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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099260copy number variation1nstd231human GRCh38.p12 chr1: 207,518,788-210,916,265 , GRCh37 chr1: 207,692,133-211,089,607 ADORA2BP1, ATP5MC2P1, 60 more genes
    nsv7095569copy number variation2nstd102humanUncertain significance GRCh37 chr1: 200,522,516-208,391,267 , GRCh38.p12 chr1: 200,553,388-208,217,922 TRK-TTT8-1, ADIPOR1, 228 more genes
    nsv7044092inversion1nstd229human GRCh38 chr1: 203,118,726-211,305,271 , GRCh37.p13 chr1: 203,087,854-211,478,613 LOC100420418, LINC00260, 201 more genes
    nsv6668938copy number variation1nstd229human GRCh38 chr1: 207,806,429-207,812,724 , GRCh37.p13 chr1: 207,979,774-207,986,069 MIR29B2CHG
    nsv6660220copy number variation1nstd229human GRCh38 chr1: 207,738,001-208,652,200 , GRCh37.p13 chr1: 207,911,346-208,825,545 LOC105372887, LOC105372884, 14 more genes
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6554773inversion1nstd223human GRCh38 chr1: 204,500,842-208,290,127 , GRCh37.p13 chr1: 204,469,970-208,463,472 RNA5SP75, LOC105372869, 108 more genes
    nsv6322033copy number variation1nstd223human GRCh38 chr1: 207,806,429-207,812,718 , GRCh37.p13 chr1: 207,979,774-207,986,063 MIR29B2CHG
    nsv6310745copy number variation2nstd102humanUncertain significance GRCh37 chr1: 206,941,981-208,391,267 , GRCh38.p12 chr1: 206,768,636-208,217,922 PFKFB2, LOC105372878, 39 more genes
    nsv6298267copy number variation1nstd186human GRCh37 chr1: 207,983,204-207,983,417 , GRCh38.p12 chr1: 207,809,859-207,810,072 MIR29B2CHG
    nsv6162265copy number variation1nstd214human GRCh38 chr1: 207,818,308-207,818,357 , GRCh37.p13 chr1: 207,991,653-207,991,702 MIR29B2CHG, LOC148696
    nsv6133752copy number variation1nstd213human GRCh37 chr1: 207,160,000-210,270,001 , GRCh38.p12 chr1: 206,986,655-210,096,656 ADORA2BP1, C4BPA, 62 more genes
    nsv6133630copy number variation2nstd213human GRCh37 chr1: 206,490,000-223,720,001 , GRCh38.p12 chr1: 206,316,655-223,546,636 ATP5MC2P1, CENPF, 269 more genes
    nsv5982295copy number variation1nstd212human GRCh38 chr1: 207,818,307-207,818,362 , GRCh37.p13 chr1: 207,991,652-207,991,707 LOC148696, MIR29B2CHG
    nsv5449971copy number variation1nstd206human GRCh38 chr1: 207,809,859-207,810,072 , GRCh37.p13 chr1: 207,983,204-207,983,417 MIR29B2CHG
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5329500translocation1nstd204human GRCh38.p13 chr1: 194,772,506-194,772,506 , GRCh38.p13 chr1: 207,801,893-207,801,893 , GRCh37.p13 chr1: 194,741,636-194,741,636 , GRCh37.p13 chr1: 207,975,238-207,975,238 MIR29B2, MIR29C, 1 more genes
    nsv4898409copy number variation1nstd200human GRCh38 chr1: 207,809,859-207,810,072 , GRCh37.p13 chr1: 207,983,204-207,983,417 MIR29B2CHG
    nsv4898408copy number variation1nstd200human GRCh38 chr1: 207,806,429-207,812,718 , GRCh37.p13 chr1: 207,979,774-207,986,063 MIR29B2CHG
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