 , GRCh37.p13 chr2: 24,232,761-24,232,828 MFSD2B
    nsv5061756mobile element insertion1nstd203human GRCh38 chr2: 24,012,170-24,012,179 , GRCh37.p13 chr2: 24,235,040-24,235,049 MFSD2B
    nsv4904851copy number variation1nstd200human GRCh38 chr2: 24,027,222-24,031,809 , GRCh37.p13 chr2: 24,250,092-24,254,679 WDCP, MFSD2B, 1 more genes
    nsv4900642copy number variation1nstd200human GRCh38 chr2: 24,020,142-24,022,502 , GRCh37.p13 chr2: 24,243,012-24,245,372 MFSD2B
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