KRTAP5-5 - dbVar - NCBI

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3891668	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr11: 1,644,465-1,668,480 , GRCh38.p12 chr11\|NT_187657.1: 99,971-121,272 , GRCh38.p12 chr11: 1,623,235-1,647,250 , GRCh38.p12 chr11\|NT_187584.1: 105,472-129,487	KRTAP5-5
nsv3895380	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 1,645,885-1,654,750 , GRCh38.p12 chr11\|NT_187657.1: 101,391-109,989 , GRCh38.p12 chr11: 1,624,655-1,633,520 , GRCh38.p12 chr11\|NT_187584.1: 106,892-115,757	KRTAP5-5
nsv6891487	copy number variation	1	nstd229	human		GRCh38 chr11: 1,623,845-1,633,605 , GRCh37.p13 chr11: 1,645,075-1,654,835	KRTAP5-5
nsv6886352	copy number variation	1	nstd229	human		GRCh38 chr11: 1,624,406-1,631,630 , GRCh37.p13 chr11: 1,645,636-1,652,860	KRTAP5-5
nsv6883413	copy number variation	1	nstd229	human		GRCh38 chr11: 1,628,383-1,628,449 , GRCh37.p13 chr11: 1,649,613-1,649,679	KRTAP5-5
nsv6917532	copy number variation	1	nstd229	human		GRCh38 chr11: 71,582,771-71,582,814 , GRCh37.p13 chr11: 71,293,817-71,293,860	KRTAP5-11
nsv6451671	copy number variation	1	nstd223	human		GRCh38 chr11: 1,623,845-1,633,601 , GRCh37.p13 chr11: 1,645,075-1,654,831	KRTAP5-5
nsv5508473	copy number variation	1	nstd206	human		GRCh38 chr11: 1,623,845-1,633,601 , GRCh37.p13 chr11: 1,645,075-1,654,831	KRTAP5-5
nsv5505222	copy number variation	1	nstd206	human		GRCh38 chr11: 71,582,494-71,582,560 , GRCh37.p13 chr11: 71,293,540-71,293,606	KRTAP5-11
nsv6206094	copy number variation	1	nstd214	human		GRCh38 chr11: 1,629,897-1,629,968 , GRCh37.p13 chr11: 1,651,127-1,651,198	KRTAP5-5
nsv6201390	copy number variation	1	nstd214	human		GRCh38 chr11: 1,629,926-1,629,997 , GRCh37.p13 chr11: 1,651,156-1,651,227	KRTAP5-5
nsv6194384	copy number variation	1	nstd214	human		GRCh38 chr11: 1,628,383-1,628,448 , GRCh37.p13 chr11: 1,649,613-1,649,678	KRTAP5-5
nsv6191781	copy number variation	1	nstd214	human		GRCh38 chr11: 1,630,163-1,630,222 , GRCh37.p13 chr11: 1,651,393-1,651,452	KRTAP5-5
nsv6031279	copy number variation	1	nstd212	human		GRCh38 chr11: 1,630,186-1,630,243 , GRCh37.p13 chr11: 1,651,416-1,651,473	KRTAP5-5
nsv5316617	copy number variation	1	nstd204	human		GRCh38.p13 chr11: 1,623,835-1,633,605 , GRCh37.p13 chr11: 1,645,065-1,654,835	KRTAP5-5
nsv5588250	copy number variation	1	nstd207	human		GRCh38 chr11: 1,628,320-1,628,369 , GRCh37.p13 chr11: 1,649,550-1,649,599	KRTAP5-5
nsv4845104	copy number variation	1	nstd200	human		GRCh37 chr11: 1,645,075-1,654,831 , GRCh38.p12 chr11: 1,623,845-1,633,601 , GRCh38.p12 chr11\|NT_187657.1: 100,581-109,989 , GRCh38.p12 chr11\|NT_187584.1: 106,082-115,838	KRTAP5-5
nsv4843541	copy number variation	1	nstd200	human		GRCh37 chr11: 71,293,540-71,293,606 , GRCh38.p12 chr11: 71,582,494-71,582,560	KRTAP5-11
nsv4198377	copy number variation	1	nstd166	human		GRCh37.p13 chr11: 1,645,075-1,654,831 , GRCh38.p12 chr11\|NT_187584.1: 106,082-115,838 , GRCh38.p12 chr11: 1,623,845-1,633,601 , GRCh38.p12 chr11\|NT_187657.1: 100,581-109,989	KRTAP5-5
nsv4208824	copy number variation	1	nstd166	human		GRCh37.p13 chr11: 71,293,540-71,293,606 , GRCh38.p12 chr11: 71,582,494-71,582,560	KRTAP5-11

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