znhit6[All Fields] AND 1[has_clinical] - dbVar

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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
nsv6314371	complex chromosomal rearrangement	2	nstd102	human	Likely pathogenic	GRCh37 chr5: 88,829,562-88,829,562 , GRCh37 chr5: 88,829,564-88,829,564 , GRCh38.p12 chr5: 89,533,745-89,533,745 , GRCh38.p12 chr5: 89,533,747-89,533,747 , GRCh38.p12 chr1: 85,691,448-85,691,448 , GRCh38.p12 chr1: 85,691,449-85,691,449 , GRCh37 chr1: 86,157,131-86,157,131 , GRCh37 chr1: 86,157,132-86,157,132	ZNHIT6
nsv3904449	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr1: 85,900,439-86,431,014 , GRCh37 chr1: 86,127,851-86,658,426 , GRCh38 chr1: 85,662,168-86,192,743	ZNHIT6, LOC105378823, 2 more genes
nsv3901546	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 59,057,865-86,336,882 , GRCh37 chr1: 59,285,277-86,564,294 , GRCh38 chr1: 58,819,605-86,098,611	ZNHIT6, ROR1, 333 more genes
nsv6313574	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 68,180,293-92,731,957 , GRCh38.p12 chr1: 67,714,610-92,266,400	ZNHIT6, RNA5SP51, 315 more genes
nsv3886551	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 64,321,264-88,153,669 , GRCh38.p12 chr1: 63,855,593-87,687,986	ZNHIT6, RNU6-1102P, 291 more genes
nsv3885743	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 72,044,544-92,505,091 , GRCh38.p12 chr1: 71,578,861-92,039,534	ZNHIT6, CCN1, 257 more genes
nsv3905989	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 76,884,987-89,094,147 , NCBI36 chr1: 76,657,575-88,866,735 , GRCh38 chr1: 76,419,302-88,628,464	ZNHIT6, DNAJB4, 146 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	ZNHIT6, MARK1, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	ZNHIT6, SNAP47, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	ZNHIT6, RNU1-153P, 4887 more genes
nsv3898327	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 83,457,325-104,273,917 , GRCh37 chr1: 83,923,008-104,816,539 , NCBI36 chr1: 83,695,596-104,618,062	ZNHIT6, LINC01773, 322 more genes
nsv4728566	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr1: 80,804,502-89,490,384 , GRCh38.p12 chr1: 80,338,817-89,024,701	ZNHIT6, CLCA1, 103 more genes
nsv3871671	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 85,765,619-86,697,145 , GRCh38.p12 chr1: 85,299,936-86,231,462	ZNHIT6, CCN1, 6 more genes
nsv3882306	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr1: 86,006,704-86,727,751 , GRCh38.p12 chr1: 85,541,021-86,262,068	ZNHIT6, DDAH1, 6 more genes
nsv3882974	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr1: 85,761,564-86,703,902 , GRCh38.p12 chr1: 85,295,881-86,238,219	ZNHIT6, RNA5SP51, 6 more genes
nsv4450384	copy number variation	1	nstd102	human	not provided	GRCh37 chr1: 66,085,524-88,429,789 , GRCh38.p12 chr1: 65,619,841-87,964,106	ZNHIT6, DEPDC1, 264 more genes
nsv6637014	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 85,878,203-86,849,716 , GRCh38.p12 chr1: 85,412,520-86,384,033	ZNHIT6, RNA5SP51, 10 more genes
nsv3878920	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 86,027,015-86,606,921 , GRCh38.p12 chr1: 85,561,332-86,141,238	ZNHIT6, CCN1, 6 more genes
nsv4436181	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532	ZNHIT6, LINC01776, 1853 more genes
nsv3910639	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr1: 85,115,279-85,922,965 , GRCh37.p13 chr1: 85,342,691-86,150,377 , GRCh38.p12 chr1: 84,877,008-85,684,694	ZNHIT6, DNAI3, 13 more genes

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Items: 20

Number of Variants: 20

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