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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148112copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,489,453-18,321,582 , GRCh38.p12 chr16: 15,395,596-18,227,725 , GRCh38.p12 chr16|NT_187607.1: 1,053,559-2,659,700 MIR484, NDE1, 37 more genes
    nsv7148105copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,475,455-16,308,356 , GRCh38.p12 chr16: 15,381,598-16,214,499 , GRCh38.p12 chr16|NT_187607.1: 1,039,549-1,872,496 NDE1, RPL15P20, 15 more genes
    nsv7148099copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,125,542-16,388,672 , GRCh38.p12 chr16: 15,031,685-16,294,815 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-1,952,820 LOC100505915, ABCC1, 28 more genes
    nsv7148091copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,853,752-16,666,672 , GRCh38.p12 chr16: 14,759,895-16,572,815 RPL17P40, PKD1P3-NPIPA1, 54 more genes
    nsv7137121copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 14,819,740-16,364,041 , GRCh38.p12 chr16: 14,725,883-16,270,184 , GRCh38.p12 chr16|NT_187607.1: 266,171-1,928,187 ABCC6, ABCC1, 54 more genes
    nsv7099031copy number variation1nstd102humanUncertain significance GRCh38 chr16: 14,683,149-16,205,174 , GRCh37.p13 chr16: 14,777,006-16,299,031 LOC100288162, LOC105371096, 43 more genes
    nsv7098843copy number variation1nstd102humanLikely pathogenic GRCh38 chr16: 14,683,149-16,536,956 , GRCh37.p13 chr16: 14,777,006-16,630,813 ABCC6, ABCC1, 56 more genes
    nsv7093396copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 14,927,709-16,484,731 , GRCh38.p12 chr16: 14,833,852-16,390,874 ABCC6, ABCC1, 50 more genes
    nsv7076232inversion1nstd229human GRCh38 chr16: 14,972,012-15,457,502 , GRCh37.p13 chr16: 15,065,869-15,551,359 MIR3180-4, LOC105371097, 14 more genes
    nsv7067918inversion1nstd229human GRCh38 chr16: 14,867,200-18,528,889 , GRCh37.p13 chr16: 14,961,057-18,540,211 NPIPA1, NDE1, 80 more genes
    nsv7067385inversion1nstd229human GRCh38 chr16: 15,051,408-15,524,165 , GRCh37.p13 chr16: 15,145,265-15,618,022 LOC105371096, MPV17L, 13 more genes
    nsv7066617inversion1nstd229human GRCh38 chr16: 15,099,482-15,834,316 , GRCh37.p13 chr16: 15,193,339-15,928,173 MARF1, NDE1, 16 more genes
    nsv6973095copy number variation1nstd229human GRCh38 chr16: 15,410,308-15,425,824 , GRCh37.p13 chr16: 15,504,165-15,519,681 MPV17L
    nsv6969039copy number variation1nstd229human GRCh38 chr16: 15,407,849-15,409,093 , GRCh37.p13 chr16: 15,501,706-15,502,950 MPV17L
    nsv6967585copy number variation1nstd229human GRCh38 chr16: 14,928,133-16,326,551 , GRCh37.p13 chr16: 15,021,990-16,420,408 NPIPA5, PKD1P6, 39 more genes
    nsv6967133copy number variation1nstd229human GRCh38 chr16: 15,405,954-15,406,885 , GRCh37.p13 chr16: 15,499,811-15,500,742 MPV17L
    nsv6637991copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 15,316,939-18,770,833 , GRCh38.p12 chr16: 15,223,082-18,759,511 ABCC6, ABCC1, 58 more genes
    nsv6637929copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,780,544-16,330,627 , GRCh38.p12 chr16: 14,686,687-16,236,770 , GRCh38.p12 chr16|NT_187607.1: 259,546-1,894,768 LOC102724984, ABCC6P2, 54 more genes
    nsv6637897copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,449,697-16,391,045 , GRCh38.p12 chr16: 15,355,840-16,297,188 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-1,955,193 BMERB1, MYH11, 17 more genes
    nsv6637792copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 14,925,995-16,309,165 , GRCh38.p12 chr16: 14,832,138-16,215,308 , GRCh38.p12 chr16|NT_187607.1: 531,831-1,873,305 ABCC6, ABCC1, 49 more genes
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