essv6685957 - dbVar - NCBI

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Items: 4

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Number of Variants: 4

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
esv2718938	copy number variation	31	estd201	human		GRCh37 chr19: 55,544,145-55,544,971 , GRCh38.p12 chr19\|NT_187693.1: 1,015,259-1,016,085 , GRCh38.p12 chr19\|NW_003571061.2: 744,938-745,764 , GRCh38.p12 chr19\|NW_003571057.2: 1,040,300-1,041,126 , GRCh38.p12 chr19\|NW_003571059.2: 951,142-951,968 , GRCh38.p12 chr19: 55,032,777-55,033,603 , GRCh38.p12 chr19\|NW_003571056.2: 1,012,763-1,013,589 , GRCh38.p12 chr19\|NW_003571055.2: 677,979-678,805 , GRCh38.p12 chr19\|NW_003571060.1: 935,559-936,385 , GRCh38.p12 chr19\|NW_003571058.2: 1,014,849-1,015,675 , GRCh38.p12 chr19\|NW_003571054.1: 936,175-937,001	GP6, GP6-AS1
esv2718937	copy number variation	22	estd201	human		GRCh37 chr19: 55,544,098-55,544,716 , GRCh38.p12 chr19\|NW_003571060.1: 935,512-936,130 , GRCh38.p12 chr19: 55,032,730-55,033,348 , GRCh38.p12 chr19\|NW_003571056.2: 1,012,716-1,013,334 , GRCh38.p12 chr19\|NW_003571055.2: 677,932-678,550 , GRCh38.p12 chr19\|NW_003571057.2: 1,040,253-1,040,871 , GRCh38.p12 chr19\|NW_003571059.2: 951,095-951,713 , GRCh38.p12 chr19\|NT_187693.1: 1,015,212-1,015,830 , GRCh38.p12 chr19\|NW_003571061.2: 744,891-745,509 , GRCh38.p12 chr19\|NW_003571058.2: 1,014,802-1,015,420 , GRCh38.p12 chr19\|NW_003571054.1: 936,128-936,746	GP6-AS1, GP6
esv2718941	copy number variation	28	estd201	human		GRCh37 chr19: 55,544,294-55,544,716 , GRCh38.p12 chr19\|NW_003571061.2: 745,087-745,509 , GRCh38.p12 chr19\|NW_003571055.2: 678,128-678,550 , GRCh38.p12 chr19: 55,032,926-55,033,348 , GRCh38.p12 chr19\|NT_187693.1: 1,015,408-1,015,830 , GRCh38.p12 chr19\|NW_003571060.1: 935,708-936,130 , GRCh38.p12 chr19\|NW_003571056.2: 1,012,912-1,013,334 , GRCh38.p12 chr19\|NW_003571057.2: 1,040,449-1,040,871 , GRCh38.p12 chr19\|NW_003571058.2: 1,014,998-1,015,420 , GRCh38.p12 chr19\|NW_003571059.2: 951,291-951,713 , GRCh38.p12 chr19\|NW_003571054.1: 936,324-936,746	GP6, GP6-AS1
esv2718872	copy number variation	693	estd201	human		GRCh37 chr19: 54,983,739-55,605,615 , GRCh38.p12 chr19: 54,472,594-54,911,985 , GRCh38.p12 chr19\|NT_187693.1: 454,853-894,467 , GRCh38.p12 chr19\|NW_003571054.1: 379,006-987,716 , GRCh38.p12 chr19\|NW_003571060.1: 377,247-987,100 , GRCh38.p12 chr19\|NW_003571061.2: 363,080-796,479 , GRCh38.p12 chr19\|NW_003571055.2: 399,097-729,520	VN1R105P, RNU6-222P, 41 more genes

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