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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7058053inversion1nstd229human GRCh38 chr6: 12,061,960-18,307,388 , GRCh37.p13 chr6: 12,062,193-18,307,619 RNU7-133P, CAP2, 87 more genes
    nsv7052250inversion1nstd229human GRCh38 chr6: 11,964,842-17,051,222 , GRCh37.p13 chr6: 11,965,075-17,051,453 LINC02543, ARPC3P5, 66 more genes
    nsv7051552inversion1nstd229human GRCh38 chr6: 11,086,774-14,472,374 , GRCh37.p13 chr6: 11,087,007-14,472,605 LOC105374933, ADTRP, 53 more genes
    nsv7042745inversion1nstd229human GRCh38 chr6: 13,249,961-13,338,515 , GRCh37.p13 chr6: 13,250,193-13,338,747 LOC100130357, TBC1D7, 2 more genes
    nsv6791003copy number variation1nstd229human GRCh38 chr6: 13,307,593-13,307,931 , GRCh37.p13 chr6: 13,307,825-13,308,163 TBC1D7, TBC1D7-LOC100130357
    nsv6778396copy number variation1nstd229human GRCh38 chr6: 13,240,748-15,495,244 , GRCh37.p13 chr6: 13,240,980-15,495,475 MRPL35P1, LOC105374938, 34 more genes
    nsv6778371copy number variation1nstd229human GRCh38 chr6: 13,156,197-13,311,343 , GRCh37.p13 chr6: 13,156,429-13,311,575 LOC100130357, LOC105374933, 4 more genes
    nsv6636333copy number variation1nstd102humanPathogenic GRCh37 chr6: 12,005,630-22,849,647 , GRCh38.p12 chr6: 12,005,397-22,849,418 SOX4, MDH1P2, 136 more genes
    nsv6565072inversion1nstd223human GRCh38 chr6: 11,964,842-17,051,222 , GRCh37.p13 chr6: 11,965,075-17,051,453 GMPR, LOC105374933, 66 more genes
    nsv6413950copy number variation1nstd223human GRCh38 chr6: 13,307,593-13,307,931 , GRCh37.p13 chr6: 13,307,825-13,308,163 TBC1D7-LOC100130357, TBC1D7
    nsv6402828copy number variation1nstd223human GRCh38 chr6: 13,156,197-13,311,343 , GRCh37.p13 chr6: 13,156,429-13,311,575 PHACTR1, TBC1D7-LOC100130357, 4 more genes
    nsv6312551copy number variation1nstd102humanUncertain significance GRCh37 chr6: 12,290,863-13,612,097 , GRCh38.p12 chr6: 12,290,630-13,611,865 LOC105374938, LOC105374935, 20 more genes
    nsv6281478insertion2nstd214human GRCh38 chr6: 13,328,502-13,328,502 , GRCh37.p13 chr6: 13,328,734-13,328,734 TBC1D7, TBC1D7-LOC100130357
    nsv6135469copy number variation1nstd213human GRCh37 chr6: 11,730,000-19,840,001 , GRCh38.p12 chr6: 11,729,767-19,839,770 EDN1, GMPR, 115 more genes
    nsv5966298insertion1nstd209human GRCh38 chr6: 13,310,637-13,310,637 , GRCh37.p13 chr6: 13,310,869-13,310,869 TBC1D7-LOC100130357, TBC1D7
    nsv5958327insertion1nstd209human GRCh38 chr6: 13,328,502-13,328,502 , GRCh37.p13 chr6: 13,328,734-13,328,734 TBC1D7, TBC1D7-LOC100130357
    nsv5678634mobile element insertion1nstd211human GRCh38 chr6: 13,320,577-13,320,577 , GRCh37.p13 chr6: 13,320,809-13,320,809 TBC1D7-LOC100130357, TBC1D7
    nsv5456374copy number variation1nstd206human GRCh38 chr6: 13,307,588-13,307,931 , GRCh37.p13 chr6: 13,307,820-13,308,163 TBC1D7-LOC100130357, TBC1D7
    nsv5086171mobile element insertion1nstd203human GRCh38 chr6: 13,310,637-13,310,653 , GRCh37.p13 chr6: 13,310,869-13,310,885 TBC1D7, TBC1D7-LOC100130357
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