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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139435insertion1nstd232human GRCh37.p13 chr16: 203,118-203,118 , GRCh38.p12 chr16: 153,119-153,119 HBZ
    nsv7067503inversion1nstd229human GRCh38 chr16: 125,934-162,861 , GRCh37.p13 chr16: 175,933-212,860 HBZ, HBZP1, 2 more genes
    nsv7063781inversion1nstd229human GRCh38 chr16: 125,805-180,266 , GRCh37.p13 chr16: 175,804-230,265 HBA2, HBA1, 7 more genes
    nsv6977458copy number variation1nstd229human GRCh38 chr16: 151,746-158,262 , GRCh37.p13 chr16: 201,745-208,261 HBZ
    nsv6977423copy number variation1nstd229human GRCh38 chr16: 78,245-166,188 , GRCh37.p13 chr16: 128,244-216,187 HBZP1, LOC107983982, 4 more genes
    nsv6975933copy number variation1nstd229human GRCh38 chr16: 149,862-183,313 , GRCh37.p13 chr16: 199,861-233,312 HBZ, HBAP1, 6 more genes
    nsv6974397copy number variation1nstd229human GRCh38 chr16: 113,074-160,248 , GRCh37.p13 chr16: 163,073-210,247 LOC107983982, NPRL3, 1 more genes
    nsv6970898copy number variation1nstd229human GRCh38 chr16: 103,803-175,838 , GRCh37.p13 chr16: 153,801-225,837 HBA1, HBM, 6 more genes
    nsv6969917copy number variation1nstd229human GRCh38 chr16: 50,980-156,766 , GRCh37.p13 chr16: 100,980-206,765 HBZ, SNRNP25, 4 more genes
    nsv6965859copy number variation1nstd229human GRCh38 chr16: 147,479-151,817 , GRCh37.p13 chr16: 197,478-201,816 HBZ
    nsv6962097copy number variation1nstd229human GRCh38 chr16: 122,985-378,594 , GRCh37.p13 chr16: 172,984-428,594 MRPL28, HBA1, 16 more genes
    nsv6637972copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,881-1,350,186 , GRCh38.p12 chr16: 35,881-1,300,185 MPG, LOC105371038, 78 more genes
    nsv6637711copy number variation1nstd102humanUncertain significance GRCh37 chr16: 106,989-293,949 , GRCh38.p12 chr16: 56,989-243,950 HBQ1, RHBDF1, 13 more genes
    nsv6637290copy number variation1nstd102humanUncertain significance GRCh37 chr16: 204,932-313,258 , GRCh38.p12 chr16: 154,933-263,259 LUC7L, HBA2, 9 more genes
    nsv6634427copy number variation1nstd102humanPathogenic GRCh37 chr16: 111,043-6,627,459 , GRCh38.p12 chr16: 61,045-6,577,458 HBA1, ANTKMT, 312 more genes
    nsv6623568copy number variation1nstd224human GRCh37 chr16: 201,389-231,021 , GRCh38.p12 chr16: 151,390-181,022 HBA1, HBA2, 6 more genes
    nsv6623417copy number variation1nstd224human GRCh37 chr16: 202,930-231,021 , GRCh38.p12 chr16: 152,931-181,022 HBA1, HBA2, 6 more genes
    nsv6623379copy number variation1nstd224human GRCh37 chr16: 180,529-207,930 , GRCh38.p12 chr16: 130,530-157,931 HBZ, NPRL3
    nsv6623368copy number variation1nstd224human GRCh37 chr16: 138,725-381,927 , GRCh38.p12 chr16: 88,726-331,927 ARHGDIG, HBQ1, 14 more genes
    nsv6513647copy number variation1nstd223human GRCh38 chr16: 145,646-151,398 , GRCh37.p13 chr16: 195,645-201,397 HBZ
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