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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112794copy number variation1nstd102humanPathogenic GRCh37 chr22: 50,099,570-51,187,115 , GRCh38.p12 chr22: 49,705,922-50,748,687 SCO2, CIMAP1B, 50 more genes
    nsv5968901inversion1nstd209human GRCh38 chr2: 237,879,581-237,879,674 , GRCh37.p13 chr2: 238,788,223-238,788,316 RAMP1
    nsv5963603insertion1nstd209human GRCh38 chr7: 93,460,568-93,460,568 , GRCh37.p13 chr7: 93,089,880-93,089,880 CALCR
    nsv5954595insertion1nstd209human GRCh38 chr2: 237,908,410-237,908,410 , GRCh37.p13 chr2: 238,817,052-238,817,052 RAMP1
    nsv5953615insertion1nstd209human GRCh38 chr7: 93,517,298-93,517,298 , GRCh37.p13 chr7: 93,146,610-93,146,610 CALCR
    nsv5950138insertion1nstd209human GRCh38 chr7: 93,532,838-93,532,838 , GRCh37.p13 chr7: 93,162,150-93,162,150 LOC105375400, CALCR
    nsv5926397copy number variation1nstd209human GRCh38 chr7: 45,161,872-45,163,913 , GRCh37.p13 chr7: 45,201,471-45,203,512 RAMP3
    nsv5926233copy number variation1nstd209human GRCh38 chr7: 93,555,382-93,556,747 , GRCh37.p13 chr7: 93,184,694-93,186,059 CALCR, LOC105375400
    nsv5917459copy number variation1nstd209human GRCh38 chr7: 93,531,551-93,593,896 , GRCh37.p13 chr7: 93,160,863-93,223,208 LOC105375400, CALCR
    nsv5916949copy number variation1nstd209human GRCh38 chr7: 93,526,415-93,526,467 , GRCh37.p13 chr7: 93,155,727-93,155,779 CALCR
    nsv5910891copy number variation1nstd209human GRCh38 chr7: 93,540,675-93,540,790 , GRCh37.p13 chr7: 93,169,987-93,170,102 CALCR, LOC105375400
    nsv5899627copy number variation1nstd209human GRCh38 chr2: 187,350,991-187,351,297 , GRCh37.p13 chr2: 188,215,718-188,216,024 CALCRL, CALCRL-AS1
    nsv5897436copy number variation1nstd209human GRCh38 chr2: 237,869,111-237,869,257 , GRCh37.p13 chr2: 238,777,754-238,777,900 RAMP1
    nsv5889266copy number variation1nstd209human GRCh38 chr2: 187,366,086-187,375,134 , GRCh37.p13 chr2: 188,230,813-188,239,861 CALCRL, CALCRL-AS1
    nsv5867416copy number variation1nstd209human GRCh38 chr7: 93,541,304-93,546,003 , GRCh37.p13 chr7: 93,170,616-93,175,315 LOC105375400, CALCR
    nsv5862522copy number variation1nstd209human GRCh38 chr7: 93,531,577-93,540,403 , GRCh37.p13 chr7: 93,160,889-93,169,715 LOC105375400, CALCR
    nsv5860016copy number variation2nstd209human GRCh38 chr7: 93,554,973-93,556,796 , GRCh37.p13 chr7: 93,184,285-93,186,108 CALCR, LOC105375400
    nsv5850448copy number variation1nstd209human GRCh38 chr7: 93,546,991-93,593,008 , GRCh37.p13 chr7: 93,176,303-93,222,320 CALCR, LOC105375400
    nsv5832825copy number variation2nstd209human GRCh38 chr2: 237,886,562-237,887,661 , GRCh37.p13 chr2: 238,795,204-238,796,303 RAMP1
    nsv5832311copy number variation2nstd209human GRCh38 chr2: 187,365,987-187,375,299 , GRCh37.p13 chr2: 188,230,714-188,240,026 CALCRL, CALCRL-AS1
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